2. Materials and Methods
2.1. Study Design and Setting
This study employed a descriptive cross-sectional design to explore the relationship between self-management behaviors and both clinical and quality-of-life outcomes in adult patients undergoing peritoneal dialysis (PD). The study was conducted at King Saud University-affiliated hospitals in Riyadh, Saudi Arabia, between January and April 2025. Riyadh, the capital and largest city in Saudi Arabia, hosts a variety of tertiary care centers and dialysis units serving a large population of patients with end-stage renal disease (ESRD). The selected sites included nephrology outpatient clinics and home-based peritoneal dialysis programs, offering access to a diverse pool of PD patients receiving routine nursing support. The cross-sectional approach was deemed appropriate to obtain a snapshot of current practices and patient characteristics, providing correlational insights into self-management and outcome variables. The study was conducted and reported following the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) guidelines for cross-sectional studies. A completed STROBE checklist [
26] is provided in
Supplementary Material S1.
2.2. Sample and Sampling Technique
The study population comprised adult patients undergoing peritoneal dialysis (PD) at tertiary and affiliated nephrology centers in Riyadh, Saudi Arabia. Eligible participants were aged 18 years or older, had been receiving PD for at least three months, and were able to provide informed consent. Patients were excluded if they had cognitive or communication impairments that precluded participation, were experiencing acute peritonitis at the time of recruitment, or had a planned modality change (e.g., transition to hemodialysis or transplantation) within 30 days.
A consecutive sampling technique was employed to minimize selection bias and ensure that the sample was representative of the clinic population. All patients who attended routine outpatient PD clinic visits or supply refill appointments during the data collection period (January–June 2024) and met the eligibility criteria were approached for inclusion. Recruitment was conducted by trained research nurses who explained the study objectives, procedures, and confidentiality assurances in a private setting before obtaining written informed consent.
The sample size was determined a priori using G*Power software (Release 3.1.9.7) for multiple linear regression analysis, assuming a medium effect size (f2 = 0.15), α = 0.05, power (1 − β) = 0.80, and six predictors. The required minimum sample size was calculated to be 97 participants. To account for potential non-response and missing data, a 20% margin was added, resulting in a target sample of 120 participants. Ultimately, 165 participants were recruited and included in the analysis, exceeding the required minimum sample size.
2.3. Variables and Instruments
Sociodemographic variables included age (years), sex, educational attainment, marital status, employment status, and monthly household income. Clinical variables comprised dialysis vintage (months on PD), dialysis modality, and comorbidity burden. Comorbidity was assessed using the Charlson Comorbidity Index (CCI), a validated weighted measure that predicts mortality risk based on 19 medical conditions [
27]. Each condition carries a weight from 1 to 6, and scores are summed to yield a total index ranging from 0 to 37, with higher scores indicating greater comorbidity burden [
27,
28]. For descriptive analyses, CCI was reported as mean ± standard deviation and categorized into 0, 1–2, and ≥3 comorbidities.
Self-management behaviors were evaluated across four domains—technical skills, medication adherence, lifestyle modification, and emotional coping—using a structured, validated questionnaire adapted for peritoneal dialysis contexts [
3,
4,
29,
30]. Each domain includes multiple Likert-type items (1–5 scale), and subscale scores are averaged; higher scores indicate greater engagement or coping capacity. The instrument has demonstrated acceptable internal consistency (Cronbach’s α > 0.80) and construct validity in renal populations [
29].
Quality of life was assessed using the Kidney Disease Quality of Life Short Form (KDQOL-36), which combines the SF-12 physical and mental component summaries with three kidney-specific domains (symptoms/problems, effects of kidney disease, burden of kidney disease) [
31,
32]. Each domain is transformed to a 0–100 scale, with higher scores indicating better quality of life. Both total and domain-specific scores were analyzed.
Clinical outcomes included dialysis adequacy (Kt/V), serum albumin, and hospitalization history in the previous 6 months (number and cause of admissions). Laboratory data were extracted from electronic medical records at the time of questionnaire administration.
2.4. Data Collection Procedure
Data were collected over a 12-week period by a team of trained research assistants who had completed a comprehensive orientation on study protocols, questionnaire administration, and ethical procedures. Participants were approached during their PD follow-up visits or contacted through home care services, depending on their treatment arrangement. After verifying eligibility and obtaining informed written consent, participants completed the Arabic versions of the questionnaires in a private setting to ensure confidentiality. For participants with literacy challenges, the research assistant offered to read questions aloud and record responses without influencing answers. Completed forms were reviewed immediately for completeness and any discrepancies clarified with the respondent. Clinical data were extracted from medical records by authorized research staff and recorded under the same anonymized participant ID codes.
2.5. Bias and Confounding
To minimize potential selection bias, we employed a consecutive sampling strategy, inviting all eligible patients who attended the participating peritoneal dialysis (PD) programs during the study period to participate. Standardized data collection protocols were implemented across sites to ensure methodological consistency, and all research personnel received structured training in questionnaire administration and clinical data abstraction. Potential confounders identified a priori—including age, sex, educational attainment, PD vintage, and comorbidity burden (measured by the Charlson Comorbidity Index)—were systematically recorded and included in multivariable models to adjust for their influence on the outcomes of interest. In addition, for analyses involving multiple clinical sites, fixed effects were incorporated to account for potential clustering at the center level. These procedures were designed to strengthen internal validity by reducing both systematic and random sources of bias.
2.6. Missing Data
Patterns and mechanisms of missing data were carefully examined before analysis. The proportion of missingness for each variable was assessed, and Little’s Missing Completely at Random (MCAR) test was performed to evaluate whether data were missing completely at random. For variables with incomplete data, we applied a multiple imputation strategy using predictive mean matching, generating 20 imputed datasets to minimize potential bias and loss of statistical power. The imputation model included key demographic, clinical, and self-management variables to ensure the plausibility of estimates. All primary analyses were performed on the pooled imputed datasets, and sensitivity analyses using complete cases were conducted to assess the robustness of findings. The results of the imputed and complete-case analyses were compared and found to be consistent.
2.7. Statistical Analysis
Data were analyzed using IBM SPSS Statistics (version 26; IBM Corp., Armonk, NY, USA). Continuous variables were summarized as means and standard deviations (SD) or medians and interquartile ranges (IQR), depending on distributional characteristics. Categorical variables were summarized as frequencies and percentages. Group differences were assessed using independent-samples t tests or Mann–Whitney U tests for continuous data, and chi-square or Fisher’s exact tests for categorical data, as appropriate. Correlations between continuous variables were examined using Pearson or Spearman correlation coefficients.
For inferential analyses, we constructed multivariable linear regression models to examine associations between self-management engagement scores (independent variables) and patient-reported quality-of-life domains (dependent variables). Logistic regression models were applied for binary clinical outcomes where applicable. All models reported effect estimates (β coefficients or odds ratios) with 95% confidence intervals (CIs). Model diagnostics included checks for linearity, multicollinearity (variance inflation factor), normality of residuals, and influential observations. Primary outcomes and covariates were prespecified to avoid model overfitting. Analyses presented in Tables 5 and 6 followed a stepwise approach: Model 1 presented unadjusted estimates; Model 2 adjusted for demographic variables; Model 3 further adjusted for educational level and PD vintage; and Model 4 included comorbidity burden (Charlson Comorbidity Index). The level of statistical significance was set at p < 0.05 (two-tailed).
2.8. Ethical Considerations
This study received ethical approval from the Institutional Review Board of King Saud University (Approval No. 25-007, dated 2 December 2024). All procedures adhered to the ethical principles outlined in the Declaration of Helsinki and local regulations governing research involving human participants. Informed consent was obtained from all participants following a detailed explanation of the study’s aims, procedures, benefits, and potential risks. Participation was voluntary, and individuals had the right to withdraw at any time without penalty. Confidentiality was rigorously maintained through anonymization, secure data storage, and restricted access to sensitive information. Before participation, all eligible patients received detailed verbal and written information about the study’s purpose, procedures, voluntary nature, and data confidentiality measures. Written informed consent was obtained from all participants prior to data collection. For participants with limited literacy, the consent form was read aloud in the presence of a witness, and thumbprints were accepted as signatures.
All data were anonymized upon entry into the database. Only de-identified data were used for analysis, and access was restricted to authorized members of the research team.
3. Results
A total of 185 patients were screened for eligibility. Fifteen individuals were excluded prior to eligibility assessment—ten did not meet the inclusion criteria and five declined to participate. Of the 170 eligible patients, seven declined to provide consent, resulting in 163 participants who were enrolled and completed baseline data collection. Subsequently, five participants were excluded from the final analysis due to incomplete questionnaires (n = 3) or missing key clinical data (n = 2). The final analytical sample comprised 158 participants. This flow reflects a high recruitment and retention rate, supporting the representativeness of the analyzed cohort (
Figure 1).
Table 1 presents a detailed profile of the 158 peritoneal dialysis (PD) patients included in this study, offering crucial context for understanding variations in self-management behaviors and clinical outcomes. The sample was slightly skewed toward female participants (57.6%), consistent with regional dialysis population trends in Saudi Arabia, where women often assume caregiving roles and may seek care more proactively. The majority of participants were middle-aged, with nearly three-quarters falling within the 35–64-year age range. This age distribution reflects a population in the productive phase of life, where managing a chronic condition like ESRD can present significant occupational and psychosocial challenges.
Educational attainment varied, with 39.9% having completed secondary education and 36.7% possessing a university-level qualification or higher. These findings are notable given the established correlation between education and health literacy, which may significantly influence a patient’s ability to engage in complex self-care regimens. Nearly half of the participants (46.2%) were unemployed, a factor that could be both a consequence and a contributor to the burdens of dialysis, especially considering the time-intensive nature of PD and its associated fatigue and mobility restrictions. Marital status also appeared significant, with 69.6% being married.
Table 2 provides a comprehensive overview of the clinical and dialysis-related characteristics of the study cohort, highlighting the heterogeneity of disease burden and treatment profiles among patients undergoing peritoneal dialysis. The mean Charlson Comorbidity Index (CCI) score of 1.9 ± 0.7 reflects a moderate level of multimorbidity within this population, consistent with the typical clinical complexity of end-stage renal disease (ESRD) patients. By replacing simple comorbidity counts with the validated CCI, the table offers a more nuanced depiction of patients’ underlying health status, allowing for clearer interpretation in subsequent analyses.
The grouped comorbidity categories (single, double, triple or more) further contextualize this burden, demonstrating that nearly one-third of patients presented with multiple coexisting conditions. This finding underscores the potential challenges these individuals face in managing their treatment regimens and maintaining dialysis adequacy, as well as the need for personalized nursing interventions.
Biochemical indicators, including serum albumin (mean 3.53 g/dL) and hemoglobin (mean 11.2 g/dL), point to variable nutritional and hematologic status within the cohort, which may influence both clinical outcomes and self-management capacity. The average dialysis vintage of 29.7 months indicates that most participants were well established on PD therapy, which may have implications for their adaptation to home-based care and long-term self-management behaviors.
Table 3 displays the descriptive statistics for the four subdomains of self-management among peritoneal dialysis (PD) patients, as well as the total self-management score. The self-management scale used a 5-point Likert format, and internal consistency across all subscales was strong, with Cronbach’s alpha values ranging from 0.79 to 0.88. Among the subscales, technical skills recorded the highest mean score (3.78 ± 0.62), indicating that patients generally felt confident performing the procedural aspects of PD such as exchange techniques and catheter care. Medication adherence followed with a moderate mean score of 3.25 (SD = 0.55), while lifestyle modification was rated lower (mean = 2.94 ± 0.73), suggesting variability in patients’ ability to adapt dietary and activity behaviors to meet dialysis demands. Emotional coping showed the lowest average score (2.71 ± 0.69), reflecting a greater degree of difficulty managing the psychological demands of chronic illness. The total self-management score across the cohort averaged 3.15 (SD = 0.47), with scores ranging from 2.00 to 4.75. These results offer a multidimensional snapshot of patient-reported self-care capacity, highlighting stronger engagement with task-oriented components and relatively lower scores in psychosocial and lifestyle-related domains.
Table 4 presents the mean scores and variability across four domains of health-related quality of life (HRQoL) as measured by the Kidney Disease Quality of Life Short Form (KDQOL-SF) among the 158 peritoneal dialysis patients. The highest average score was observed in the domain of social function (mean = 66.4 ± 11.8), indicating that most participants maintained moderate-to-high levels of social engagement and interpersonal interaction despite the demands of chronic dialysis care. Physical function followed with a mean of 61.8 (SD = 12.3), suggesting a moderate degree of physical capability in performing daily tasks and activities. Emotional well-being demonstrated a slightly lower mean score of 58.7 (SD = 14.1), reflecting a varied emotional adjustment to the chronic illness experience. The lowest score was reported in the domain of disease burden (mean = 52.9 ± 15.7), highlighting the significant impact patients perceived the illness to have on their overall lifestyle, independence, and daily functioning. The wide ranges across all domains (e.g., 25–90 for emotional well-being and 21–78 for disease burden) underscore the heterogeneity in patient experiences, likely influenced by individual coping strategies, social support, and the quality of nursing care received.
Table 5 presents a series of bivariate comparisons examining differences in clinical and quality-of-life outcomes between participants with high versus low self-management (SM) levels. Overall, the findings demonstrate clinically meaningful and statistically significant associations between stronger self-management and several favorable outcomes. Participants in the high-SM group experienced significantly fewer hospital admissions over the preceding six months compared with those in the low-SM group (mean difference = −0.70 admissions, 95% CI −0.91 to −0.49,
p = 0.01), indicating a potential protective effect of better self-management behaviors on acute care utilization. Likewise, serum albumin levels—a key indicator of nutritional and clinical status in dialysis patients—were modestly but significantly higher among those with higher self-management (+0.16 g/dL, 95% CI −0.02 to +0.34,
p = 0.04), suggesting improved clinical stability in this group.
Psychosocial outcomes reflected similar trends. Emotional well-being scores (KDQOL domain) were significantly greater in the high-SM group (+4.80 points, 95% CI +0.53 to +9.07, p = 0.03), consistent with previous literature linking self-efficacy and proactive disease engagement to enhanced psychological adjustment in dialysis populations. Although disease burden scores were lower (indicating better perceived status) among high-SM participants, this difference did not reach statistical significance (−3.90, 95% CI −8.81 to +1.01, p = 0.19). No significant age difference was observed between the groups, implying that these effects are unlikely to be confounded by age distribution (p = 0.36).
Table 6 presents the results of a multivariate linear regression analysis conducted to identify independent predictors of total self-management scores among peritoneal dialysis patients. The model incorporated key demographic, clinical, and psychosocial variables. Educational level emerged as a significant positive predictor (β = 0.208; 95% CI: 0.092 to 0.324;
p = 0.001), indicating that patients with higher education tended to report stronger self-management capabilities. Emotional well-being was also significantly associated with higher self-management scores (β = 0.197; 95% CI: 0.081 to 0.313;
p = 0.001), highlighting the relevance of psychological health in promoting adherence and self-care. In contrast, hospital admissions showed a significant negative association (β = −0.162; 95% CI: −0.271 to −0.053;
p = 0.004), suggesting that frequent hospitalizations may reflect or contribute to diminished self-management capacity. Age and gender did not reach statistical significance in the model (
p = 0.10 and
p = 0.11, respectively), though age exhibited a slight negative trend. The comorbidity index approached significance (
p = 0.06), hinting at a possible inverse relationship with self-management that warrants further exploration.
Table 7 outlines the results of a mediation analysis testing whether emotional well-being mediates the relationship between educational level and self-management score. The total effect of education on self-management was significant (β = 0.273;
p = 0.001), and remained significant even after controlling for emotional well-being (β = 0.211;
p = 0.002), indicating a partial mediation. The indirect effect through emotional well-being was statistically significant (β = 0.062; 95% CI: 0.030–0.110;
p = 0.004), confirming that a portion of the effect of education on self-management is transmitted through its impact on emotional health. These findings suggest that higher educational attainment is associated with better self-management, in part because it contributes to stronger emotional well-being.
4. Discussion
The present study examined the multifaceted dimensions of self-management among patients undergoing peritoneal dialysis (PD) in Riyadh, Saudi Arabia, with a focus on clinical and psychosocial outcomes. The findings underscore the critical role of nursing support in fostering self-management behaviors and improving both physiological and quality-of-life parameters in PD populations. Our results affirm and extend existing literature by highlighting the strong association between emotional well-being, educational attainment, and self-care efficacy, offering implications for integrated nursing strategies.
Participants in this study demonstrated relatively high proficiency in technical PD skills, aligning with prior research indicating that patients often master procedural components after adequate nursing instruction and repetition [
33,
34]. However, lower scores in lifestyle modification and emotional coping reflect a known gap in self-management competency, consistent with findings from international studies suggesting that behavioral and affective domains are often underserved in dialysis education [
35,
36,
37]. This imbalance may partially result from conventional training programs’ emphasis on mechanical procedures rather than holistic adaptation to chronic illness [
38,
39].
The significant associations between self-management scores and clinical outcomes—such as hospital admission frequency and serum albumin levels—further validate the clinical utility of promoting self-care behaviors in PD. Previous research supports the protective effect of self-management on infection rates, nutritional status, and hospitalization risk in dialysis patients [
40]. Notably, our data indicate that patients with higher self-management engagement exhibited better emotional well-being, echoing studies that conceptualize self-efficacy as both an outcome and determinant of psychological adjustment in chronic illness [
41,
42]. This bidirectional relationship highlights the need for psychosocial support as an essential component of self-management interventions.
Consistent with earlier work, we identified educational level as a key predictor of self-management capacity [
43,
44,
45]. Health literacy, which often correlates with formal education, plays a central role in determining patients’ understanding of treatment instructions, symptom interpretation, and medication adherence [
46]. Interventions that address literacy gaps through visual aids, simplified materials, and interactive coaching have shown promise in improving self-management and should be embedded into nursing protocols [
47,
48]. Given the cultural context of the current study, incorporating Arabic-translated tools and culturally sensitive education materials likely contributed to patients’ receptiveness and comprehension.
Emotional well-being was found to mediate the relationship between educational level and self-management, underscoring the psychological underpinnings of effective chronic disease management. Emotional distress has been linked to decreased motivation, cognitive impairment, and avoidance behaviours, all of which can undermine dialysis adherence [
49]. Psychological interventions, such as cognitive-behavioral therapy, mindfulness, and motivational interviewing, have demonstrated efficacy in enhancing treatment engagement in ESRD populations [
50,
51]. Nurses trained in basic psychosocial screening and communication techniques can play a pivotal role in identifying at-risk patients and initiating early interventions [
52,
53].
While disease burden was perceived as moderate across the sample, its lack of significant differentiation between self-management groups may reflect the complex interplay between subjective appraisal and objective disease metrics. Patients may adjust their perception of burden over time through cognitive reframing or normalization, phenomena observed in qualitative accounts of dialysis adaptation [
54]. This highlights the importance of combining subjective and objective indicators when assessing treatment outcomes.
Culturally, this study adds to the limited literature on PD self-management in Middle Eastern contexts. In Saudi Arabia, familial involvement, religious beliefs, and hierarchical patient-provider dynamics may influence patient autonomy and emotional coping strategies [
55]. Prior research has suggested that leveraging family engagement in care plans can enhance adherence and reduce psychological distress in chronic disease populations [
56]. Accordingly, culturally informed nursing interventions that incorporate family education and spiritual sensitivity may yield greater impact in the region.
The integration of technology into PD self-management support, although not the focus of this study, represents a promising adjunct to traditional nursing strategies. Telehealth, mobile apps, and home-monitoring tools have shown effectiveness in enhancing patient education, adherence tracking, and remote symptom management [
57]. Future research may explore how digital platforms can augment nurse-delivered self-management support, particularly for patients in remote or underserved areas.
4.1. Implications for Clinical Practice
The findings of this study carry several important implications for clinical practice in peritoneal dialysis (PD) care. First, the observed associations between higher self-management levels and better clinical (fewer hospital admissions, higher serum albumin) and psychosocial (greater emotional well-being) outcomes underscore the central role of nurses in fostering patients’ self-management capacities. Structured nurse-led education, reinforcement of skills, and emotional support should not be viewed as adjuncts but as core clinical activities that directly affect outcomes. Recent evidence highlights that structured self-management interventions—particularly those combining motivational interviewing, individualized education, and telehealth follow-up—can improve clinical stability, reduce hospitalization risk, and enhance patient engagement in home dialysis programs [
58].
Second, the strong link between emotional well-being and self-management suggests that psychosocial support should be systematically integrated into PD programs. Nurses are well positioned to deliver relational interventions, such as empathic communication and shared decision-making, which have been shown to improve patients’ emotional adjustment and self-care behaviors [
59,
60]. Embedding brief psychosocial assessments and targeted counseling into routine PD visits can help identify patients struggling with emotional coping, allowing timely intervention before clinical deterioration occurs.
Third, the results reinforce the value of multidimensional, personalized education strategies. Tailoring content to patients’ health literacy levels, cultural context, and preferred learning styles increases self-efficacy and facilitates behavior change [
6,
7,
8]. Integrating digital platforms (e.g., mobile apps, tele-education modules) with traditional nurse-led teaching may enhance knowledge retention and enable more frequent, flexible follow-up, particularly for geographically dispersed populations [
61].
Finally, at the service-delivery level, PD programs should consider formalizing self-management support as a quality indicator, aligning with international initiatives advocating patient empowerment and shared care models in home dialysis [
62]. This may involve incorporating standardized self-management assessment tools into electronic health records, setting programmatic targets for nurse-patient education encounters, and supporting ongoing staff training in relational and motivational communication skills.
4.2. Implications for Nursing Practice
The findings of this study offer compelling evidence for the transformation of nursing practice in the context of peritoneal dialysis (PD) through personalized, holistic self-management support. First, nurses should move beyond the traditional task-oriented model and adopt multidimensional patient education strategies that integrate psychosocial components, particularly emotional coping and motivation building, into routine care. Second, the strong predictive role of educational level and emotional well-being suggests the need for health literacy screening tools and emotional health check-ins to be embedded within PD nursing assessments. Third, nurses can leverage technology-assisted education, such as Arabic-language mobile apps or interactive videos, to bridge literacy gaps and promote consistent engagement with self-management protocols. Moreover, nurses should actively collaborate with families in culturally appropriate ways, acknowledging their role as co-facilitators of care in collectivist societies like Saudi Arabia. Finally, the demonstrated link between fewer hospitalizations and higher self-management points to a need for community-based nurse navigator programs, specialized roles where nurses conduct home visits or teleconsultations to proactively address challenges and reduce avoidable admissions. These findings reinforce the necessity of positioning nurses as central agents of behavioral change, psychosocial support, and advocacy within the home dialysis continuum.
4.3. Limitations of the Study
This study has several limitations that should be acknowledged. First, its cross-sectional design precludes any causal inference between self-management and the observed clinical or psychosocial outcomes. While statistically significant associations were identified, the temporal direction of these relationships cannot be established. Second, despite careful adjustment for key covariates, potential residual confounding remains a concern. Unmeasured factors such as health literacy, social support, and provider-level variations in care may have influenced both self-management behaviors and outcomes.
Third, selection bias is possible because recruitment occurred within a single regional dialysis network, and participation required patients to attend scheduled clinical visits. Consequently, individuals with lower engagement or access barriers may be underrepresented, which could bias the observed associations toward more favorable outcomes. Fourth, the study relied on self-report instruments for several key constructs (e.g., emotional well-being, self-management behaviors), which are subject to recall and social desirability biases.
Fifth, the constructs of emotional coping and emotional well-being show conceptual overlap, raising the possibility of inflated associations due to shared measurement variance. Future studies could address this by employing factor analysis or using distinct measurement tools to disentangle these related domains. Finally, because data were collected from a single geographic region in Saudi Arabia, the generalizability of the findings to other dialysis populations or healthcare systems may be limited. Replication in larger, multicenter cohorts and prospective designs would strengthen the external validity and causal interpretation of these findings.