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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01895556
Other study ID # FSG09-Thornton
Secondary ID
Status Completed
Phase N/A
First received June 28, 2013
Last updated July 3, 2013
Start date August 2008

Study information

Verified date July 2013
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to measure the behavioral effects of learning information about male circumcision and HIV risk on sexual behavior and the demand for male circumcision.


Recruitment information / eligibility

Status Completed
Enrollment 1200
Est. completion date
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender Both
Age group 25 Years to 40 Years
Eligibility Inclusion Criteria:

- The study will involve men between the ages of 25 and 40

Exclusion Criteria:

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Other:
Information

Control


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Rebecca Thornton

Outcome

Type Measure Description Time frame Safety issue
Primary Condom use frequency of reported condom use across all sexual acts (never, sometimes, always) One year after baseline survey No
Secondary Male circumcision Circumcision, willingness to circumcise, circumcision of son One year after baseline survey No
Secondary Condom purchases number of condoms purchased one year after baseline survey No
Secondary number of sexual partners number of partners over last year with which individual has engaged in vaginal, anal, oral intercourse one year after baseline survey No
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