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NCT03320889 Clinical Trial

Hepatitis C Education for Pregnant Women With Opiate Dependence - Phase 2

Hepatitis C Clinical Trial

Official title:
Hepatitis C Education for Pregnant Women With Opiate Dependence - Phase 2

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03320889
Other study ID # 17-057
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 30, 2017
Est. completion date August 26, 2019

Study information
Verified date August 2019
Source TriHealth Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to assess patients' attitudes and knowledge of Hepatitis C, analyze the variables that may influence patients' knowledge, and educate patients on Hepatitis C.

Description:

The study will compare the effectiveness of providing HCV education by providing a pamphlet and expert education compared to providing a pamphlet only. The information gained in completing this study will help the medical community improve patient education on the disease and specifically understand how the medical community can best serve pregnant patients with opiate dependence burdened by Hepatitis C.

Recruitment information / eligibility
Status Completed
Enrollment 115
Est. completion date August 26, 2019
Est. primary completion date August 26, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Study population includes Faculty Medical Center obstetrics and postpartum patients enrolled in the HOPE program who are 18 years old or older.

- The study will include patients with and without a Hepatitis C diagnosis.

- Patients will be recruited at their routine office visits and/or during any admissions to the hospital.

Exclusion Criteria:

- Patients who do not speak and understand English.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Educational Intervention
Patients will be randomized to a group that receives the pamphlets only and a group that receives the pamphlets and has an expert educator review that pamphlets with them and answer questions.

Locations
Country Name City State
United States Good Samaritan Hospital Cincinnati Ohio

Sponsors (1)
Lead Sponsor Collaborator
TriHealth Inc.

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Number of Questions Scored Correct on the Hepatitis C Knowledge Survey Number of questions scored correct on the Hepatitis C knowledge survey 2-8 weeks after study intervention
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