AI Article Synopsis
- Urinary incontinence is a frequent issue for prostate cancer patients post-surgery, prompting the creation of a self-management intervention to help them cope.
- The intervention includes a mobile app, a handbook, and professional support, designed to be assessed for feasibility, acceptability, and effectiveness through a controlled study.
- Participants will be randomly assigned to either the self-management program or a control group receiving minimal dietary education, with their progress tracked over a 12 to 16-week period.
Article Abstract
Background: Urinary incontinence is a common complication among patients with prostate cancer who have undergone radical prostatectomy. Guided by social cognitive theory and a framework for the recovery of health and well-being, we propose to develop and test a self-management intervention for patients with prostate cancer who experience urinary incontinence after undergoing radical prostatectomy.
Methods: In this study, a self-management intervention for urinary incontinence (SMI-UI) is developed, comprising a mobile self-management application, a self-management handbook, and professional support. The feasibility, acceptability, and effectiveness of this intervention will be assessed. Patient data from the urology departments of two hospitals will be collected through convenience sampling by adopting an experimental, parallel, and random assignment research design. Patients experiencing urinary incontinence after undergoing radical prostatectomy will be invited to participate. After completing the pretest questionnaire, patients will be randomly divided into the experimental and attention control groups. The experimental group will undergo a 12-week SMI-UI, whereas the attention control group will receive an intervention consisting of a single dietetic education information package. The two groups will be tested 12 and 16 weeks after the pretest. In this study, we recorded the sociodemographic and clinical variables; recruitment rate; retention rate; satisfaction with the intervention; cancer-related self-efficacy; urination symptoms and disturbance; social participation and satisfaction; resilience; and demoralization.
Trial Registration: ClinicalTrials.gov ID: NCT05335967 [date of registration 04-04-2022].
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Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10657576 | PMC |
| http://dx.doi.org/10.1186/s12894-023-01367-7 | DOI Listing |
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