Completed

Preparation for HIV Vaccine Trials: Assessing Risk Behaviors and HIV Infection Status

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
What is being tested

Vaccine preparedness

Behavioral
Who is being recruted

Blood-Borne Infections+13

+ Urogenital Diseases

+ Genital Diseases

Over 18 Years
+30 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
See protocol details

Summary

Principal SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Vaccine preparedness studies are necessary in order to prepare for launching preventive HIV vaccine efficacy trials. It is important to gather information on the risk of HIV infection among recruited populations, the extent and stability of HIV risk behaviors in these populations, and the risk of HIV infection associated with risk behaviors. This vaccine preparedness study is designed to expand the capacity of the HIVNET to implement HIV prevention trials, increase the diversity of its participant population, and further target populations at highest risk of HIV infection. Participants complete a total of 6 scheduled study visits: 2 at baseline, 2 at follow-up 6 months later, and 2 at follow-up 12 months after enrollment. Participant risk behaviors and knowledge of and attitudes toward HIV vaccine and other HIV prevention trials are assessed at each time point. HIV infection status is tested by standard HIV ELISA and Western blot at follow-up, as well as at participant request throughout the study. Participants are instructed to recognize and report suspected primary HIV infection based on symptoms or high-risk exposures. HIV pre-test, risk reduction, and post-test counseling is provided in accordance with CDC standards of practice. Participants who become infected with HIV during the study are counseled and referred for medical and psychosocial services.

Principal SponsorNational Institute of Allergy and Infectious Diseases (NIAID)
Last updated: June 24, 2005
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

4892 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Over 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Blood-Borne InfectionsUrogenital DiseasesGenital DiseasesCommunicable DiseasesImmunologic Deficiency SyndromesImmune System DiseasesInfectionsRetroviridae InfectionsRNA Virus InfectionsSexually Transmitted DiseasesVirus DiseasesSexually Transmitted Diseases, ViralLentivirus InfectionsBehaviorRisk-TakingHIV Infections

Criteria

24 inclusion criteria required to participate
- Anal intercourse (receptive or insertive) with one or more other men in the last year

- Diagnosis of syphilis, chlamydia, gonorrhea, first episode herpes, pelvic inflammatory disease, and/or trichomoniasis in the last year

- Exchange of sex for money or drugs in the last year

- HIV-positive through HIVNET testing or HIV-seronegative by EIA

Show More Criteria

6 exclusion criteria prevent from participating
An obvious psychological or psychiatric disorder that would preclude provision of informed consent or otherwise contraindicate study participation

Any condition which in the opinion of the principal investigator would interfere with achieving the study objectives

Currently have a single HIV-seronegative partner with whom they have been in a mutually monogamous relationship for at least 2 years. (Men at risk through anal intercourse only)

Currently obtain over 50 percent of needles/syringes for injection of drugs from a needle exchange program. (Men and women at risk through injection only)

Show More Criteria

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 8 locations

Los Angeles County / Health Research Assoc / Drew Med Ctr

Los Angeles, United StatesOpen Los Angeles County / Health Research Assoc / Drew Med Ctr in Google Maps

Univ of Illinois Hosp at Chicago

Chicago, United States

Johns Hopkins Univ

Baltimore, United States

New York Univ Med Ctr

New York, United States
Completed8 Study Centers