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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT01234103
Date of registration: 03/11/2010
Primary sponsor: Department of Defense
Public title: Preventing Health Damaging Behaviors in Male and Female Army Recruits
Scientific title: Preventing Health Damaging Behaviors in Male and Female Army Recruits
Date of first enrolment: September 2010
Target sample size: 1000
Recruitment status: Recruiting
URL:  http://clinicaltrials.gov/show/NCT01234103
Study type:  Interventional
Study design:  Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention  
Countries of recruitment
United States
Contacts
Name:   Cherrie B Boyer, PhD
Address: 
Telephone: 415-502-4689
Email: BoyerC@peds.ucsf.edu
Affiliation: 
Name:   Cherrie B Boyer, PhD
Address: 
Telephone: 415-476-9620
Email: boyerc@peds.ucsf.edu
Affiliation: 
Name:   Cherrie B Boyer, PhD
Address: 
Telephone:
Email:
Affiliation:  University of California, San Francisco
Key inclusion & exclusion criteria

Inclusion Criteria:

- All participants will be 18 years of age or older, will be fluent in English, and
able to provide written, informed consent.

Exclusion Criteria:

- AIT soldiers under the age of 18 will be excluded since it will be difficult to
obtain parental consent. We anticipate that this exclusion will be rare.



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Alcohol and Other Substance Use Prevention
Intimate Partner Violence Prevention
Sexual Risk Reduction
Sexually Transmitted Infection (STI) Prevention
Unintended Pregnancy Prevention
Intervention(s)
Behavioral: Staying Safe & In Control: Increasing Knowledge and Building Skills to Prevent STIs and Unintended Pregnancy
Primary Outcome(s)
incidence of sexually transmitted infections and the self-reported numbers of unintended pregnancies [Time Frame: 6 to 9 months]
Secondary Outcome(s)
self-reported behavioral measures related to STI/HIV prevention [Time Frame: 6 to 9 months]
Secondary ID(s)
W81XWH-04-1-0159
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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