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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01621412
Other study ID # RSAD-VIH-2011
Secondary ID
Status Completed
Phase N/A
First received May 31, 2012
Last updated December 21, 2015
Start date April 2012
Est. completion date June 2013

Study information

Verified date December 2015
Source Policlinique Médicale Universitaire
Contact n/a
Is FDA regulated No
Health authority Switzerland: Ethikkommission
Study type Observational

Clinical Trial Summary

The investigators believe that disclosure of HIV status could influence medication adherence. If disclosure leads to social support, adherence could be improved. This study purpose is to assess correlation between disclosure and medication adherence, and to describe people whose HIV status has been disclosed to.


Description:

Pharmacists administer a questionnaire to each consecutive subject taking part in the adherence-enhancing program at the pharmacy of the Department of Ambulatory Care And Community Medicine in Lausanne. This questionnaire assesses disclosure, response to disclosure, and living situation.

Adherence is measured by electronic monitoring and pill count.


Recruitment information / eligibility

Status Completed
Enrollment 120
Est. completion date June 2013
Est. primary completion date June 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- HIV Infection

- Enrolled in the adherence-enhancing program

Exclusion Criteria:

- Inclusion visit

- Not french or english speaker

Study Design

Observational Model: Cohort, Time Perspective: Cross-Sectional


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Policlinique Médicale Universitaire Lausanne Vaud

Sponsors (3)

Lead Sponsor Collaborator
Policlinique Médicale Universitaire Centre Hospitalier Universitaire Vaudois, Swiss HIV Cohort Study

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Patient Adherence Electronic monitoring of adherence during 30 days before survey 30 days before survey No
Secondary Patient Adherence Electronic monitoring of adherence during 90 days before survey 90 days before survey No
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