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Clinical Trials/NCT04204447
NCT04204447CompletedNot Applicable

A Prospective Study Showing the Effect of Video Interactive Education on Medical Decision Making in Patients on Opiate Replacement Therapy (ORT) With a History of Hepatitis C

State University of New York at Buffalo2 sites in 1 country176 target enrollmentStarted: November 27, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
176
Locations
2
Primary Endpoint
Improvement in Scores on HCV Knowledge Questionnaire

Study Overview

Brief Summary

The purpose of this study is to determine the most effective way to give patients information regarding hepatitis C virus infection. The investigators plan to compare the information retained by some patients who are given a brochure alone versus patients who watch an interactive video about hepatitis C.

Detailed Description

Subjects will complete 3 questionnaires, including one about knowledge of Hepatitis C. The subject will then either watch a video or read a brochure about Hepatitis C, then take the same questionnaire again. The subject will then return in one month to take the Hepatitis C questionnaire again.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Currently on active treatment for opioid addiction/use
  • •English as primary language

Exclusion Criteria

  • Not provided

Arms & Interventions

Video intervention

Experimental

Subjects will be asked to watch an educational video about Hepatitis C

Intervention: Hepatitis C Educational Video (Other)

Brochure intervention

Experimental

Subjects will be asked to read an educational brochure about Hepatitis C

Intervention: Hepatitis C Educational Brochure (Other)

Outcomes

Primary Outcomes

Improvement in Scores on HCV Knowledge Questionnaire

Time Frame: Pre-intervention, Immediate post-intervention, and 1 mo. follow up

The main outcome measure was a change in the mean score on a 25-item HCV knowledge assessment without subscales. The instrument values ranged from 0 to 25 with one point per correct answer to questions directly arising from the information contained in the video. One point was assigned to each correct answer, and an increase in the score indicated more correct responses.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Andrew Talal

Principal Investigator

State University of New York at Buffalo

Study Sites (2)

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