NCT00260780

Brief Summary

Study participants who are exposed to the intervention will: 1)report more condom use during sexual episodes; 2) have fewer new and repeat STD infections 3)demonstrate greater risk reduction, communication, and anger management skills; 4) report fewer substance use behaviors, and 5)report more health care seeking activities, than the participants in the control group

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
300

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jun 2001

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2001

Completed
3 years until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2004

Completed
1.5 years until next milestone

First Submitted

Initial submission to the registry

December 1, 2005

Completed
1 day until next milestone

First Posted

Study publicly available on registry

December 2, 2005

Completed
Last Updated

December 2, 2005

Status Verified

December 1, 2005

First QC Date

December 1, 2005

Last Update Submit

December 1, 2005

Conditions

Keywords

sexually transmitted diseasesRisk Behavior

Outcome Measures

Primary Outcomes (1)

  • Change in risk behaviors

Secondary Outcomes (1)

  • Reported STDs

Interventions

Eligibility Criteria

Age18 Years - 60 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • ages 18 to 60, English speaking, not in jail for sexual offenses (rape or child molestation), reported risk behavior in two months prior to incarceration, weekday and evening availability, viable contact information, self-reported HIV negative status, released from jail no more than 45 days prior, and not visibly under the influence of drugs or alcohol at the time of eligibility determination

You may not qualify if:

  • Opposite of the above

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

STAND, Inc.

Decatur, Georgia, 30335, United States

Location

MeSH Terms

Conditions

Sexually Transmitted DiseasesRisk-Taking

Condition Hierarchy (Ancestors)

Communicable DiseasesInfectionsGenital DiseasesUrogenital DiseasesDisease AttributesPathologic ProcessesPathological Conditions, Signs and SymptomsBehavior

Study Officials

  • Samantha P Williams, Ph.D.

    CDC/NCHSTP/DSTDP/BIRB

    STUDY CHAIR
  • Charles Sperling, M.S.

    STAND, Inc.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
FACTORIAL
Sponsor Type
FED

Study Record Dates

First Submitted

December 1, 2005

First Posted

December 2, 2005

Study Start

June 1, 2001

Study Completion

June 1, 2004

Last Updated

December 2, 2005

Record last verified: 2005-12

Locations