COMPLETED

STI/HIV Intervention Behavioral Intervention Program

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Conditions

Sexually Transmitted InfectionsSTIHIVsyphilisgonorrheachlamydiamycoplasma genitalium

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The hypothesis is that a behavioral intervention tool adapted for the US military population will be acceptable and associated with a decrease in incident sexually transmitted infection (STI)/HIV rates and high-risk sexual behaviors, and increased self-reported condom use compared to the standard of care at the Joint Base Lewis-McChord (JBLM) Preventive Medicine clinic and the Fort Bragg Department of Public Health (part of Womack Army Medical Center).

Official Title

Prospective Cohort Trial To Assess Acceptability and Efficacy of an Adapted STI/HIV Intervention Behavioral Intervention Program in a Population of US Army Personnel and Their Medical Beneficiaries - Execution Phase

Quick Facts

Study Start:2020-11-04
Study Completion:2024-03-10
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT04547413

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 30 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 18 - 30 years
  2. 2. Army active duty or Army medical beneficiary
  3. 3. Eligible to receive care at a military healthcare clinic for at least 12 months from enrollment
  4. 4. HIV negative
  5. 5. Not scheduled for military deployment or transfer within 3 months of enrolment
  6. 6. Not pregnant, regardless of marital status
  7. 7. Not trying to become pregnant or impregnate a partner, regardless of marital status
  8. 8. Be classified as "high risk" either through a positive STI diagnosis in the last 180 days or has had STI screening during this timeframe.
  9. 9. Self reports vaginal, oral, and/or anal sexual contact in the last 30 days.
  1. 1. Under 18 or over 30 years of age
  2. 2. Not Army active duty or Army medical beneficiary
  3. 3. Not eligible to receive care at a military healthcare clinic for study duration (next 12 months)
  4. 4. HIV positive
  5. 5. Military deployment or transfer scheduled within 3 months of enrollment
  6. 6. Are pregnant, regardless of marital status
  7. 7. Are trying to become pregnant or impregnate someone, regardless of marital status
  8. 8. Has not had a positive STI diagnosis or STI screening within the last 180 days
  9. 9. Does not self-report vaginal, anal, and/or oral sexual contact in the last 30 days

Contacts and Locations

Principal Investigator

Tatjana Calvano, MD
PRINCIPAL_INVESTIGATOR
Madigan Army Medical Center

Study Locations (Sites)

Ft. Bragg
Fayetteville, North Carolina, 28310
United States
Madigan Army Medical Center
Tacoma, Washington, 98431
United States

Collaborators and Investigators

Sponsor: Madigan Army Medical Center

  • Tatjana Calvano, MD, PRINCIPAL_INVESTIGATOR, Madigan Army Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-11-04
Study Completion Date2024-03-10

Study Record Updates

Study Start Date2020-11-04
Study Completion Date2024-03-10

Terms related to this study

Keywords Provided by Researchers

  • STI
  • HIV
  • syphilis
  • gonorrhea
  • chlamydia
  • mycoplasma genitalium

Additional Relevant MeSH Terms

  • Sexually Transmitted Infections