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Telephone-delivered Behavioral Interventions to Reduce Risky Sexual Behavior in HIV-positive Late Middle-age and Older Adults

Phase 1
Completed
Conditions
Unsafe Sex
Interventions
Behavioral: 1-session of telephone-administered motivational interviewing
Behavioral: 4-session telephone-administered motivational interviewing
Registration Number
NCT01499706
Lead Sponsor
Ohio University College of Osteopathic Medicine
Brief Summary

The number of late middle-age and older adults living with HIV/AIDS in the U.S. continues to rise due largely to

* better clinical care and the improved efficacy of highly active antiretroviral therapy that has extended the lives of many HIV-positive persons

* an increase in the number of new HIV infections in older persons. This study tested the efficacy of 1- and 4-session telephone-administered behavioral sexual risk reduction interventions for HIV-positive adults 45-plus years of age who engage in risky sexual behaviors.

Detailed Description

The number of late middle-age and older adults living with HIV/AIDS in the U.S. continues to rise. In fact, it is estimated that by 2014, 50% of all HIV-positive persons will be 50 years of age or older, due largely to a) better clinical care and the improved efficacy of highly active antiretroviral therapy that has extended the lives of many HIV-positive persons and b) an increase in the number of new HIV infections in older persons. Despite escalating HIV incidence and prevalence rates in older adults, and the fact that an estimated 13% to 30% of older persons living with HIV/AIDS continue to engage in risky sexual practices, few secondary risk reduction interventions have been contextualized to meet the unique needs of sexually active HIV-infected older adults. These unique needs include biological and libidinal changes associated with aging such as erectile dysfunction and the increased use of erectile dysfunction medications in older men, sexual partnerships with younger persons, survivor guilt over outliving romantic partners, and the impact of co-morbid chronic illnesses (e.g., diabetes, osteoporosis, cancer, hepatitis C) and associated medication and/or treatment side effects on perceptions of physical attractiveness.

Many HIV-positive older adults who would benefit from face-to-face sexual risk reduction interventions live with serious comorbid health conditions that complicate travel to medical and social service appointments, have significant confidentiality concerns, and are geographically isolated from traditional risk reduction resources. As such, face-to-face interventions are an unrealistic intervention modality for many members of this group. However, risk reduction interventions delivered using distance technologies, such as regular and cellular telephones, can reach many older adults living with HIV/AIDS.

In response to the lack of age-appropriate risk reduction interventions for HIV-infected older adults who engage in high-risk sex, and the potential of telephone technology to deliver cost-effective risk reduction interventions to this group, this study tested the efficacy of 1- and 4-session telephone-administered behavioral sexual risk reduction interventions for HIV-positive adults 45-plus years of age who engage in risky sexual behaviors.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria
  • HIV-positive
  • English-speaking
  • Access to a land line or cellular telephone
  • Unprotected anal or vaginal intercourse in the past 3 months
Exclusion Criteria
  • Sexual partner of study participant

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1-session motivational interviewing1-session of telephone-administered motivational interviewingParticipants will receive a single session of motivational interviewing delivered over the telephone
4-session motivational interviewing4-session telephone-administered motivational interviewingParticipants will receive four weekly sessions of motivational interviewing delivered over the telephone.
Primary Outcome Measures
NameTimeMethod
Change in self-reported number of non-condom-protected anal and vaginal sex acts in the past 3 months from baseline to 6-month follow-upbaseline, 6-month follow-up
Change in self-reported number of non-condom-protected anal and vaginal sex acts in the past 3 months from baseline to 3-month follow-upbaseline, 3-month follow-up
Secondary Outcome Measures
NameTimeMethod
Proportion of participants reporting 100% condom use for anal and vaginal sex in the past 3 months3-month follow-up, 6-month follow-up

Trial Locations

Locations (1)

Ohio University College of Osteopathic Medicine

🇺🇸

Athens, Ohio, United States

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