Study of Telemedicine Stress Management and Lifestyle Group Intervention for HCV Patients
- Disease/Condition
- Chronic Hepatitis C
- Drug/Device/Intervention
- VC-CBCS
- Study type
- Interventional
- Intervention type
- behavioral
- Primary sponsor
- University of North Carolina, Chapel Hill
- Location
- Chapel Hill, United States of America
- Phase
- N/A
- Start date
- Apr 10, 2020
- End date
- Feb 24, 2021
- Enrollment
- 32 participants
Percentage of Patients Consented Versus Approached,Percentage of Participants Consented Versus Randomized,Percentage of Standard of Care Condition Participants Retained vs Enrolled,Percentage of VC-CBCS Intervention Condition Participants Retained vs Enrolled,Percentage of Surveys Completed by Participants Who Completed the Study,Global Health Status Physical Health Mean T-Score,Global Health Status Mental Health Mean T-Score,Depression Mean T-score,Anger Mean T-score,Anxiety Mean T-score,Fatigue Mean T-score,Sleep Disturbance Mean T-score,Pain Interference Mean T-score
A pilot feasibility study of a small randomized controlled trial (RCT) comparing a
 video-conferencing cognitive behavioral coping skills (VC-CBCS) group to standard of care
 (SC) for symptomatic patients previously diagnosed with chronic hepatitis C to evaluate
 feasibility, patient satisfaction and differences in symptoms, quality of life and liver
 markers.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT04198584
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT04198584 through Pure Global AI's free database. This phase not specified trial is sponsored by University of North Carolina, Chapel Hill and is currently Completed. The study focuses on Chronic Hepatitis C. Target enrollment is 32 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.