Effectiveness Evaluation of a Self-management Program for Prostate Cancer Survivors
Development and Effectiveness Evaluation of a Self-management Program for Prostate Cancer Survivors
1 other identifier
interventional
85
1 country
2
Brief Summary
Objectives: This project aims to develop a self-management program for survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy and determine its effectiveness. Methods: The investigators will develop a self-management program and conduct a study on survivors with prostate cancer experiencing urinary incontinence following radical prostatectomy. And the investigators will test the effectiveness of the self-management program. After completing a pretest, participants will be randomly assigned to the experimental or control group. The self-management group will receive the self-management program for 12 weeks, whereas the information group will receive an information package on a healthy diet. Posttests will be administered 12 and 16 weeks after the pretest. The study variables will include physical symptoms and bothers, cancer-related self-efficacy, social participation, demoralization, and resilience.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2022
Typical duration for not_applicable
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 4, 2022
CompletedFirst Posted
Study publicly available on registry
April 20, 2022
CompletedStudy Start
First participant enrolled
May 20, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2024
CompletedJanuary 3, 2025
September 1, 2023
2.2 years
April 4, 2022
January 2, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Cancer related self-efficacy
The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.
Pre-test
Cancer related self-efficacy
The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.
12 weeks after the pretest
Cancer related self-efficacy
The Mandarin version of the Cancer Survivors' Self-Efficacy Scale (CSSES) will be used to evaluate the cancer-specific self-efficacy of participants.The total score ranges from 11 to 110; the lower the score, the worse the self-efficacy.
16 weeks after the pretest
Secondary Outcomes (12)
Urinary symptoms and bothers
Pre-test
Urinary symptoms and bothers
12 weeks after the pretest
Urinary symptoms and bothers
16 weeks after the pretest
Social participation
Pre-test
Social participation
12 weeks after the pretest
- +7 more secondary outcomes
Other Outcomes (13)
Demographic characteristic and disease information list 1
Pre-test
Demographic characteristic and disease information list 2
Pre-test
Demographic characteristic and disease information list 3
Pre-test
- +10 more other outcomes
Study Arms (2)
Self-management group
EXPERIMENTALThe experimental group will receive the self-management program for 12 weeks.
Information group
OTHERThe control group will receive an information package on a healthy diet.
Interventions
The self-management group will receive the self-management program for 12 weeks, including a self-management application, a self-management manual, and Professional support.
The patients in this group will receive an information package on a healthy diet.
Eligibility Criteria
You may qualify if:
- Prostate cancer survivors will include if they fit the following:
- Received radical prostatectomy and suffering from urinary incontinence for at least one week
- Eastern Cooperative Oncology Group 0-1 point, able to walk entirely independently
- Have a smartphone or a tablet with a wireless network
- Their intimate partner or one of the family members willing to learn together
- Agreed to participate in the study and completed the informed consent form
You may not qualify if:
- Prostate cancer survivors will be excluded if they had one or more of the following:
- A request, with the consideration of family members, that the medical team not tell the patient about the diagnosis or condition of the disease
- A history of psychiatric illness, such as dementia, depression; schizophrenia, or bipolar disorder
- Suffer from other types of cancer and actively undergoing treatment
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Chang Gung Memorial Hospital at Keelung
Keelung, Taiwan
Chang Gung Memorial Hospital at Linkou
Taoyuan District, 33305, Taiwan
Related Publications (26)
Chien CH, Liu KL, Wu CT, Chuang CK, Yu KJ, Lin PH, Huang XY, Pang ST. Development and assessment of a self-management intervention for urinary incontinence among patients with prostate cancer: protocol for a randomized feasibility study. BMC Urol. 2023 Nov 18;23(1):193. doi: 10.1186/s12894-023-01367-7.
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PMID: 12867348BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Ching-Hui Chien, PhD
National Taipei University of Nursing and Health Sciences, Taipei, Taiwan.
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- RN, PhD, Professor
Study Record Dates
First Submitted
April 4, 2022
First Posted
April 20, 2022
Study Start
May 20, 2022
Primary Completion
July 31, 2024
Study Completion
July 31, 2024
Last Updated
January 3, 2025
Record last verified: 2023-09
Data Sharing
- IPD Sharing
- Will not share