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Clinical Trials/NCT03004170
NCT03004170
Unknown
Not Applicable

Telephone Counseling to Enhance the Quality and Safety of Romantic and Sexual Relationships in People Living and Aging With HIV

Oregon Health and Science University1 site in 1 country343 target enrollmentDecember 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
HIV Seropositivity
Sponsor
Oregon Health and Science University
Enrollment
343
Locations
1
Primary Endpoint
Change in number of condomless sex acts from baseline to 12-month follow-up
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to determine if a brief behavioral intervention delivered over the telephone is effective at reducing occasions of condomless sex in persons living and aging with HIV.

Detailed Description

Estimated rates of condomless anal and vaginal intercourse among HIV-positive older adults remain high. Brief motivational interventions delivered face-to-face have demonstrated efficacy at reducing condomless sex in HIV-positive persons. However, these interventions are not contextualized to the unique sexual health needs of HIV-positive older adults. Further, many HIV-positive older adults have difficulty accessing face-to-face services due to transportation, stigma, and other barriers. Telehealth interventions represent one delivery approach that overcomes such barriers.

Registry
clinicaltrials.gov
Start Date
December 2016
End Date
December 2021
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Travis Lovejoy

Associate Professor of Psychiatry

Oregon Health and Science University

Eligibility Criteria

Inclusion Criteria

  • English speaking
  • Have access to a landline or cellular telephone
  • Be 50 years of age or older at some point during study participation
  • Report engaging in one or more occasions of condomless anal and/or vaginal intercourse with an HIV-negative or unknown HIV serostatus sex partner in the 3 months prior to study enrollment. An exception to this criterion is participants whose HIV viral load is undetectable and whose only condomless sex is in the context of a monogamous sexual relationship with an HIV-negative partner.

Exclusion Criteria

  • Active suicidal ideation as determined by the Patient Health Questionnaire 9-item Depression Module

Outcomes

Primary Outcomes

Change in number of condomless sex acts from baseline to 12-month follow-up

Time Frame: Baseline, 12-month follow-up

Self-reported condomless anal and/or vaginal sex acts with HIV-negative or unknown HIV serostatus sex partners based on the Timeline Followback Interview.

Secondary Outcomes

  • Change in depressive symptom severity from baseline to 12-month follow-up(Baseline, 12-month follow-up)

Study Sites (1)

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