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Clinical Trial Summary

The objective of this protocol is to conduct a comprehensive quantitative and qualitative assessment of the impact of our innovative collaborative telehealth HCV care model on patient treatment experiences and quality of life.


Clinical Trial Description

The investigators will evaluate the proportion of patients at each step of the HCV care cascade before and after implementation of the collaborative care model. Additionally, participants will complete questionnaires at three time points: at the initiation of hepatitis C treatment, at treatment completion, and at the assessment of sustained virologic response. Questionnaires will assess quality of life, mental health, chronic liver disease outcomes, and substance use. A subset of participants will also complete semi-structured interviews at each of the three time points. Then, a smaller subset of participants will be selected for a detailed ethnographic case study focusing on treatment experiences, quality of life, forms of social support, and illness experience. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03876470
Study type Observational
Source University of Virginia
Contact Rebecca Dillingham, MD
Phone 4349820103
Email RD8V@hscmail.mcc.virginia.edu
Status Not yet recruiting
Phase
Start date May 15, 2019
Completion date November 30, 2020

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