1Faculty of Nursing, Universitas Indonesia, Jawa Barat 16424, Indonesia
2Department of Nursing, Poltekkes Kemenkes Jakarta I, Daerah Khusus Ibukota Jakarta 12450, Indonesia
3Faculty of Medicine, Universitas Indonesia, Daerah Khusus Ibukota Jakarta 10430, Indonesia
4Faculty of Public Health, Universitas Indonesia, Jawa Barat 12345, Indonesia
5Department of Nursing, Poltekkes Kemenkes Palembang, Sumatera Selatan 30135, Indonesia
6Nursing Department, Universitas Muhammadiyah Kudus, Jawa Tengah 59316, Indonesia
*Corresponding Author’s Email: ratna_aryani@poltekkesjakarta1.ac.id
ABSTRACT
Keywords: Colorectal Cancer; Patient Care; Self-Management; Systematic Review
Colorectal cancer (CRC) is the third most prevalent cancer globally, accounting for about 10% of all cancer diagnoses and ranking as the second leading cause of cancer-related deaths (World Health Organisation (WHO), 2023; Bray et al., 2024). By 2040, CRC cases are expected to rise to 3.2 million, with 1.6 million deaths (Sung et al., 2021). Both developed and developing countries, especially those with low and middle economic levels, are experiencing increasing CRC incidence rates, impacting patient health and QoL levels (Arnold et al., 2017; Khan & Lengyel, 2023; Alessy et al., 2024). High-incidence countries have reduced CRC rates through healthier lifestyles and improved screening, but globally, the burden remains high, particularly where access to interventions is limited (Bray et al., 2024; Zhou et al., 2024). Early screening is crucial, as CRC is often asymptomatic in early stages (Liu, Ye & Jia, 2024); American Cancer Society, 2021). Despite treatment advancements, patients continue to face symptoms and the side effects, such as rectal bleeding, bowel changes, weight loss, neuropathy and psychological distress, that impair QoL (Han, Yang & Syrjala, 2020; Gosselin et al., 2016; Vlaski et al., 2024).
Recognising these challenges, holistic care approaches like nursing led self-management interventions are essential. Effective self-management empowers patients to handle symptoms and lifestyle changes (Barlow et al., 2002; Lorig & Holman, 2003; Aryani, et al., 2024a). However, many interventions lack personalisation and integration into nursing practice, and inconsistent research makes it difficult to identify best practices (Husebø, Karlsen & Husebø, 2020; Aryani et al., 2024b; Aryani et al., 2023). Barriers to self-management persist, requiring tailored strategies and innovative approaches, such as digital health solutions, to improve engagement and outcomes. Despite growing literature, no recent systematic review has comprehensively mapped and critically appraised the range of self-management interventions for CRC patients, particularly considering new digital personalised approaches. This review uniquely integrates traditional and technology-enhanced strategies, focusing on effective components for diverse patient groups. By synthesising current evidence, we aim to propose a conceptual framework to guide tailored, patient-centred nursing interventions. This systematic review aims to bridge the gap by (1) identifying self-management approaches for CRC patients and (2) evaluating their effectiveness. By highlighting key strategies, we seek to provide evidence-based recommendations for healthcare providers and policymakers.
This systematic review followed the Cochrane Handbook (Higgins et al., 2024) and PRISMA guidelines (Page et al., 2021).
Search Methods
A comprehensive search was conducted across nine databases (JSTOR, Emerald Insight, Oxford Academic, ScienceDirect, SAGE, Clinical Key, ProQuest, Scopus, and Taylor & Francis) using keywords related to "colorectal cancer" OR "colorectal survivor" OR “bowel cancer" OR "colorectal tumour" OR "colorectal neoplasm"; "self-management programme" OR "self- management training", OR "self-management intervention"; and "randomised controlled trial" OR "experimental study". Titles and abstracts were screened using content analysis to identify relevant articles.
Studies were included if they: (1) involved adults (>18 years) undergoing primary CRC therapy,(2) used self-management intervention, (3) were RCTs published in peer-reviewed, open-access journals from January 2013-February 2022, (4) were in English, and (5) provided full text. Excluded were encyclopaedia, book chapters, conferences, correspondence, editorials, news, practice guidelines, protocols, systematic reviews, literature reviews, and articles involving children, newly diagnosed patients without primary intervention, or those not completing primary therapy.
Data extraction was conducted to ensure accuracy and relevance. The first author (AR) conducted screened articles, excluding those clearly outside the inclusion criteria. Articles of uncertain relevance underwent full-text review. Figure 1 (PRISMA flow chart) illustrates the process. An electronic search identified 668 articles, with two excluded before screening. Title and abstract review excluded 449, leaving 217 articles for full-text assessment based on publication year, type, open-access status, and English language.
Nine articles met the final inclusion criteria; 208 were excluded for reasons such as not involving CRC patients, being protocol/development studies, lacking clinical trials/interventions, not following Population, Intervention, Comparison, and Outcome (PICO), not reporting intervention/control group results, or being reviews, conference papers, posters, abstracts, or lacking full texts. Of these, eight did not involve CRC patients, and five did not follow PICO. Ultimately, nine articles were included and are summarised in the following table.
Risk of bias was assessed by using JBI's (Joanna Briggs Institute) critical appraisal tools with 13 criteria rated as "yes," "no," "unclear" (UC), or "not mentioned" (NA). Table 1 summarizes the adherence to criteria across various studies. Zhang et al. (2014) met 12 out of 13 criteria, while four studies (Mayer et al., 2018; Willems et al., 2017; Giesler et al., 2017; Raphaelis et al., 2020) met 11 criteria. Two studies (Knoerl et al., 2019; Takano et al., 2021; Reiter et al., 2021) met 9 criteria, and Yaacob et al. (2020) met 8 criteria, primarily due to missing details on blinding and randomization. Overall, the studies exhibited a low to moderate risk of bias, indicating a need for more consistent and transparent reporting practices.
Assessed Items | Zhang et al. (2014) | Mayer et al. (2018) | Knoerl et al. (2019) | Takano et al. (2021) | Willems et al. (2017) | Giesler et al. (2017) | Raphaelis et al. (2020) | Reiter et al., (2021) | Yaacob et al., (2020) |
Randomisation for sample selection was done correctly. | Yes | Yes | UC | Yes | Yes | Yes | Yes | Yes | No |
The assignment to the intervention group was hidden. | NA | NA | NA | UC | Yes | Yes | Yes | NA | NA |
The intervention group had similar characteristics to the control group. | Yes | Yes | Yes | UC | Yes | Yes | Yes | Yes | Yes |
Respondents were blinded to a group assignment. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
A person delivering the intervention was blinded to group assignment. | Yes | Yes | NA | NA | NA | NA | NA | NA | NA |
Outcome assessors were blinded to a group assignment. | Yes | UC | NA | NA | NA | NA | NA | NA | NA |
Intervention and control groups received the same treatment (other than the intervention). | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Follow-up is complete. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Participants were analysed in the group to which they were randomized. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Outcomes of the intervention group were measured using the same method as that for outcomes of the intervention group. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Outcomes were measured using a reliable method. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
The statistical analysis used was appropriate. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
The trial design was appropriate for the topic, and there were differences between methods and analysis from standard RCTs. | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes | Yes |
Total number of criteria | 12/13 | 11/12 | 9/13 | 9/13 | 11/13 | 11/13 | 11/13 | 10/13 | 9/13 |
The researchers obtained ethical clearance from the Institutional Review Board at Muhammadiyah Institute of Technology and Health, Indonesia with reference number 13/II.I.AU/KET.ETIK/II/2025, on 13th February 2025.
The systematic review identified nine RCT articles that provide valuable insights into self- management interventions for CRC patients (table 2). Publication years ranged from 2014 to 2021, with studies conducted in Asia (3), America (2), and Europe (4). Sample sizes varied from 75 to 462, across cancer centres, clinics, and hospitals. Two studies only specified the country (Mayer et al., 2018; Giesler et al., 2017), highlighting the global relevance of these interventions.
No | Researchers, Years, Respondents & Country | Duration, Time of Measurement, & Interventions Performed | Results & Limitations |
1 | Zhang et al. (2014) N=121 (CG =53, IG=68) China | Six months Baseline, month three, month six IG: received standard care plus a six- month psycho-educational self-efficacy programme, including: One-on-one education from an oncology nurse (one hour) before discharge, post- surgery, and at chemotherapy initiation. A pocketbook covering chemotherapy effects, exercise, nutrition, self-efficacy improvement, and common CRC issues. 30 minutes audio relaxation techniques (breathing and muscle relaxation) to reduce stress and chemotherapy effects, used 12-24 hours before chemotherapy or as needed. Health-coaching phone follow-ups by oncology nurses, 4 times monthly (20-40 minutes each), tailored to individual needs. CG: received standard care and routine nurse instruction (about 30 minutes) before treatment on chemotherapy and its side effects. Additional information was available from doctor or nurse as needed or during follow-up visits. | Results Repeated measures MANOVA showed the IG had significantly greater improvements in self-efficacy (F=7.26, p=0.003) and reductions in severity (F=5.30, p=0.01), symptom distress (F=4.06, p=0.025), anxiety (F=6.04, p=0.006), and depression (F=6.96, p=0.003) at the 3 and 6 months compared CG. No significant differences were found in perceived QoL. Limitations Conducted in only 2 hospitals and 1 cancer centre in Southern China, limiting generalizability; studies in others Asian region are needed. The 6-month follow-up is short for cancer, restricting assessment of long-term effects. |
2 | Mayer et al. (2018) N=284 (CG=140, IG=144) USA | Six months Baseline, month three, month six, month nine IG: Both groups received identical treatment, but the IG used Survivor CHESS smartphone app for information, support, and health promotion, requiring 150 hours of access per week. After 6 months, a licensed trainer coached participant on physical activity through conversation, group or individual sessions, and private messages to encourage engagement. CG: Patients received: The National Cancer Institute's Facing Forward: Life after Cancer Treatment booklet The cancer survival toolbox from the National Coalition for Cancer Survivorships. A pedometer to track steps. | Limitations The study depended on rapid technological advances and growing technology adoption. Possible bias towards respondents comfortable with technology. Sample was not representative: 89% Caucasians, 46% highly educated, and 97% insured, unlike the general U.S. population. Reliable service delivery was identified across diverse geographic areas. |
3 | Knoerl et al. (2019) | Nine weeks | Results |
N=370 (CG=188, IG=182) USA | Baseline, third, sixth, and ninth week IG: was given the Electronic Symptom Assessment and Self-Care (ESRA-C), which includes tools for tracking, education, communication coaching, symptom control, and self-reporting. CG: Standard tools (electronic symptom assessment, participant symptom reports). | Most responders (73.8%) followed the advice of their clinicians. Only a small percentage of respondents (49.2%) employed additional self- management techniques for SQIs. Limitations Not mentioned | |
4 | Takano et al. (2021) Jepang N=200 (CG=100, IG=100) Japan . | 24 weeks (six months) Baseline, week 12, week 24 IG: Patients received standard chemotherapy, supportive care, and a Japanese self-help workbook with: Information on the disease, care, coping, medical information, communication with healthcare providers, decision-making, and goal setting. A questionnaire to identify goals, priorities, and questions for medical staff. Periodic surveys and review of recommendations at week 12 and 24 to assess engagement and behaviours. CG: Patients received standard chemotherapy and supportive care only, without a workbook. | Results GQOL scores at baseline, week 12, and week 24 were as follows: CG: 63.4 (22.0), 60.3 (23.4), and 60.8 (21.5) IG: 65.9 (19.8), 63.5 (20.5), and 63.1 (19.6) No significant interaction between intervention and time points (P=0.964), nor on functional scales. Limitations The workbook was used without direct expert support. Few subgroups and unbalanced baseline characteristics (age, metastasis, prior chemotherapy). Single-study with a uniform population (breast, colorectal, stomach, and lung cancers with or without metastases). |
5 | Willems et al. (2017) N=462 (CG=231, IG=231) Netherlands | 12 months baseline in month 3, month 6, and month 12 IG: For 6 months, patients accessed the eHealth KNW platform anytime, choosing from 8 video modules on topics such as work, fatigue, anxiety, depression, relationships, social life, physical activity, smoking cessation, and nutrition. Modules, based on Cognitive Behavioural Therapy (CBT) and Problem-Solving Therapy (PST), could be completed in any order. PST: 2 sessions with 4 components: identification, goal setting, psychoeducation, action plans, and a 30- days follow-up for goal review. CBT: Included psychoeducation, relaxation, and assignments like behavioural tracking, recognizing | Results No differences were observed in emotional / social functioning, depression, or exhaustion between IG and CG at 12 months. Moderator analyses showed that at 6 months, the intervention reduced depression in chemotherapy patients (d=0.36), fatigue in those ≤56 years (d=0.44), and improved social functioning in men (d=0.34). At 12 months, social functioning was higher in those with secondary education (d=0.19) and lower in those with less education (d=0.22). Limitations |
dysfunctional thoughts, planning enjoyable activities, and setting new goals. CG: received usual care. | Drop-out rates, especially in IG, may have influenced results, though they were low at 6 and 12 months (11.5%, 17.5%). The sample included many women with breast cancer, who generally had high QoL and low depression. | ||
6 | Giesler et al. (2017) N=212 (CG=109, IG=103) Germany | 6 weeks Baseline, week 2, week 6 IG: had access to the website for two consecutive weeks. CG: did not receive treatment until after six weeks. | Results Participants averaged 54 years old (SD 11.1), 58.8% were female, and 73.6% had prior exposure to others’ patient experiences online, making the CRC website module ineffective. No intervention effect was observed at 2- or 6- weeks post-baseline. Limitations Respondents were younger (mean=54.1) than the typical German CRC patient (mean=71). Smaller sample size reduced statistical power; extending recruitment was not possible due to time and website launch constraints. |
7 | Raphaelis et al. (2020) N = 153 (CG=92, IG= 61) Austria | 24 days Baseline, week 2, week 4, and week 8 after hospital discharge using a mailed or online questionnaire. IG: Nurses with at least 2 years of cancer care experience delivered structured pain self-management (Antipain) after completing 19 training sessions (average duration: 1 hour 36 minutes). CG: received standard care. | Results Session averaged 33 minutes in person (usually 2 meetings) and 17 minutes by phone. Only 46% the 9 wards implemented the intervention, with adjustments for power outages. Sub-analysis showed a significant pain reduction (p=0.009) in these wards, though no overall effect was found. Secondary outcomes showed improvements in in- hospital pain treatment (p=0.018), satisfaction with pain self-management information (p=0.002), and self-efficacy (p=0.033). Limitations Recruitment was slower and varied across wards and hospitals. |
8 | Reiter et al. (2021) | The study's timeline and measurement intervals were unspecified, but as a quasi- | Results |
N = 75 (CG=75, IG= 189) Germany | experimental pilot, the duration was likely short, focusing on feasibility and impact. IG: received structured oncology nurse and nutritional counselling (inpatient and outpatient). CG: received standard care. | The intervention group benefited from inpatient nurse counselling for discharge management. No differences were noted in general or gastrointestinal side effects, except for xerostomia and dysphagia. However, 90% of those receiving both inpatient and outpatient counselling managed side effects better. Structured nutritional counselling increased receipt of nutritional information (p=0.001), improved identification of food intolerances (p=0.023), and greater adherence to dietary advice (p=0.003). Most in this group had improved gastrointestinal side effects, except for 4 cases of weight loss. Limitations Small sample sizes, short follow-up periods, and potential bias in patient- reported outcomes. Further research is needed to develop comprehensive, sustainable support systems for cancer patients. | |
9 | Yaacob et al. (2020) N=100 (CG=50, IG=50). Malaysia | 2 weeks Baseline, week 2 IG: used the ColorApp for two weeks CG: did not have access to the app. | Results The IG had a greater increase in knowledge scores after using the ColorApp compared to the CG. No significant change in attitudes towards CRC screening in either group. The app improved knowledge, but attitudes change may need longer exposure and additional strategies. Limitations Attitude change likely requires longer and more comprehensive interventions. |
Three articles included only CRC patients with specific criteria (diagnosed for at least six months, stages I-III, or diagnosed three years prior (Zhang et al., 2014; Mayer et al., 2018; Giesler et al., 2017), while the other six included CRC alongside other cancer types. Intervention duration ranged from 24 days to 12 months and reflected differences in patient needs, cancer stage, and targeted outcomes. Shorter interventions (Raphaelis et al., 2020) focused on acute symptom management, while longer ones (Willems et al., 2017) aimed at sustained behaviour change and long-term QoL. Methods included psychoeducation, smartphone apps, self-help workbooks, eHealth, pain self-management, oncology and nutritional counselling, and health education apps. Control groups received either the same intervention or standard care post-study. These varied approaches underscore the adaptability and multifaceted nature of self-management strategies.
Most interventions yielded positive outcomes, including improvements in self-efficacy, QoL, distress, anxiety, depression, physical activities, adherence, symptom management, functioning, competence, social support, and pain management. Notably, Zhang et al., (2014) reported significant increases in self-efficacy and reduction in symptom severity and psychological distress. Mayer et al., (2018) found improved physical activity at 6 months, though not sustained at 9 months. Knoerl et al., (2019) noted high adherence, no significant compliance. Takano et al., (2021) showed emotional functioning benefits from self-help workbooks. Willems et al., (2017) found subgroup-specific improvements. Raphaelis et al. (2020) reported better pain management and self-efficacy. Reiter et al., (2021) observed improved management of side effects and nutritional challenges. Yaacob et al., (2020) found increased knowledge but no significant attitude change, suggesting longer exposure may be needed. Overall, these findings support the effectiveness of self-management interventions for CRC patients.
The findings from this systematic review highlight the critical role of self-management interventions in CRC care. Programmes like Coping-Together demonstrate benefits for patient- caregiver dyads, showing the value of both lay and clinician guidance (Wiesenfeld et al., 2025; Lambert et al., 2025). Integrating these interventions into standard care can be achieved with personalised electronic care planning tools, such as the COMPASS-CP for CRC survivors (Sohl et al., 2023). Aryani et al., (2024b) identify innovative strategies, including psychoeducational programmes, technology-based interventions, and structured counselling that collectively enhance patients' self-management and QoL. Despite the promising outcomes, several challenges remain. A major gap is the limited understanding of barriers and enablers in cancer self-managing, such as lack of awareness limited access, and emotional hurdles (Pallin et al., 2024). Addressing these barriers is crucial for maximising intervention effectiveness.
The review emphasises the need for interventions that address both physical and psychosocial aspects, including soft skills like self-efficacy and acceptance. Higher self-efficacy improves symptom control and reduces anxiety and depression (Zhang et al., 2014; Mayer et al., 2018). Good self-acceptance aids adaptation, reduces stigma, and enhance social relationships. Current interventions often overlook these aspects, highlighting a gap for more uniform approaches for comparison. Innovative approaches and technologies are essential for comprehensive, patient- centred care. Nurses play a pivotal role in designing, implementing, and evaluating self- management interventions, bridging clinical guidelines and patient needs. By applying evidence- based practices, nurses tailor interventions, improving adherence and QoL (Kitsiou et al., 2025).
Lambert et al. (2025) emphasise nurses' role in translating evidence-based interventions through a stepped-care approach, enhancing self-efficacy and empowerment. Ejezie et al. (2025) highlight digital health interventions where nurses boost engagement and adherence by providing timely support and education. Nurses integrate self-management interventions to enhance outcomes, as shown by Jarelnape et al. (2024), who demonstrate significant improvements due to direct interactions and personalised care. Nurses educate patients, equipping them to manage conditions, adhere to treatments, identify risks, and prevent adverse events. Sassen (2023) underscores nurses' critical role in promoting health. The nurse integration model includes cognitive-behavioural therapy, online learning, and support groups (Aryani et al., 2023). Oncology nurses provide essential skills for managing symptoms, psychological adjustment, and relaxation, crucial for cancer recovery and QoL (Wang et al., 2023). In summary, nurses are essential in shaping CRC self-management, integrating clinical knowledge with patient-centred care to improve outcomes.
Further research should explore interventions that improve soft skills, such as acceptance and self-efficacy, within self-management programmes. Longitudinal studies are needed to assess the long-term effects of these skills on CRC patients' QoL. However, this systematic review is limited by the small number of articles on CRC interventions, which may restrict generalisability. Additionally, the heterogeneity of interventions and methodologies across studies complicates direct comparisons and synthesis of results. Most studies included homogeneous populations, further limiting the applicability of findings to broader patient’s groups. Short follow-up periods in many studies also hinder the assessment of long-term intervention effects and sustainability. Enhancing soft skills, particularly acceptance and self-efficacy, is crucial for improving QoL. Future studies should include more diverse populations, longer follow-up periods and standardised protocols to facilitate effective comparisons and strengthen evidence for CRC self- management strategies.
This systematic review is subject to several limitations. Firstly, the number of eligible studies was relatively small, with only nine randomised controlled trials meeting the inclusion criteria. This restricts the generalisability of the findings, especially given the diversity of interventions, sample characteristics, and settings. Secondly, considerable heterogeneity existed among the included studies in terms of intervention duration, delivery methods, outcome measures, and populations involved, making it challenging to perform a meta-analysis or direct comparison of effectiveness. Thirdly, many studies lacked long-term follow-up, limiting the ability to evaluate the sustained impact of self-management interventions on colorectal cancer patients’ quality of life and psychological well-being. Additionally, several studies focused on mixed cancer populations rather than colorectal cancer patients exclusively, which may dilute the relevance of the findings to this specific group. Moreover, the risk of bias assessments revealed inconsistencies in reporting randomisation procedures, blinding, and intervention fidelity, suggesting that some findings may be influenced by methodological weaknesses. Lastly, most studies were conducted in high-income countries, with limited representation from low- and middle-income settings, thereby reducing the global applicability of the results.
These findings highlight the crucial role of self-management strategies in empowering CRC patients to actively participate in their own care by managing symptoms, treatments, and the physical as well as psychosocial impacts of the disease. These interventions also support patients in navigating relationships with family, community, nursing and healthcare professionals. By fostering self-efficacy and acceptance, self-management programmes can significantly improve QoL. Integrating digital health technologies increases accessibility, engagement, and personalised support, helping to overcome geographical and logistical barriers. Future research should examine the long-term effects of self-management interventions in diverse populations. Tailoring interventions to individual and cultural needs can enhance effectiveness. Standardised protocols will enable better comparisons and strengthen the evidence base. In conclusion, self- management interventions are essential for improving well-being in CRC patients. Integrating innovative approaches, nursing roles and technology will be key to delivering comprehensive, patient-centred care that addresses both medical and psychosocial needs.
Self-management interventions should be integrated into routine colorectal cancer care to enhance patients’ self-efficacy, symptom management, and quality of life. Tailored programmes that combine psychoeducational, digital, and nurse-led support can address both physical and psychosocial needs effectively. Future efforts must focus on developing standardised, culturally sensitive interventions with longer follow-up to ensure sustainability and broad applicability. Nurses and healthcare providers play a vital role in delivering personalised, evidence-based self- management support to improve patient outcomes.
Regarding this topic, the writers have no conflicts of interest.
The authors acknowledge Universitas Indonesia, Poltekkes Kemenkes Jakarta I, Indonesia and the Ministry of Health, Indonesia for their tremendous support during the study. The authors would also like to say thanks for all respondents who participated in this study.
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