NCT00260754

Brief Summary

Community members within the treatment city will report: 1)engaging in fewer sexual risk practices; 2)significantly higher condom use; 3) significantly higher rates of STD care seeking (including STD screening behaviors); 4) fewer having STDs in the past 6 months; 5) significantly higher awareness scores regarding syphilis and other STDs, as compared with those in the comparison city.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
600

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2002

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

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2002

Completed
2.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2005

Completed
5 months 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

May 31, 2006

Status Verified

December 1, 2005

First QC Date

December 1, 2005

Last Update Submit

May 30, 2006

Conditions

Keywords

Risk behaviorSexually transmitted diseases

Outcome Measures

Primary Outcomes (1)

  • Changes in syphilis morbidity in affected community

Secondary Outcomes (1)

  • Changes in risk behavior and health care seeking behavior

Interventions

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Clients who utilized two community homeless shelters in the affected community. The affected community was one that had significant syphilis morbidity at the onset of the study.

You may not qualify if:

  • None

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Alabama, Birmingham

Birmingham, Alabama, 35294-0022, United States

Location

MeSH Terms

Conditions

Risk-TakingSexually Transmitted Diseases

Condition Hierarchy (Ancestors)

BehaviorCommunicable DiseasesInfectionsGenital DiseasesUrogenital DiseasesDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Samantha Williams, Ph.D.

    CDC/NCHSTP/DSTDP/BIRB

    STUDY CHAIR
  • Diane Grimley, Ph.D.

    University of Alabama at Birmingham

    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

October 1, 2002

Study Completion

July 1, 2005

Last Updated

May 31, 2006

Record last verified: 2005-12

Locations