Efficacy of a Couple-Focused mHealth Symptom Self-management Program
Last updated on July 2021Recruitment
- Recruitment Status
- Active, not recruiting
- Estimated Enrollment
- 500
Summary
- Conditions
- Prostate Cancer
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Triple (Care Provider, Investigator, Outcomes Assessor)Masking Description: The investigator and data collectors will be masked to intervention.Primary Purpose: Supportive Care
Participation Requirements
- Age
- Between 40 years and 75 years
- Gender
- Both males and females
Description
This randomized clinical trial aims to test the efficacy of a couple-focused, web-based tailored prostate cancer symptom management program, Prostate Cancer Education and Resources for Couples (PERC). The study participants will include 300 patients completing initial treatment for localized prostat...
This randomized clinical trial aims to test the efficacy of a couple-focused, web-based tailored prostate cancer symptom management program, Prostate Cancer Education and Resources for Couples (PERC). The study participants will include 300 patients completing initial treatment for localized prostate cancer and their intimate partners (i.e., 300 dyads and 600 individuals). After informed consent, we will conduct baseline assessment (T1), randomly assign eligible participants to either PERC or the National Cancer Institute (NCI) website, and then collect data at 4 (T2), 8 (T3), and 12 months (T4) post-T1.
Tracking Information
- NCT #
- NCT03489057
- Collaborators
- National Institute of Nursing Research (NINR)
- Investigators
- Principal Investigator: Lixin (Lee) Song, RN, PhD University of North Carolina, Chapel Hill
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