Abstract
Adolescents with intellectual disability have a right to sexuality education, including relationships and consent education. This scoping review explored relationships and consent education for adolescents with intellectual disability. We searched across four databases (Scopus, Medline, Web of Science and PubMed) to identify studies focusing on the provision of, experiences with and needs of education on relationships and consent for adolescents aged 12–19 with intellectual disability. Based on the inclusion criteria, 20 studies were eligible to be included in the review. The findings suggest that despite adolescents’ strong desire for comprehensive, evidence-based education on relationships and consent, the depth and content of the education provided varied by the provider type. Many educators and parents felt unprepared to address complex relationship and consent topics, resulting in inconsistent and often risk-focused education. The review indicated the need for more tailored resources, engaged learning methods, increased training and support for providers, and collaborative approaches between different providers. Future consent and relationships education could benefit from moving from a risk-based approach to focus on personal development and the promotion of sexual well-being for adolescents with intellectual disability.
1. Introduction
Sexuality education is an inalienable right for all adolescents, including those with intellectual disability (). The major internationally accepted human rights bodies, including the United Nations Convention on the Rights of the Child, the Convention on the Elimination of All Forms of Discrimination against Women, and the United Nations Convention on the Rights of Persons with Disabilities, have acknowledged these rights (; ; , , ). Relationships and consent are key concepts recommended by UNESCO under comprehensive sexuality education curricula (; ). UNESCO’s international technical guidance on sexuality education covers relationships as Key Concept 1, addressing families, friendship, love, romantic relationships, tolerance, inclusion, respect, long-term commitments, and parenting. Consent, privacy, and bodily integrity fall under Key Concept 4, focusing on violence and safety. This concept highlights the importance of understanding and respecting these rights while communicating boundaries within relationships (; ). Relationships and consent education are now mandatory in primary and secondary school curricula in several countries, including Australia, the UK, Ireland, and Canada. These topics are typically taught by Health and Physical Education teachers and are often integrated into sexuality education or programs aimed at preventing gender-based violence ().
Adolescence is a crucial life stage for learning and understanding the development of relationships and consent (). According to the World Health Organization (WHO), “Adolescence is the phase of life between childhood and adulthood, from ages 10 to 19. It is a unique stage of human development and an important time for laying the foundations of good health” (). Good quality and developmentally appropriate CSE, including relationships and consent, is one of the vital elements of adolescent health interventions ().
Adolescents with intellectual disability have similar sexual desires to those of other adolescents. An intellectual disability is the limitation of intellectual functioning that occurs before, during, or shortly after birth and is life-long. It affects mild, moderate, severe or profound cognitive impairment, particularly in learning, problem-solving, judgement, self-care and communication (; ). Despite increased awareness and international pledges to advance the sexual and reproductive health of people with intellectual disability, they have inadequate access to sexuality education and information (). Their sexuality is often overlooked and described as challenging (). The sexual autonomy and well-being of these adolescents are not frequently recognised (). For young people with disabilities, CSE is a powerful tool that empowers them to seek help and make informed, respectful choices about relationships, sexuality, and health (; ). CSE equips adolescents, including those with intellectual disability, with accurate, age-appropriate knowledge, positive values, and skills to maintain healthy relationships. It also encourages reflection on social norms and cultural values, helping young people navigate emotions, power imbalances, and relationships with peers, parents and others. A rights-based approach in CSE boosts awareness of sexual rights, improves communication about relationships, and enhances confidence in managing risky situations, leading to better psychosocial well-being and positive behavioural changes (; ).
However, systemic barriers, including insufficient content of the relationship and sexuality education programs by the teachers and the lack of accessible resources, inhibit access to relationships and sexuality education for individuals with intellectual disability (; ). Due to cognitive and communication barriers, some may not be able to understand others’ intentions and approaches, recognise disinterest, maintain boundaries or communicate rejection in romantic relationships. They still need support to develop practical skills for navigating relationships, understanding consent, and communicating a firm yes or no in a relationship (; ; ). Specialised education on respectful relationships, dating, consent and boundaries, communication skills, and consensual sexual activity within a disability-specific context is essential. However, little is known about what adolescents with intellectual disability know about relationships and consent and how they acquire this knowledge. There are a number of providers of this education, but evidence about the challenges and barriers they experience and the resources available to them is scarce (). To understand the complexity surrounding the relationships and consent education of adolescents with intellectual disability, it is crucial to consider the views of adolescents and the people who care for them (; ).
This review maps the existing literature on the provision of, experiences with and needs for relationships and consent education for adolescents aged 12–19 with intellectual disability (‘adolescents’ thereafter). We aimed to describe: 1. What adolescents know and would like to know about relationships and consent, how they acquire that knowledge; 2. The content of relationships and consent education currently delivered to adolescents by education and care providers (‘providers’ thereafter); 3. The self-perceived competence of providers in delivering relationships and consent education; and 4. Barriers and enablers in the provision of relationship and consent education and resources available to providers.
2. Materials and Methods
We undertook a scoping review guided by the methodological framework established by () and Joanna Briggs Institute (JBI) guidance (). This review’s reporting follows the criteria set out in the PRISMA-ScR 2018 (Preferred Reporting Items for Systematic Reviews and Meta-Analyses Extension for Scoping Reviews) guidelines (). The research questions were formulated using the Population, Concept, and Context framework according to JBI guidance ().
This review focuses on key concepts related to relationships and consent, as outlined in UNESCO guidance: relationships; values, rights, culture and sexuality; violence and staying safe; skills for health and well-being; and sexuality and sexual behaviour ().
2.1. Literature Search Strategy
A systematic search of primary peer-reviewed publications was conducted in Scopus, Web of Science, Ovid (MEDLINE), and PubMed in July 2024. We used key terms related to relationships and consent education to identify relevant literature and combined them into a search formula with Boolean terms (AND and OR) and wild cards. The following formula was used for search in Scopus:
TITLE-ABS-KEY (((sex* OR consent OR relationship) AND (education)) AND ((adolescen* OR students OR young AND people OR youth OR pubescen* OR teenager*) AND (intellectual AND disability))) AND PUBYEAR > 2010 AND PUBYEAR < 2025 AND (LIMIT-TO (LANGUAGE, “English”)).
Similar search terms and strategies were adapted to other databases. Citation chaining (backward and forward) was performed on identified publications to maximise search results.
2.2. Selection of Publication
This review’s population of interest is adolescents with intellectual disability (with or without autism) aged 12–19 and their parents, teachers, disability and healthcare providers. Pre-defined inclusion and exclusion criteria guided the screening of identified articles. Included were original peer-reviewed articles; articles published in English from 2010 inclusive; studies conducted in high- and middle-income countries; studies of any design including program descriptions (excluding case reports, editorials, opinion papers, and reviews of any type); studies reporting on adolescents with intellectual disability with or without other conditions such as autism spectrum disorder or other multiple disabilities, and studies where samples included adolescents aged 12–19 or their parents, teachers, healthcare providers, disability providers and/or carers. Included were studies focused on relationships and consent education, including current knowledge, desired knowledge, knowledge acquisition, content delivered, educator competence, barriers, and supports. Excluded were studies that reported on adolescents with autism spectrum disorder and other multiple disabilities without intellectual disability, covered broader age ranges and did not allow data extraction specifically for the 12–19 age group, and studies presenting combined analyses for paediatric populations and adults alongside the 12–19 age group. Following the search, all identified citations were imported into the Covidence systematic review software (Veritas Health Innovation; https://www.covidence.org/, accessed on 23 October 2024), and duplicates were removed. The selection process included three steps: two reviewers performed primary screening of titles, abstracts, and full text for eligibility. The third reviewer resolved disagreements between the two reviewers.
2.3. Charting the Data/Data Extraction
Data were extracted into Microsoft Excel. We extracted details about the study, participants, concept, context, study methods, and key findings relevant to the review questions. The following variables were extracted from the studies: publication description (author, year of publication, country of research), study design, education setting, disability status, study focus, sample description (population groups, sample size), content on relationships and consent, and key results in relation to the research questions.
2.4. Data Analysis and Presentation
Key concepts and themes were created using a thematic analysis approach (). To address possible bias, the research team reviewed, confirmed, and reached a consensus on the final themes (; ). We followed the Key concept areas recommended by the International Technical Guidance on Sexuality Education (). Of the eight topic areas recommended by UNESCO, we selected five that were relevant to this study. These included: 1. Relationships; 2. Values, rights, culture and sexuality; 4. Violence and staying safe; 5. Skills for health and well-being; and 7. Sexuality and sexual behaviour.
3. Results
3.1. Literature Search Results
As demonstrated in Figure 1, we identified 1126 literature records: 386 in Web of Science, 335 in Scopus, 267 in PubMed, 104 in Medline and 34 via citation chaining. After removing 261 duplicates via Covidence, we screened 865 unique titles and abstracts.
Figure 1.
PRISMA flowchart of literature search. Adapted from Covidence.
From the title and abstract screening, we excluded 823 publications. We assessed the full text of 42 studies against our inclusion and exclusion criteria and excluded 22 papers. Reasons for exclusion were: a different topic focus, a different population (adult or paediatric), an excluded study design, or a year of publication before 2010. Twenty studies met the inclusion criteria and were retained in this review.
3.2. Summary of the Studies/Characteristics of Included Publications
Table 1 summarises the characteristics of the included papers. The research presented in the selected papers was conducted in 11 countries, with the majority (n = 6) in the United States. The rest of the research was from Canada (n = 2), Australia (n = 2), the United Kingdom (n = 2), Germany (n = 2), Latvia (n = 1), Ireland (n = 1), Turkey (n = 1), Lithuania (n = 1), Brazil (n = 1), and Sweden (n = 1). Three papers were published between 2012 and 2014 (; ; ), six were published between 2015 and 2018 (; ; ; ; ; ) and over 50% (n = 11) of the studies were published in the past five years (2019–2024) (; ; ; ; ; ; ; , ; ; ).
Table 1.
Characteristics of the published papers included in the review.
The research methods varied, including 13 studies of qualitative design (interviews, focus groups, and observations (; ; ; ; ; ; ; ; ; ; , ; ); two with mixed methods (; ); two program descriptions (; ); and one study, each employing curriculum evaluation (), a quantitative study design (), and a quasi-experimental approach ().
Ten studies specifically focused on adolescents with intellectual disabilities (; ; ; ; ; ; ; ; ; ), six on adolescents with intellectual disability and other conditions, including autism spectrum disorder (; ; ; ; ; ), and four included mixed groups of adolescents and young adults with intellectual disability and sometimes with other multiple conditions (; ; ). Seven publications described home-based educational settings (; ; ; ; ; ; ), seven school-based settings (; ; ; ; ; ; ), and six mixed settings (homes, schools, and institutions) (; ; ; ; ; ). Among the mixed settings, one study focused on accommodation and day centre providers (), another on a child rehabilitation centre (), and another at a mental health clinic where clinicians trained adolescents in personal safety with parental support ().
The reviewed studies focused on various aspects of sexuality and relationships for individuals with intellectual disabilities, such as how relationship and sexuality education (RSE) is provided and perceived by different stakeholders, including carers, professionals and educators (; ; ); parental involvement (; ; ); curriculum development and evaluation (; ; ); consent and autonomy (; ); sexual abuse prevention () and lived experiences of individuals with intellectual disability, including caregivers’ perspectives (; , ).
3.3. What Adolescents Know and Would Like to Know About Relationships and Consent, How They Acquire That Knowledge
Table 2 describes our findings on what adolescents currently know and what they would like to know about relationships and consent. Adolescents expressed a desire to receive accurate (), evidence-based (), age-appropriate () information that can provide a foundational understanding of concepts before moving to complex topics (). Overall, they would like to receive comprehensive sex education (; ).
Table 2.
What adolescents currently know and would like to know about relationships and consent.
Adolescents had limited access to education on relationships and consent. They often lack having a trusted adult to discuss these topics (). Informal sources of information frequently lack depth (). Home-based education by parents and caregivers was often reactive and based on inquiries (; ). Parents, especially mothers, struggled with family communication and sharing information about sexuality, relationships, and consent (; ). Consequently, family education was often patchy and inadequate (; ). Parents of adolescents recognised the need for more structured education () and individualised, interactive, sensory-friendly resources tailored to their needs (; ).
School-based relationships and consent education are often inconsistent. While some programs, like the Ask Me First Choices program, a four-module sexual consent intervention specifically designed for use with students receiving special education services in the USA (), are well-structured and education in this area is generally seen as inadequate and reliant on caregivers (). The reviewed publications highlighted a need for structured curricula tailored to adolescents with intellectual disability (), adaptable to their learning needs (), and with ongoing monitoring of their understanding (). Successful programs should include appropriate educational materials, visual aids, role plays, and formative assessments ().
There has been minimal research on relationships and consent education in clinical settings. Only () described a community mental health clinic program providing tailored education and personal safety training for adolescents with intellectual disability.
Adolescents with intellectual disability primarily learn about relationships and consent from parents, teachers, and via observation. They also rely on external sources (). Their values, attitudes and cultural beliefs are influenced by the information they receive from peers, media and social observation (; ; ). In a Canadian study by Heifetz et al., adolescents gained better romantic awareness from social observation, peers, and media than learning from their parents (). Most adolescents learned about romantic relationships from their parents, highlighting potential gaps in formal sex education. Discussing relationships with parents did not correlate with advanced dating stages, as adolescents viewed relationships as lifelong commitments focused on companionship (). Some adolescents held traditional views on gender roles, linking happiness to heterosexual relationships, marriage and personal living space (). This suggests the need for education distinguishing romantic relationships from friendships, covering their roles, the diversity of sexuality, and the right to enjoy sexual pleasure and protect oneself from sexual abuse ().
Research suggests that education at home and school is more effective when provided concurrently and in agreement (). This approach includes traditional instruction, workshops, video demonstrations, storybook readings, discussions, and take-home assignments for parental reinforcement (; ; ; ; ).
3.4. Content of Education Delivered to Adolescents by Education and Care Providers
Table 3 describes topics in relationships and consent education that are being delivered to adolescents by provider type. The relationship and consent education provided to adolescents varies by provider type. Parents covered the foundational, practical, and ethical aspects of relationships, focusing on safety, consent, and personal rights. Key topics included building friendships, dating safety, communication skills, safe boundaries (; ), and public versus private behaviour (; ). They addressed managing relationships, understanding “no”, touching rules and personal space (). Consent, boundaries, appropriate sexual behaviour (; ; ), and the respectful initiation and ending of relationships were highlighted ().
Table 3.
Relationships and consent education topics being delivered to adolescents by provider type.
Parents also covered cultural beliefs and social norms, including ethical considerations (; ), human rights as to sexuality and privacy (), and the roles and responsibilities within family structures related to friendships and relationships (; ). Emotional connections and types of romantic relationships were discussed (), though deeper romantic topics were often avoided (). Some parents emphasised long-term commitments, hopes for their children’s lasting relationships, capacity for intimacy, and partner selection, but these topics were not explicitly taught as part of educational content (; ; , ). Parents sought guidance and support to effectively cover these aspects of relationship education.
Teachers provided a structured educational framework focusing on social skills, relationship dynamics, understanding emotions, consent, communication, and safe behaviours with varying comfort levels and details. Key concepts included friendships and how they can evolve into romance, dating dynamics and emotional implications (; ), positive and negative aspects of relationships (), public versus private behaviour (), basic safety principles, and consent (; ; ; ). Two studies investigated the inclusion of self-awareness, self-advocacy and self-determination in the educational content and highlighted that few teachers covered these topics (; ). Teachers introduced concepts of sexual consent, decision-making strategies, communication of consent and resources for sexual abuse support (; ) while also developing social skills and understanding peer pressure and societal norms (). Family dynamics, diverse family values, and anti-bullying content were integrated into the curriculum, although sexual behaviour content was often covered reactively following incidents (). Personal beliefs, inclusivity and respect, safe online behaviour, and support resources were emphasised (; ; ; ).
Healthcare and disability providers focused on empowering adolescents to recognise and respond to inappropriate behaviours, emphasising skills development for their health and well-being (; ; ; ). The clinician-led education curricula focused on consent and personal boundaries (), including identifying appropriate versus inappropriate touches, understanding one’s body, and developing safety skills. Other topics were effective communication, refusal of unwanted advances, and negotiation skills, which parents can reinforce at home. The program also covered recognising adult helpers, such as parents, school staff, relatives, professionals, and peers (). Some healthcare providers emphasised a human rights perspective for adolescents with intellectual disability, but education offered on these topics was limited (). Clinicians often focused on legal and safety requirements rather than personal development () and did not include topics on relationships, values, culture and sexuality (; ).
Educators from the disability services covered body privacy and safety, family roles, safe and unsafe friendships, appropriate boundaries, and consent (). Key areas included respecting personal space, acceptance in friendships, self-respect, body parts, good versus bad touch, and personal rights regarding one’s body. Children learned their right to privacy and safety, how to say “no” to unwanted touching and communicate discomfort and seek help, including asking for assistance from family members during health examinations (). Special education teachers, youth workers, and outreach workers covered personal values and their impact on decision-making, including sexual rights, consent, bodily autonomy, appropriate behaviours, and healthy relationships (). Key areas included managing sexual anxiety, setting boundaries, making informed choices, and developing effective communication, assertiveness, and negotiation skills ().
3.5. The Self-Perceived Competence of Education and Care Providers in Providing Relationships and Consent Education
Many teachers and family carers feel ill-equipped in providing relationships and consent education due to a lack of formal training () but were aware of the challenges (; ). Some showed mixed feelings of empowerment and uncertainty (; ). Some teachers felt confident in basic topics but relied on external professionals for complex issues (). Special education teachers in the USA demonstrated varying confidence levels and expressed an interest in training on Universal Design for Learning principles (). Parents delivered education based on their knowledge and comfort rather than formal training (). Mothers lacked confidence and were anxious to discuss sensitive topics (; ; ). Clinicians, on the other hand, did not explicitly state their self-perceived competence ().
In a positive light, some educators and parents used structured approaches to education, indicating high competence levels (). Some schoolteachers felt competent, in general, but faced challenges with nonverbal students (), while others highlighted varying levels of self-perceived competence, particularly in emotional and relationship education, and difficulty assessing comprehension (; ). They also knew where to find information on sexuality education ().
Teaching Methods Used or Preferred by Providers
Current teaching methods differed among providers. Two program intervention studies emphasised using the Universal Design for Learning principle, including the use of reference aids, visual instructions, case studies, role play, small group discussions, videos and take-home assignments (; ; ). These studies also advocated for extension activities and Treatment and Education of Autistic and related Communication-handicapped children (TEACCH) methods, including practical intervention guides with questions and answers (; ). Some teachers and family carers commonly used advocacy groups, peer tutors, and person-centred plans, recommending gender-specific courses provided through gender-homogeneous groups and gender-specific educators (; ; ). Some also used effective strategies like the Stein and Glen Story Map Method to write a series of stories and picture books to teach adolescents about sexual abuse. Similarly, homework rewards, positive reinforcement and modelling, and interactive multimodal teaching tools like drama, vignettes, scenarios, and social stories were effectively used (; ; ; ; ).
School teachers used well-developed guidelines and pedagogical methods, including tiered and spiral curricula and recommended age-appropriate learning and consistent vocabulary (; ; ). They used individualised learning plans, and tailored programs like the ‘Circles program’, which teaches adolescents about personal boundaries, consent, and protective behaviours, by helping them to identify the circles of people in their life and different roles and rules in their relationships with family, friends and strangers (). Some teachers also used Mind maps, formative assessment over formal assessment, breaking content down via content adjustment, exit slips and Know Want Learned charts, which help students organise information before, during, and after learning about a topic (). Parents were more likely to use the reactive teaching approach, often waiting for the adolescents to start the conversation (; ; ; ). Clinicians providing training at mental health clinics also used vignettes, short-answer questions, scenarios and recommended formative assessments focusing on in-session tasks (). Providers also preferred proactive, inclusive, and tailored teaching methods with various multimodal teaching approaches ().
3.6. Barriers, Enablers and Resources Available to Education and Care Providers Regarding Relationship and Consent
3.6.1. Barriers
The lack of training and support in delivering relationship and consent education was perceived as a key barrier across different education and care providers (; ; ; ; ). There is a scarcity of educational resources and comprehensive educational materials (; ; ; ; ; ; ; ) that are tailored to the needs of individuals with intellectual disability, age-appropriate (; ; ; ; ), and culturally and linguistically appropriate (). Cultural and societal attitudes, including personal and religious beliefs, may affect educators’ comfort and willingness to teach sexuality content and hinder open discussion. Family attitudes, including the perceived socio-sexual inadequacy of individuals with intellectual disability, myths and fears about their sexuality, stigma and perceived vulnerability and the perception of heterosexual bias were some of the barriers identified in several reviewed studies (; ; ; ).
Communication challenges were significant (; ; ). Parents struggled to establish effective communication with their children. Cognitive limitations and varying social competence levels make it hard for individuals with intellectual disability to understand abstract relationship concepts (; ; ; ; ), often requiring repeated explanations (; ). Teachers found it challenging to assess comprehension and adjust teaching methods for mixed-ability students (; ). Therefore, parents and teachers often felt discomfort and reluctance to discuss complex relationship topics (; ; ).
Schoolteachers commonly reported inconsistent educational practices, including insufficient guidelines, gaps in socio-sexuality curricula, and inconsistent implementation across schools (; ; ; ). Parents similarly perceived a gap in structured sexuality education and noted minimal interaction with teachers on relationship-related topics (; ). Parents felt that limited social opportunities, including a lack of privacy, mobility issues, cultural expectations, exclusion from social activities and social isolation, prevented their adolescents from learning how to navigate friendships and relationships in practice (; , )
3.6.2. Enablers
Professional frontline staff, families, clinicians and teachers emphasised that accessible information and training facilitated relationship and consent education and requested further training on relevant legislation and resource development (; ; ; ). Providers would like to have resources that are accessible, relevant, trusted, and appropriate to the developmental and diverse learning needs of adolescents with intellectual disability. They wanted resources that are interactive and multi-lingual (; ; ; ; ; ; ; ; ; ; ), mixed training sessions for parents and children (), individualised learning plans, visuals, role plays, and tailored storybooks (; ). Providers would like to be able to use a range of formats, such as books (; ; ; ), structured curriculum activities (; ; ; ), illustrations (; ), informational tools (; ; ; ; ), theatre performances (), videos (; ; ; ) and visual aids (; ; ; ).
Some parents and teachers used engaging learning methods, including relatable content, interest-driven learning, repetitive learning methods, supportive small group discussions, persistent reinforcement strategies and proactive approaches to teaching about sexuality (; ; ). Creating supportive educational environments and inclusive social opportunities for social interaction was valued (; , ). Some teachers involved external professionals, such as psychologists, to cover sensitive topics to avoid discomfort (). Special education teachers were more likely than other providers to seek professional development in sexual education and were aware of where to seek assistance (). Some studies used collaborative approaches, including community-based partnerships and support among schools, families, healthcare providers and disability professionals (; ; ; ). Education was more effective when parents were strongly involved and provided insights on physical safety skills (). Education and support groups for parents (; ; ; ; ; ) and professional advice and support from paediatricians were recommended ().
4. Discussion
This review identified several important findings. First, adolescents had a limited understanding of relationships and consent, but they wanted happy relationships and were interested in learning more about how to achieve them. Second, education content varied significantly by provider type, and each provider’s methods varied. Third, most providers generally felt confident covering basic topics but identified a need for improved communication methods and increased support and training in various areas of relationships and consent conversations. Finally, the recommendations for improvement included increased training, the use of engaging methods, active parental involvement, provider collaboration, and improved communication and customised resources.
Most of the studies we reviewed found that adolescents had a varied and patchy understanding of relationship topics (; ) such as awareness of relationship evolution (; ; , ), but their understanding of the complex dynamics of a relationship, including respect and the nuances of consent, was often limited (; ; ). Their understanding of sexual behaviours, emotional connections (), and regulations () varied with inadequate practical strategies to manage emotions (). Awareness and skills regarding personal safety (; ), including internet safety (), were shallow and often influenced by misinformation from the media (). Their understanding of relationships, gender roles, commitment and marriage was often traditional and heterosexually biased (; ). These findings are not surprising in the context where the sexuality of adolescents with an intellectual disability is often overlooked, and their access to sexuality education and information is inadequate (; ). Our findings highlight the need to provide adolescents with social opportunities and appropriate media access ().
Despite their limited understanding, many adolescents seemed optimistic about relationships and strongly desired accurate, evidence-based, and age-appropriate information (; ; ). They sought foundational knowledge on building healthy and happy relationships (; ; ; ; ; ; ) and how to incorporate consent in relationship dynamics (; ; ; ; ; ; ; ; ). Of specific interest to adolescents were skills for safety and well-being in relationships, including effective communication (; ), decision-making (), online safety (; ), emotional regulation and emotional intelligence (; ; ), navigating romantic and relationship challenges, including managing breakups () and healthy relationship dynamics (). Their desire for relationships and interest in learning more about healthy relationships could help adolescents learn about their topics of interest (). One major issue for many adolescents was a lack of a trusted adult in their lives to share concerns and receive information and advice, and, in their absence, adolescents had to resort to informal and external sources of information that often lacked depth and reliability ().
Education content varied significantly by provider type. Parents generally offered foundational, ethical, and practical aspects, emphasising safety, cultural values, and social norms. Parents’ education was often based on personal experiences and tended to be heterosexually biased and focused on long-term commitment. Some parents expressed scepticism about their children’s future relationships (; ; ; ; ; ; ; ; , ; ). Teachers provided more structured education, focusing on relationship concepts, social skills, communication, decision-making strategies, safe behaviours, anti-bullying, online safety, and peer pressure (; ; ; ; ; ; ; ; ). The level of detail and comfort in delivering education varied, but parents and teachers seemed to complement each other in this effort. Healthcare and disability providers focused on empowerment and safety skills for adolescents’ health and well-being, including negotiation skills and finding support, with reinforcement at home. Some healthcare providers emphasised legal and safety requirements over personal development, and it was unclear if they covered relationships, values, culture, and sexuality (; ). Some disability providers, however, used a social and tailored approach to address individual learning needs ().
Relationship and consent education was included in school curricula but was often inadequate and inconsistent (). While some well-structured school programs existed (; ), they were not always tailored to the diverse learning needs of adolescents with intellectual disability (). There was a significant gap in formal education distinguishing between romantic relationships and friendships (). Traditional views on gender roles, heterosexual relationships and marriage () suggest a need for broader education on diverse sexualities and sexual rights. Previous studies also highlighted that existing education at schools and homes was inadequate, often conservative, negatively framed, and focused on heteronormativity messages, which can lead to social exclusion by preventing adolescents from experiencing their rights to sexuality (; ; ). Similarly, most education from parents, carers and some health professionals focused on risk-based and protectionist approaches to education (), which overlooked the positive aspects of relationships and sexuality. This aligns with previous studies suggesting that positive aspects of sexuality are generally underexplored, especially for adolescents with intellectual disability (; ; ; ; ). Some studies indicated that sexual health education provided to adolescents with an intellectual disability was limited to preventing abuse, vulnerability or pregnancy rather than sex-positive approaches to relationships and intimacy and recommended for disability-specific content with aspects of pleasure and desire (; ; ; ; ; ; ). Future consent and relationships education could benefit from moving from a risk-based approach to one that promotes personal development and sexual well-being for adolescents with intellectual disability ().
In addition to education content, teaching methods differed among providers. Parents used reactive and sporadic approaches, often waiting for the adolescents to start the conversation (; ; ), but recognised a need for clear, explicit conversation and enhanced support and resources for parents (; ; ; ). School education was based on well-developed guidelines and pedagogical methods, including tiered and spiral curricula, individual learning plans (; ; ) and tailored programs. Some successful examples, such as the ‘Circles’ () and ‘Ask Me First Choices’ () programs, deserved further implementation research. Healthcare providers and clinicians employed professional and scenarios-based teaching methods using vignettes and scenarios typically used in clinical education (; ; ).
Despite various techniques used, all providers indicated a lack of formal training, which was often a reason for a lack of confidence in providing relationship and consent education. Many teachers and family carers generally felt ill-equipped () but were aware of the challenges (; ). Parents, especially mothers, seemed anxious discussing sensitive topics (; ; ; ) and provided education drawing from their personal experience and comfort levels, seeking more guidance and support. Teachers showed mixed feelings of empowerment and uncertainty (; ). Those using structured approaches demonstrated higher competence (), while others highlighted varying confidence levels, particularly in emotional and relationship education. One of the challenges for teachers was difficulty assessing comprehension (; ; ) when working with nonverbal students (), indicating a need for extensive training. Clinicians did not explicitly express a lack of competence (), as only two studies specifically addressed clinicians’ perspectives. These studies indicated that some clinicians and frontline staff jointly sought training in policy and practice related to legislation, parenting assessments, and resource development, supported by improved procedures for staff supervision and organisational policies ().
Our review highlights numerous barriers to sexuality and consent education. Some barriers are common, such as inconsistent educational practices (; ; ), lack of training and support for providers (; ; ; ; ; ), and limited resources and materials (; ; ; ; ; ; ; ). Other barriers are specific to adolescents with intellectual disability, such as complexities of topics and content (; ; ; ; ), lack of individualised and customised resources (; ), communication challenges (; ; ; ; ; ) and social isolation of adolescents with intellectual disability (; , ). Further complicating this education are cultural and societal attitudes, which deprive adolescents with intellectual disability (as members of society) of the inherent human right to have healthy and satisfying relationships. Some parents and educators expressed fear of increasing sexual behaviour and avoided discussing relationship topics with adolescents ()—a finding that was reported in previous studies (; ). Combined with assumptions that adolescents with intellectual disability are childlike and asexual, these negative provider views hinder comprehensive education (). We found mixed perspectives, as some parents doubted their adolescents’ future relationships. Parents believed that adolescents should be older before they start dating, compared to what the adolescents thought. A subset of parents felt that adolescents would never be ready for relationships (). Adolescents who discussed relationships with these parents were less likely to pursue dating. Instead, they tended to have levelled and positive views on relationships, seeing them as lifelong commitments focused on companionship (). This suggests a need for providers to expand their awareness of current evidence and deliver evidence-based education.
Training and support were significant issues for many providers. Both parents and teachers reportedly encountered communication challenges when educating adolescents, often needing to repeatedly explain concepts multiple times and adjust their methods due to varying comprehension levels (; ; ). They emphasised the need for ongoing training, support (; ; ; ), and continuous monitoring to improve effectiveness (; ), consistent with previous research (; ). Using a social model of disability can help address these comprehension issues collaboratively (). Similarly, providers also highlighted the need for individualised resources tailored to the needs of adolescents with intellectual disability (; ; ; ; ), consistent with previous research (; ).
Finally, effective education is enabled by increased provider training (; ; ; ), the use of engaging teaching methods (; ; ), active parental involvement (; ; ; ) and collaboration between providers (; ; ), including improved communication and individualised instruction (; ). Parents and teachers should collaborate to provide consistent relationship and consent education at home and school (). Proactive, structured approaches encouraging multidirectional communication and long-term reinforcement through collaborative relationships are essential (; ; ; ; ). Self-determination is often overlooked in sexuality education for individuals with intellectual disability. Only a few teachers focused on autonomy and self-advocacy (; ). There is a gap in linking sexual health with self-determination for adolescents with intellectual disability (). Understanding their sexual self-perceptions and environment can improve relationships and consent education, promoting sexual autonomy and well-being (). There is a need for early investments and positive approaches regarding adolescent sexuality to promote sexual well-being over time (; ; ; ).
This review is unique in addressing the critical need for effective relationships and consent education for adolescents with intellectual disability. It highlights gaps in knowledge and resources and takes a comprehensive approach to investigating the views of both the adolescents and their various care providers regarding relationship and consent education. Given recent changes in consent laws in New South Wales Australia and the mandatory integration of consent education into the national curriculum in Australia and other countries, this study is timely and essential. By increasing awareness about the varied needs and skills of adolescents with intellectual disability, this work aims to shift current paradigms around their sexuality and consent education.
This review assessed the content of education provided in schools, homes, and health, disability care, and support services by various providers, their competencies, and the barriers and enablers for implementing relationships and consent education. The recommendations highlight policy change and implementation support for relationship and consent education that meets the needs of adolescents with intellectual disability. These recommendations include addressing the limited research on adolescents with intellectual disabilities, the need for better access to CSE materials, and the development of tailored educational programs. This review examined the status of sexual and reproductive health rights and consent education among adolescents with intellectual disability and how these rights are upheld in various countries.
Strengths and Limitations of This Review
Our literature review has several limitations. We could only analyse published studies, which varied in sample size and provider groups, making it uncertain how well conclusions apply to all adolescents with intellectual disability. There is a lack of longitudinal data to assess the long-term impact of relationship and consent education. Additionally, the review may be biased towards certain cultural perspectives. Although it included studies from high- and middle-income countries, most were conducted in the USA, making it difficult to generalise findings globally. The heterogeneity of study designs, including qualitative, quantitative, and mixed methods, complicated comparisons. Most studies were qualitative, limiting the ability to quantify the problem. Additionally, few studies reported on healthcare and disability providers’ views, limiting the representation of these perspectives. The review did not assess publication bias or risk of bias.
5. Conclusions
Our review underscores the urgent need for effective relationships and consent education for adolescents with intellectual disability, highlighting significant gaps in knowledge among both adolescents and providers and emphasising the importance of targeted interventions and resources. Adolescents desire comprehensive, evidence-based education, but the quality varies by provider. Many educators and parents feel ill-equipped, leading to inconsistent, risk-focused education. Barriers include cultural attitudes, communication challenges, complex topics, social isolation, lack of training, and limited resources. To improve education, we advocate for tailored resources designed specifically for the education of adolescents with intellectual disability, the use of more engaging methods, increased training, and collaborative approaches between parents and teachers. A shift from risk-based education to promoting sexual well-being and autonomy is essential. We recommend prioritising comprehension and using a social model of disability in education. This includes collaborative curriculum planning, a co-design approach to resource development, and embedding self-determination, autonomy, and self-advocacy skills into a spiral curriculum to enhance personal development and sexual well-being for adolescents with intellectual disability. These recommendations also have broader implications for national education policies and legislation. Policymakers should ensure that comprehensive sexuality education for adolescents with intellectual disabilities is mandated and adequately resourced within national curricula. Legal frameworks should support inclusive education that promotes sexual rights, well-being, and autonomy for all students, with a specific focus on those with intellectual disabilities. Inclusive education incorporates standardised training programs, accessible resources, and frameworks for monitoring and evaluation.
Author Contributions
All authors were involved in the study conceptualisation, design, choice of methodology, software selection and use, data validation, formal analysis and interpretation of findings, data curation, visualisation, writing, revision, editing and project administration. A.D. prepared the original draft. Supervision was provided by I.Z.-M. and F.R. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
All data discussed in this review are available online.
Conflicts of Interest
The authors declare no conflicts of interest.
References
- Algood, C. L., Hong, J. S., Gourdine, R. M., & Williams, A. B. (2011). Maltreatment of children with developmental disabilities: An ecological systems analysis. Children and Youth Services Review, 33(7), 1142–1148. [Google Scholar] [CrossRef]
- American Psychiatric Association. (2022). Diagnostic and statistical manual of mental disorders: Fifth edition, text revision (DSM-5-TR). American Psychiatric Association. [Google Scholar]
- Arksey, H., & O’Malley, L. (2005). Scoping studies: Towards a methodological framework. International Journal of Social Research Methodology, 8(1), 19–32. [Google Scholar] [CrossRef]
- Bosó Pérez, R., Lewis, R., Littlejohn, J., Willis, M., & Mitchell, K. R. (2022). Young people’s sexual wellbeing: A qualitative evidence synthesis protocol. International Journal of Qualitative Methods, 21. [Google Scholar] [CrossRef]
- Brown, M., Linden, M., Marsh, L., Truesdale, M., Sheerin, F., & McCormick, F. (2024). Learning for life, friendships and relationships from the perspective of children and young people with intellectual disabilities: Findings from a UK wide qualitative study. BMC Public Health, 24(1), 2491. [Google Scholar] [CrossRef]
- Brown, M., McCann, E., Truesdale, M., Linden, M., & Marsh, L. (2020). The design, content and delivery of relationship and sexuality education programmes for people with intellectual disabilities: A systematic review of the international evidence. International Journal of Environmental Research and Public Health, 17(20), 7568. [Google Scholar] [CrossRef]
- Colarossi, L., Riquelme, M. O., Collier, K. L., Pérez, S., & Dean, R. (2023). Youth and parent perspectives on sexual health education for people with intellectual disabilities. Sexuality and Disability, 41(3), 619–641. [Google Scholar] [CrossRef]
- DiClemente, R. J., Salazar, L. F., & Crosby, R. A. (2013). Ecological approaches in the new public health. Health behaviour theory for public health: Principles, foundations, and applications. Jones & Bartlett Publishers. [Google Scholar]
- Dupras, A., & Dionne, H. (2014). The concern of parents regarding the sexuality of their child with a mild intellectual disability. Sexologies, 23(4), E79–E83. [Google Scholar] [CrossRef]
- East, L. J., & Orchard, T. R. (2014). Somebody else’s job: Experiences of sex education among health professionals, parents and adolescents with physical disabilities in Southwestern Ontario. Sexuality and Disability, 32(3), 335–350. [Google Scholar] [CrossRef]
- Eyres, R. M., Hunter, W. C., Happel-Parkins, A., Williamson, R. L., & Casey, L. B. (2022). Important conversations: Exploring parental experiences in providing sexuality education for their children with intellectual disabilities. American Journal of Sexuality Education, 17(4), 490–509. [Google Scholar] [CrossRef]
- Family Planning NSW. (2020). Comprehensive sexuality education policy. Family Planning NSW. Available online: https://www.fpnsw.org.au/sites/default/files/assets/CSE-Policy_2020.pdf?form=MG0AV3 (accessed on 24 January 2025).
- Finlay, W. M. L., Rohleder, P., Taylor, N., & Culfear, H. (2015). ’Understanding’ as a practical issue in sexual health education for people with intellectual disabilities: A study using two qualitative methods. Health Psychology, 34(4), 328–338. [Google Scholar] [CrossRef] [PubMed]
- Ford, J. V., Corona Vargas, E., Finotelli, I., Jr., Fortenberry, J. D., Kismödi, E., Philpott, A., Rubio-Aurioles, E., & Coleman, E. (2019). Why pleasure matters: Its global relevance for sexual health, sexual rights and wellbeing. International Journal of Sexual Health, 31(3), 217–230. [Google Scholar] [CrossRef]
- Frank, K., & Sandman, L. (2019). Supporting parents as sexuality educators for individuals with intellectual disability: The development of the home BASE curriculum. Sexuality and Disability, 37(3), 329–337. [Google Scholar] [CrossRef]
- Greene, A., Baugh, M., Sherwood-Laughlin, C., Greathouse, L., Galyan, J., Simic Stanjovic, I., Sangmo, D., Jozkowski, K., Dubie, M., & Chow, A. (2024). Development of a sexual consent intervention for adolescents with intellectual and developmental disabilities. Journal of Applied Research in Intellectual Disabilities, 37(5), e13272. [Google Scholar] [CrossRef]
- Harden, K. P. (2014). A sex-positive framework for research on adolescent sexuality. Perspectives on Psychological Science, 9(5), 455–469. [Google Scholar] [CrossRef] [PubMed]
- Heifetz, M., Lake, J., Weiss, J., Isaacs, B., & Connolly, J. (2020). Dating and romantic relationships of adolescents with intellectual and developmental disabilities. Journal of Adolescence, 79, 39–48. [Google Scholar] [CrossRef] [PubMed]
- Herat, J., Plesons, M., Castle, C., Babb, J., & Chandra-Mouli, V. (2018). The revised international technical guidance on sexuality education—A powerful tool at an important crossroads for sexuality education. Reproductive Health, 15(1), 185. [Google Scholar] [CrossRef]
- Kågesten, A., & van Reeuwijk, M. (2021). Healthy sexuality development in adolescence: Proposing a competency-based framework to inform programmes and research. Sexual and Reproductive Health Matters, 29(1), 104–120. [Google Scholar] [CrossRef]
- Kucuk, S., Platin, N., & Erdem, E. (2017). Increasing awareness of protection from sexual abuse in children with mild intellectual disabilities: An education study. Applied Nursing Research, 38, 153–158. [Google Scholar] [CrossRef] [PubMed]
- Lafferty, A., McConkey, R., & Simpson, A. (2012). Reducing the barriers to relationships and sexuality education for persons with intellectual disabilities. Journal of Intellectual Disabilities, 16(1), 29–43. [Google Scholar] [CrossRef] [PubMed]
- Laganovska, E., & Kviese, E. (2021). Teacher opinions on sexual education of students with intellectual disability in Latvia. In Society. Integration. Education. Proceedings of the international scientific conference (Vol. 3, pp. 119–128). Rezekne Academy of Technologies. [Google Scholar]
- Lindsey, J., & Harding, R. (2021). Capabilities, capacity, and consent: Sexual intimacy in the court of protection. Journal of Law and Society, 48(1), 60–83. [Google Scholar] [CrossRef]
- Löfgren-Mårtenson, L. (2012). “I want to do it right!” A pilot study of Swedish sex education and young people with intellectual disabilities. Sexuality and Disability, 30(2), 209–225. [Google Scholar] [CrossRef]
- Mendes, M. J. G., & Denari, F. E. (2023). Sex and disability: Sexual education of students with intellectual disabilities according to their teachers. Revista Ibero-Americana de Estudos em Educação, 18, e023091. [Google Scholar] [CrossRef]
- Michielsen, K., & Brockschmidt, L. (2021). Barriers to sexuality education for children and young people with disabilities in the WHO European region: A scoping review. Sex Education, 21(6), 674–692. [Google Scholar] [CrossRef]
- Miller, H. L., Pavlik, K. M., Kim, M. A., & Rogers, K. C. (2017). An exploratory study of the knowledge of personal safety skills among children with developmental disabilities and their parents. Journal of Applied Research in Intellectual Disabilities, 30(2), 290–300. [Google Scholar] [CrossRef]
- Mitchell, K. R., Lewis, R., O’Sullivan, L. F., & Fortenberry, J. D. (2021). What is sexual wellbeing and why does it matter for public health? The Lancet Public Health, 6(8), e608–e613. [Google Scholar] [CrossRef] [PubMed]
- Murphy, G. H. (2003). Capacity to consent to sexual relationships in adults with learning disabilities. BMJ Sexual & Reproductive Health, 29(3), 148–149. [Google Scholar] [CrossRef]
- Nelson, B., Odberg Pettersson, K., & Emmelin, M. (2020). Experiences of teaching sexual and reproductive health to students with intellectual disabilities. Sex Education, 20(4), 398–412. [Google Scholar] [CrossRef]
- O’Neill, J., Lima, S., Bowe, K. T., & Newall, F. (2016). The experiences and needs of mothers supporting young adolescents with intellectual disabilities through puberty and emerging sexuality. Research and Practice in Intellectual and Developmental Disabilities, 3(1), 37–47. [Google Scholar] [CrossRef]
- Peters, M. D. J., Godfrey, C. M., Khalil, H., McInerney, P., Parker, D., & Soares, C. B. (2015). Guidance for conducting systematic scoping reviews. International Journal of Evidence-Based Healthcare, 13(3), 141–146. [Google Scholar] [CrossRef] [PubMed]
- Povilaitiene, N., & Radzeviciene, L. (2015). Teachers’ and parents’ attitude to relevance of sexuality education of adolescents with mild intellectual disabilities. Social Welfare: Interdisciplinary Approach, 5(2), 82–90. [Google Scholar]
- Pryde, R., & Jahoda, A. (2018). A qualitative study of mothers’ experiences of supporting the sexual development of their sons with autism and an accompanying intellectual disability. International Journal of Developmental Disabilities, 64(3), 166–174. [Google Scholar] [CrossRef] [PubMed]
- Retznik, L., Wienholz, S., Höltermann, A., Conrad, I., & Riedel-Heller, S. G. (2021). “It tingled as if we had gone through an anthill.” Young people with intellectual disability and their experiences with relationship, sexuality and contraception. Sexuality and Disability, 39(2), 421–438. [Google Scholar] [CrossRef]
- Retznik, L., Wienholz, S., Höltermann, A., Conrad, I., & Riedel-Heller, S. G. (2022). Young people with intellectual disability and their experiences with intimate relationships: A follow-up analysis of parents’ and caregivers’ perspectives. Sexuality and Disability, 40(2), 299–314. [Google Scholar] [CrossRef]
- Rowe, B., & Wright, C. (2017). Sexual knowledge in adolescents with intellectual disabilities: A timely reflection. Journal of Social Inclusion, 8(2), 42–53. [Google Scholar] [CrossRef]
- Schuwirth, L. W., & Van der Vleuten, C. P. (2003). The use of clinical simulations in assessment. Medical Education, 37, 65–71. [Google Scholar]
- Strnadová, I., Danker, J., & Carter, A. (2022a). Scoping review on sex education for high school-aged students with intellectual disability and/or on the autism spectrum: Parents’, teachers’ and students’ perspectives, attitudes and experiences. Sex Education, 22(3), 361–378. [Google Scholar] [CrossRef]
- Strnadová, I., Loblinzk, J., & Danker, J. (2022b). Sex education for students with an intellectual disability: Teachers’ experiences and perspectives. Social Sciences, 11(7), 302. [Google Scholar] [CrossRef]
- Travers, J., & Tincani, M. (2010). Sexuality education for individuals with autism spectrum disorders: Critical issues and decision-making guidelines. Education and Training in Autism and Developmental Disabilities, 45(2), 284–293. [Google Scholar]
- Treacy, A. C., Taylor, S. S., & Abernathy, T. V. (2018). Sexual health education for individuals with disabilities: A call to action. American Journal of Sexuality Education, 13(1), 65–93. [Google Scholar] [CrossRef]
- Tricco, A. C., Lillie, E., Zarin, W., O’Brien, K. K., Colquhoun, H., Levac, D., Moher, D., Peters, M. D. J., Horsley, T., Weeks, L., Hempel, S., Akl, E. A., Chang, C., McGowan, J., Stewart, L., Hartling, L., Aldcroft, A., Wilson, M. G., Garritty, C., … Straus, S. E. (2018). PRISMA extension for scoping reviews (PRISMA-ScR): Checklist and explanation. Annals of Internal Medicine, 169(7), 467–473. [Google Scholar] [CrossRef]
- Tseng, L.-P., Hou, T.-H., Huang, L.-P., & Ou, Y.-K. (2021). Effectiveness of applying clinical simulation scenarios and integrating information technology in medical-surgical nursing and critical nursing courses. BMC Nursing, 20, 229. [Google Scholar]
- United Nations Educational Scientific and Cultural Organisation (UNESCO). (2015). Emerging evidence, lessons and practice in comprehensive sexuality education: A global review. UNESCO. Available online: https://unesdoc.unesco.org/ark:/48223/pf0000243106?form=MG0AV3 (accessed on 24 January 2025).
- United Nations Educational Scientific and Cultural Organisation (UNESCO). (2018). International technical guidance on sexuality education: An evidence informed approach. UNESCO. [Google Scholar] [CrossRef]
- United Nations General Assembly (UNGA). (1979). Convention on the elimination of all forms of discrimination against women (Vol. 20, p. 2006). United Nations. Available online: https://www.bayefsky.com/general/cedaw_c_2006_ii_4.pdf (accessed on 24 January 2025).
- United Nations General Assembly (UNGA). (1989). Convention on the rights of the child (Vol. 1577, pp. 1–23). United Nations. Available online: https://sithi.org/medias/files/projects/sithi/law/Convention%20on%20the%20Rights%20of%20the%20Child.ENG.pdf (accessed on 24 January 2025).
- United Nations General Assembly (UNGA). (2006). Convention on the rights of persons with disabilities (Vol. 61, p. 106). United Nations. Available online: https://static.coorpacademy.com/content/CoorpAcademy/content-OMS/cockpit-who/raw/who_sr_2b3_crpd_v2-1483980517384.pdf (accessed on 24 January 2025).
- Waling, A., Fraser, S., Kerr, L., Bourne, A., & Carman, M. (2019). Young people, sexual literacy and sources of knowledge: A review (ARCSHS Monograph Series No. 119). Australian Research Centre in Sex, Health and Society, La Trobe University. [Google Scholar] [CrossRef]
- Willig, C., & Rogers, W. S. (2017). The SAGE handbook of qualitative research in psychology (2nd ed.). SAGE Reference. Available online: https://www.ocw.upj.ac.id/files/Textbook-PSI-308-Introducing-Qualitative-Research-in-Psychology.pdf?form=MG0AV3 (accessed on 1 October 2024).
- Wolfe, P. S., Wertalik, J. L., Monaco, S. D., & Gardner, S. (2019). Review of curricular features of socio-sexuality curricula for individuals with developmental disabilities. Sexuality and Disability, 37(3), 315–327. [Google Scholar] [CrossRef]
- World Health Organization (WHO). (2006). Accelerating progress towards the attainment of international reproductive health goals: A framework for implementing the WHO Global Reproductive Health Strategy. World Health Organization. Available online: https://iris.who.int/bitstream/handle/10665/69353/WHO_RHR_06.3_eng.pdf?sequence=1&isAllowed=y (accessed on 24 January 2025).
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