Abstract
Objective: Psychological safety (PS) is essential for health and social care professionals (HSCPs) working in high-stress environments. While much of the existing research focuses on PS within teams, less is known about HSCPs’ lived experiences across diverse health and social care settings. This scoping review aims to synthesise the qualitative literature on PS, identifying key barriers and enablers to its development in health and social care workplaces. Methods: A systematic search was conducted across MEDLINE, PsycINFO, Embase, CINAHL, Scopus, Web of Science, and the Cochrane Library, covering a 20-year period (2004–2024). Eligible studies included primary qualitative research exploring HSCPs’ experiences of PS. Screening and data extraction were managed using Rayyan. An inductive thematic synthesis approach was applied to identify key patterns in the data. Results: The review identified several enablers and barriers to PS. The main enablers included (1) feeling safe within the team and (2) personal factors, which encompassed professional skills, experience, social support, and self-care. Conversely, key barriers were identified: (1) the normalisation of traumatic incidents, (2) unsupportive team and management structures, (3) organisational constraints, and (4) a lack of knowledge and training on PS. Conclusions: Understanding the enablers and barriers of PS is critical for improving workplace culture, resilience, and wellbeing among HSCPs. These findings provide a foundation for future research and interventions aimed at strengthening PS at individual, team, and organisational levels across diverse health and social care settings. The results also offer valuable insights for informing policies and practice to ultimately enhance both staff wellbeing and patient care quality.
1. Introduction
Occupations within health and social care services, including nursing, medicine, social work, rehabilitation, welfare work, physiotherapy, occupational therapy, mental health support, and paramedicine, are essential to the functioning of society and often deeply rewarding [1]. These professions provide a sense of purpose, human connection, and the opportunity to make a meaningful difference in the lives of others. However, they are also widely recognised as among the most stressful of all occupations [2,3,4,5,6,7,8]. The combination of high emotional demands, exposure to trauma, heavy workloads, and management of complex patient needs creates a challenging environment that significantly impacts the health and wellbeing of HSCPs.
While HSCPs experience job satisfaction and fulfilment from helping others [9], the associated stress can contribute to serious health risks. The physical consequences of prolonged workplace stress can be severe, including an increased risk of cardiovascular diseases [10,11], musculoskeletal disorders [12], gastrointestinal problems [13], and metabolic disorders [14]. Additionally, HSCPs often report heightened susceptibility to mental health challenges, including burnout, anxiety, depression, chronic fatigue, compassion fatigue, moral injury, post-traumatic stress disorder (PTSD), and suicidal thoughts [15,16,17,18,19,20]. Among all professional occupations, HSCPs have the highest rates of suicide [21], with many facing a constant battle to manage the emotional and psychological toll of their work.
The COVID-19 pandemic has exacerbated these challenges, placing unprecedented stress on HSCPs and increasing the mental and physical burdens of their roles [22]. HSCPs working on the frontlines of COVID-19 care, for instance, faced compounded stress from higher patient loads, exposure to illness, and the emotional burden of witnessing suffering, leading to significant mental health crises among many [16,23]. As a result, there is a growing recognition of the need to understand and address factors that can help mitigate these risks, protect HSCPs’ health, and improve the overall work environment [24].
1.1. The Importance of Psychological Safety at Work
Psychological safety (PS) has emerged as a key factor in fostering a healthier, more effective work environment for HSCPs [25]. PS is foundational in ensuring that professionals feel supported and capable of managing workplace stress without fear of negative consequences. Originally described by Schein and Bennis [26] as an essential element of organisational development, PS was later defined by Kahn [27] as an individual’s sense of being able to express oneself without fear of harming one’s self-image, status, or career. In the context of team dynamics, Edmondson [28] characterised PS as “a shared belief that the team is safe for interpersonal risk-taking”.
PS is particularly important in the context of healthcare and social care settings, for HSCPs operate within a high-stakes environment where collaboration, communication, and trust are essential to providing safe and effective care. The sense of PS encompasses the ability to speak up about patient care issues, share concerns, and seek help when needed without fear of blame or retaliation. Such an environment is crucial for reducing medical errors, improving team collaboration, and ensuring patient safety [29,30,31]. At the same time, PS is vital for the emotional and psychological wellbeing of HSCPs themselves, helping them manage stress, prevent burnout, and foster post-traumatic growth [32,33].
Conversely, when psychological safety is embedded within the workplace culture, it promotes engagement, job satisfaction, and retention—factors that are increasingly important in the face of workforce shortages and high turnover. A workplace that promotes PS not only improves communication and teamwork but also supports HSCPs in navigating the stresses of their roles, thus enhancing both their individual and collective health outcomes [34].
1.2. The Neurophysiology of Psychological Safety
The neurophysiological foundation of PS is also gaining increasing attention, particularly through the lens of polyvagal theory (PVT) [35], which examines how stress impacts the nervous system. PVT explains how individuals respond to stress by activating different autonomic states: ventral vagal (VV), sympathetic activation (SA), and dorsal vagal (DV), which relate to PS [36]. Stressful work conditions, such as those faced by HSCPs, can lead to the activation of the body’s ‘fight or flight’ response (SA) or shutdown response (DV), both of which inhibit optimal functioning and increase vulnerability to burnout [37]. The prolonged exposure to such stress responses leads to an elevated cortisol level, which can cause chronic health issues, including weakened immune function, cardiovascular strain, and even digestive problems [35]. Understanding these neurophysiological mechanisms highlights the importance of fostering PS [38], as a supportive and trauma-informed environment can help regulate these stress responses and contribute to improved mental and physical health [39].
1.3. The Role of Psychological Safety in HSCPs’ Wellbeing
The wellbeing of HSCPs is not only vital for their own health but also for delivering safe, high-quality care to patients [40]. Despite its importance, many HSCPs report a lack of perceived PS in their workplaces, which prevents them from speaking up or addressing concerns, leading to potential errors and heightened stress. Fear of retribution, being ignored, or causing trouble often silences these voices [41]. This culture of silence can contribute to unsafe working conditions, reduce team effectiveness, and increase the likelihood of burnout, moral injury, and turnover among staff. However, research suggests that certain organisational factors can enable PS. These include a positive safety culture, continuous improvement efforts, cohesive team dynamics, ethical leadership, and change-orientated organisational practices [42]. When these elements are in place, HSCPs are more likely to feel safe, supported, and valued, leading to higher levels of engagement and improved job satisfaction, which can significantly improve their mental and physical wellbeing and contribute to safer patient care [43].
2. Focus of the Scoping Review
While much of the existing research on PS has examined its measurement and impact across various occupations [44,45,46], teams [42,43], and at the individual level [9,33,47], there is a growing body of research focused on understanding how HSCPs themselves experience PS in the workplace. This scoping review aims to synthesise the existing qualitative research on the barriers and enablers of PS from the perspective of HSCPs to better understand the factors that influence their ability to feel psychologically safe at work.
3. Objective of the Review
The objective of this scoping review is to identify, collate, and thematically synthesise qualitative research on the factors that enable or act as barriers to PS in health and social care settings. By capturing the lived experiences of HSCPs, the review will inform future interventions and research designed to enhance PS at individual, team, and organisational levels, ultimately improving HSCPs’ wellbeing and the quality of patient care.
4. Research Questions
- Primary Question
What are HSCPs’ experiences of PS within their workplaces?
- Secondary Questions
How is PS conceptualised in the research literature?
- What are the characteristics of participants included in the sources of evidence identified?
- What research designs underpin the literature on PS as experienced by HSCPs?
- What factors are effective in facilitating (enablers) or reducing (barriers) PS among HSCPs?
- What gaps exist in the literature regarding PS as experienced by HSCPs?
5. Method
The purpose of the scoping review method is to map a body of peer-reviewed research literature with the intention to illuminate key characteristics, terms, methods, findings, and relevant gaps to inform future research [48]. The Joanna Briggs Institute (JBI) methodology and checklist for conducting scoping reviews were followed [49]. In terms of reporting style, the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews checklist (PRISMA-ScR) was used [50]. The scoping review adhered to the ENTREQ statement and utilised thematic synthesis [51]. The scoping review protocol was prospectively registered with OSF (https://osf.io/preprints/psyarxiv/4u7hq (accessed on 20 May 2024)) and was published as Hoegh et al. [52].
6. Inclusion Criteria
6.1. Population
The study population included specific mention of ‘health and/or social care professional’ and their experiences of individual or group PS in their work setting. In studies where accounts of HSCPs’ own understandings of PS are included, their own use of terminology (e.g., feeling safe, social engagement) was acknowledged.
Only qualitative studies were included to capture the personal experiences and perspectives of HSCPs’ in terms of PS, as qualitative research enables a deeper exploration of underlying beliefs, concerns, and contextual factors that shape HSCPs’ sense of PS.
6.2. Context
The context was to explore research published worldwide.
6.3. Date of Publication
From March 2000 to February 2024. Databases were searched from 2000, as it was believed that the term “Psychological Safety” became popularised by the work of Edmondson [28] in the late 1990s.
6.4. Types of Evidence
Primary research, qualitative, or mixed methods research which included qualitative data.
6.5. Languages
English only (based on this being the primary language spoken within the context being researched).
7. Exclusion Criteria
Studies that did not include peer-reviewed primary qualitative data, such as quantitative studies, reviews, opinion texts and grey literature, were not sourced. Studies that include qualitative data but do not provide a sufficient proportion for meaningful analysis and inclusion in a thematic synthesis. If a significant proportion of the study population did not focus on HSCPs, then the paper was excluded.
8. Calibration
Prior to commencing the screening process, a calibration exercise was conducted between reviewers [53]. This consisted of selecting 10% of the papers for independent screening by each reviewer. A high level of agreement among reviewers was achieved (higher than 90%) [54,55].
9. Sources of Evidence
Two levels of screening were used to identify sources of evidence for inclusion in the scoping review: (a) study selection—review title and abstract, (b) study screening—review the full text. Data screening, charting and literature quality assessments were managed using Rayyan software (http://rayyan.qcri.org, (accessed on 20 May 2024)) [56] to sift, categorise, sort and store findings according to key issues and themes. Any articles identified as relevant based on the title and abstract were reviewed at the full-text level. A PRISMA flowchart was used to report the final number of the study selection process.
10. Search Strategy
The search strategy for this scoping review was designed to be as comprehensive as possible and developed with the help of an expert health librarian. It was peer-reviewed using the Peer Review of Electronic Search Strategies (PRESS) guidelines [57]. Following the JBI guidelines for conducting a scoping review, a three-step search strategy process was implemented:
- Initial Search: The first step involved performing an initial search of two databases, namely MEDLINE (Ovid) and APA PsycInfo. Text words used in the titles and abstracts of relevant papers identified within this search were extracted and analysed alongside the index terms describing the articles.
- Comprehensive Database Search: These terms were then used in step two, where a further search was conducted across all relevant databases: MEDLINE, APA PsycINFO, Embase, CINAHL, Scopus, Web of Science, and Cochrane Library.
- Reference List Examination: Lastly, step three included examining the reference lists of articles included in the review to identify further relevant sources.
Grey literature was not included in the final review.
The SPIDER (Sample, Phenomenon of Interest, Design, Evaluation, Research type) tool was utilised as the source for the search strategy [58]. This tool was used to define key elements of the review question and search strategy, ensuring a systematic approach to identifying relevant literature (see Table 1).
Table 1.
Search strategy.
11. Data Extraction Process
Data were extracted, duplicates removed, and titles and abstracts were screened. Papers which met the inclusion criteria were retained for full-text screening by four independent reviewers who each screened 50% of the papers. If an abstract did not provide sufficient exclusion information, the article was retained for full-text screening. Two independent reviewers screened full papers using the inclusion and exclusion criteria, and any uncertainty was resolved through discussion. Data extracted from selected studies included author, publication year, title, participant information, context, methodology, results, themes, limitations and type of analysis used. Data are charted using a data extraction table, based on a model recommended by the JBI [59].
12. Risk of Bias
The Critical Appraisal Skills Programme (CASP) checklist for qualitative research is a validated tool for quality assessing qualitative research, and it is endorsed by Cochrane and the World Health Organisation [60]. The checklist is widely used and recommended for novice researchers and is known to be succinct and effective [61]. Furthermore, the checklist was developed for use in health-related research [60]. The CASP checklist tool allows the researchers to systematically evaluate published papers by looking at the reliability, relevance and conclusions drawn. The quality of the included papers was assessed using the tool by four reviewers, with each reviewer assessing 50% of the included studies. Any disagreements were resolved through discussion.
13. Data Synthesis
A thematic synthesis of qualitative data based on the method described by Thomas and Harden [51] was utilised to synthesise and manage the extracted data, and themes emphasising key issues and messages were created. The data synthesis process involved several key steps:
The first step involved line-by-line coding of the primary research. This meticulous process ensured that all relevant data were captured and categorised appropriately. Each line of text from the included studies was examined and assigned a code that summarised its meaning. The initial codes were then re-examined to identify similarities and relationships between them, a process termed “axial coding” [62]. During this stage, the codes were grouped into broader categories, highlighting the connections and patterns within the data. To ensure accuracy and comprehensiveness, the codes were reassessed. This step involved reviewing the codes to ensure they accurately captured the data, a process informed by guidelines from Tricco et al. [63]. This iterative process helped refine the codes and improve the reliability of the coding. Following the reassessment, the codes were organised into logical groups to develop descriptive themes. These themes provided a structured summary of the data, capturing the core messages and issues identified in the primary research. Finally, the reviewers made inferences about the experiences captured by the descriptive themes to generate analytical themes. These analytical themes went beyond mere description, offering deeper insights into the data and providing a more comprehensive understanding of the factors influencing PS among HSCPs. This systematic approach to data synthesis ensured a thorough and robust analysis of the qualitative data, allowing the reviewers to identify key themes and messages related to PS in health and social care settings.
14. Results
Study Characteristics
In total, 11,660 articles were identified. After the removal of duplicates and the screening of titles and abstracts, 630 full-text articles were screened. 48 papers were included in the review. Full details of the search results and the reasons for exclusion are shown in the PRISMA diagram (Figure 1). For full study characteristics, see Table 2. The included studies were published between 2001 and 2023. Sample sizes ranged between 7 and 1636 participants: the total number of participants was 4139.
Figure 1.
PRISMA Flow diagram.
Table 2.
Table of study characteristics.
15. Quality Assessment
The included studies’ methodological quality was judged as being of a high standard overall. However, 37% of the studies did not explicitly state how the risk of researcher bias was minimised or how the relationship between the researcher and the participants had been considered. For further details on the quality assessment, please refer to Table 3.
Table 3.
Quality Assessment.
16. Thematic Synthesis
The aim of this thematic synthesis was to identify, collate and thematically synthesise the qualitative literature to identify the barriers and enablers of PS as experienced by HSCPs across diverse health and social care settings. This section presents findings of the thematic synthesis focusing on the experiences of PS among HSCPs, categorised into positive and negative experiences. Seven analytical themes were derived from the data. Table 4 presents the themes and illustrative quotes. A diagrammatic thematic map (Figure 2) of the enabler and barrier themes identified [111] is also included.
Table 4.
Summary of analytical themes and illustrative quotes.
Figure 2.
Thematic map showing the barriers and enablers of psychological safety identified in the review.
17. Enablers of Psychological Safety
Enablers of PS among HSCPs were identified through two main themes: ‘Personal Factors’ and ‘Feeling Safe Within the Team’.
18. Personal Factors
Personal factors, divided into the subthemes ‘Skills and Experience’ and ‘Social Support and Self-Care’, can promote positive experiences of PS in HSCPs by encouraging speaking up, lowering stress, and increasing confidence in the workplace.
18.1. Skills and Experience
Skills such as emotional intelligence, resilience, and de-escalation were found to enhance psychological safety by equipping HSCPs with the ability to cope with workplace challenges and stress [68]. Additionally, confidence and experience contributed to a sense of security in their roles [81,88,96,99]. Training, adequate resources, and a supportive community were highlighted as crucial for staff wellbeing, fostering a sense of competence and professional growth which was seen as essential for job satisfaction [66,67,75,77,83,94,102,107].
18.2. Social Support and Self-Care
Social support networks, engagement in self-care activities like exercise and meditation, and seeking professional help when needed were identified as promoting PS [69,70,74,79,87,88,96,99,100]. During the COVID-19 pandemic, external support proved essential for coping, underscoring the role of support beyond the workplace [85,91].
19. Feeling Safe Within the Team
Peer support and feeling valued within the team were critical factors in fostering psychological safety [68,86,87,88,96,99,106]. Support from colleagues, both formal and informal, helped alleviate stress and build resilience [72,105]. Positive peer relationships helped to foster a feeling of comradery which helped prevent feelings of isolation [67,70]. Clear communication and a supportive team culture encouraged staff to speak up and share ideas without fear of judgement [87,97,105]. Supervisory support during stressful times further enhanced feelings of safety and support [103,107].
20. Barriers to Psychological Safety
Barriers impacting PS were categorised into four themes: ‘Normalisation of Traumatic Incidents’, ‘Unsupportive Team and Management’, ‘Organisational Factors’, and ‘Lack of Knowledge and Training’.
21. Normalisation of Traumatic Incidents
The normalisation of workplace trauma, violence, and injuries discouraged HSCPs from reporting incidents or admitting mistakes due to fear of judgement or a culture of silence [71,78,82,84,93,95,109,110]. The normalisation of workplace trauma can lead to staff feeling vulnerable and isolated due to fear or lack of support from their organisation [78,83,86,109]. This environment led to psychological distress and physical symptoms of stress among staff, which contributes to burnout [69,79,86,87,90,99,100,109].
22. Unsupportive Team and Management
A negative team culture and hierarchical structures within organisations hindered PS by creating barriers to open communication and support [65,69,82,86,90,93,109]. Lack of management support and poor communication exacerbated stress and dissatisfaction among staff [97,104,105]. Feeling unsafe or scared to speak to management feeds into a perceived lack of support, which affects morale, which impacts feelings of psychological safety [78,93].
23. Organisational Factors
Issues such as understaffing, excessive workload, and inadequate resources contributed significantly to psychological distress and burnout among HSCPs [64,65,69,78,82,84,96,98,101,104]. During the COVID-19 pandemic, insufficient personal protective equipment (PPE) and rapidly changing protocols further exacerbated stress levels and contributed to HSCP feeling concerned for themselves, their colleagues and patients [31,67,70,75,89,91,94,102,107,108].
24. Lack of Knowledge and Training
Lack of training and opportunities for professional development can act as a hindrance for PS, as feelings of inadequacy and lack of growth can contribute to experiencing stress and anxiety and negatively impact job satisfaction [83,92,100]. Insufficient training and knowledge, particularly highlighted during crises like the COVID-19 pandemic, contributed to increased anxiety and uncertainty among HSCPs [31,75,91,94,108]. The lack of preparedness and professional support further diminished PS during such unprecedented events [81].
25. Discussion
This scoping review identifies key factors that influence PS among HSCPs, highlighting both enablers and barriers. Six main factors that affect HSCPs experiences of PS were identified. Factors identified to enable experiences of PS were ‘feeling safe within the team’ and ‘personal factors’ with the subthemes ‘skills and experience’ and ‘social support and self-care’. These enable experiences of PS by increasing confidence and encouraging speaking up and asking for help. The four factors which were identified as contributing towards barriers of psychological safety were: ‘Normalisation of Traumatic Incidents’, ‘Organisational Factors’, ‘Lack of Knowledge and Training’, and ‘Unsupportive Team and Management’.
These findings suggest that interventions aimed at improving PS should focus on enhancing leadership practices, fostering team cohesion, promoting a supportive organisational culture, and providing adequate support systems. Addressing these areas can help create a safer and more supportive environment for HSCPs, ultimately benefiting both professionals and patients. The results also point to significant gaps in the current evidence base, particularly the need for more research on interventions that can effectively enhance PS in diverse healthcare settings. Future research should explore these areas to develop evidence-based strategies that can be widely implemented. By understanding what helps and hinders PS, health and social care organisations can take informed steps to improve the working conditions for HSCPs, contributing to better mental health outcomes, job satisfaction, and patient care quality [9].
This review produced important new information on PS as experienced by HSCPs. It offered insights into the conceptual understandings of PS, characteristics of participants, study design and methodology, and factors that enabled or acted as barriers to PS. Additionally, it highlighted challenges and gaps in the existing evidence base and provided recommendations for key areas for future research and practice. Research is needed to explore the specific factors influencing PS that were under-represented or not addressed in the existing literature. This includes examining the role of organisational culture, leadership styles, trauma-informed practices and team dynamics in fostering or hindering PS [112]. Longitudinal studies could provide deeper insights into the long-term impacts of PS on HSCPs’ mental health, job satisfaction, and patient care outcomes. Such studies could help in understanding how PS evolves over time and the sustained effects of interventions aimed at improving PS [36]. Developing and testing interventions designed to enhance PS in various health and social care settings is crucial. Future research could focus on developing evidence-based strategies and tools to enhance PS and assessing their effectiveness through controlled trials. Additionally, studies should aim to capture psychophysiological data, such as heart rate variability, to gain deeper insights into the physiological correlates of PS [38]. Combining these objective measures with subjective self-reports using validated psychological scales would provide a more comprehensive understanding of HSCPs experiences of PS [33,39].
Expanding research to include diverse health and social care settings and populations will help ensure the findings are more generalisable. Studies should consider different healthcare systems, geographic regions, and socio-cultural contexts to understand how PS varies and what tailored approaches may be needed. Engaging in multidisciplinary research that combines insights from psychology, organisational behaviour, healthcare management, and other relevant fields can provide a more comprehensive understanding of PS. Collaborative efforts can enhance the development of holistic interventions and policies. The findings of this scoping review will help inform the development of impactful resources and build an evidence base on PS in health and social care settings for HSCPs, academics, policymakers, and statutory and third-sector agencies. The aim is to raise awareness and improve research in this area, ultimately leading to developing training programmes for HSCPs and leaders focused on fostering PS, communication skills, and team building; informing policies that prioritise PS in health and social care organisations, ensuring that structures and practices support a safe and supportive working environment; and guiding resource allocation to support initiatives aimed at improving PS, including mental health support services, team development activities, and organisational change efforts. Lastly, the review targets a broad scope of disciplines concerning PS, providing the opportunity to elicit more generalisable findings that can directly inform practice and policy decisions within these disciplines. By addressing the gaps and building upon the findings of this review, future research can contribute significantly to the enhancement of PS, ultimately benefiting both HSCPs and the patients they serve.
26. Limitations of the Review
A key limitation of this scoping review is the exclusion of grey literature due to time constraints and the overwhelming volume of results retrieved through the formal database search strategy. While this decision was necessary to ensure the feasibility and timely completion of the review, it does introduce the potential for publication bias [42,113]. Grey literature often includes valuable research from policy reports, theses, conference proceedings, and government publications, which may contain negative or null findings not found in peer-reviewed journals. As such, our findings may reflect a skewed perspective that over-represents successful interventions or positive outcomes since these are more likely to be published. Additionally, language limitations and access barriers further constrained the evidence base. Only studies published in English were included, which inevitably omits relevant insights from non-English-speaking countries. This is particularly important in a review focused on psychological safety in health and social care, where cultural and systemic differences between countries may significantly influence how PS is understood and experienced. Several potentially eligible studies could not be reviewed in full due to paywall restrictions or access issues, which also means our thematic synthesis is based only on studies we could obtain in full. These limitations may reduce the diversity and inclusivity of our findings and restrict their generalisability to global settings. Future reviews may wish to address these limitations by allowing more time for sourcing grey literature, using translation tools or multilingual review teams, and leveraging open access networks and institutional subscriptions to retrieve a broader range of studies. Doing so would help build a more comprehensive and representative picture of PS across international health and social care contexts.
27. Conclusions
This scoping review details the thematic synthesis of primary qualitative research exploring HSCPs’ perspectives and experiences of PS in their work settings. The review identifies key factors that facilitate or hinder PS and highlights significant gaps in the current evidence base. Recognising what helps and hinders PS in health and social care settings can inform the design and implementation of interventions aimed at fostering environments that enhance PS for both HSCPs and patients in their care. The review produced important new information on PS as experienced by HSCPs, including conceptual understandings of PS, characteristics of participants, study designs, and methodological approaches. It identified factors that enable PS, such as supportive leadership, team cohesion, positive organisational culture, and professional development opportunities. Conversely, barriers such as hierarchical structures, excessive workload, fear of reprisal, and lack of support systems were also highlighted. Significant gaps in the literature were identified, including the need for more intervention studies, research in diverse health and social care settings, longitudinal studies, consideration of socio-cultural contexts, and quantitative measures to complement qualitative findings. Future work and subsequent research could build upon the findings of this scoping review. The review will help inform the development of impactful resources and build an evidence base on PS in health and social care settings for HSCPs, academics, policymakers, and statutory and third-sector agencies. The aim is to raise awareness and improve research in this area, leading to the development of evidence-based strategies that can be widely implemented. By addressing these gaps and focusing on the identified enablers and barriers, health and social care organisations can take informed steps to improve working conditions for HSCPs, contributing to better mental health outcomes, job satisfaction, trauma-informed practices and improved patient care quality. The review will be targeted across a broad scope of disciplines concerning PS, providing the opportunity to elicit more generalisable findings that can directly inform practice and policy decisions within these disciplines.
Author Contributions
Conceptualization, N.P. and N.C.; methodology, J.H., G.R., S.S., A.U. and N.P.; formal analysis, J.H., G.R., S.S., A.U. and N.P.; writing—original draft preparation, N.C. and J.H.; writing—review and editing, N.P.; supervision, N.P. 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
No new data were created or analysed in this study. Data sharing is not applicable to this article.
Public Involvement Statement
No public involvement in any aspect of this research.
Guidelines and Standards Statement
This manuscript was drafted in accordance with the Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews checklist (PRISMA-ScR) for Scoping Review research.
Use of Artificial Intelligence
AI or AI-assisted tools were not used in drafting any aspect of this manuscript.
Conflicts of Interest
The authors declare no conflict of interest.
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