Familial Prostate Cancer Clinical Trials

Find Familial Prostate Cancer Clinical Trials Near You

Development and Exploring the Efficacy of a Dyadic Co-learning Intervention for Patients With Prostate Cancer and Their Spouses

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study aims to help patients with prostate cancer and their spouses cope better with the challenges of cancer by learning and supporting each other together. The investigators will test an 8-week Dyadic Co-learning Intervention, which includes weekly learning topics, a mobile app, and professional support. The goal is to improve their physical symptoms, emotional well-being, and resilience. Participants will be randomly assigned to one of two groups. One group will receive regular care, while the other group will receive regular care plus the new co-learning program. The investigators will ask both patients and their spouses to complete questionnaires at the beginning of the study, and again at 10 and 16 weeks, to understand how the program affects their health and well-being.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 90
Healthy Volunteers: f
View:

⁃ For Patients:

• Diagnosed with prostate cancer by a board-certified urologist.

• Has either decided on a treatment plan or completed treatment within the past two years.

• Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.

⁃ For Spouses:

• Must be a cohabiting spouse of the prostate cancer patient and aged 20 years or older.

• Must have a Barthel Index score of 91 or above, indicating good functional independence.

Locations
Other Locations
Taiwan
Keelung Chang Gung Memorial Hospital
NOT_YET_RECRUITING
Keelung
LinKou Chang Gung Memorial Hospital
RECRUITING
Taoyuan District
Contact Information
Primary
Ching-Hui Chien, PhD
chinghui@ntunhs.edu.tw
+886-2-28227101
Time Frame
Start Date: 2025-10-13
Estimated Completion Date: 2026-07-31
Participants
Target number of participants: 60
Treatments
No_intervention: Control Group
Participants in the control group will receive routine care.
Experimental: Dyadic Co-learning Intervention Group
Participants in the experimental group will receive routine care plus an 8-week Dyadic Co-learning Intervention.
Sponsors
Collaborators: Chang Gung Memorial Hospital
Leads: National Taipei University of Nursing and Health Sciences

This content was sourced from clinicaltrials.gov