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NCT Number: NCT05752500

Optimization of a Behavioral Intervention to Increase Physical Activity in Older Adults Living With HIV

The goal of this clinical trial is to examine 3 interventions designed to increase physical activity in older adults with HIV. We will examine 3 potential components of an intervention package: physical activity coaching, cognitive behavioral therapy targeted toward common barriers to physical activity such as low motivation or chronic pain, and a Fitbit-based social support intervention. Our primary outcome will be physical activity, defined as steps per day. Results will guide choice of intervention components to be used in an optimized behavioral intervention.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hennepin Healthcare Research Institute, Minneapolis, Minnesota, United States

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About this study

Increasing numbers of persons living with HIV (PLWH) are living to older ages. Older PLWH are at increased risk for a wide spectrum of co-morbid conditions such as cardiovascular disease, frailty phenotype, and mental health disorders. Practical primary care-based interventions are needed for older PLWH that target lifestyle factors to reduce complications of aging and improve healthspan. Most PLWH engage in less physical activity (PA) than is recommended by public health guidelines. Thus, increasing PA can lead to numerous mental and physical health benefits among PLWH. Current studies in PLWH typically focus on the impact of supervised exercise. However, there are many barriers to this type of PA. Lifestyle physical activity (LPA) programs that focus on integrating PA, especially walking, into everyday life, may be more successful in producing a sustained increase in PA. The long-term goal of this research is to develop an effective and efficient primary care intervention that increases LPA among older PLWH. We leverage the Multiphase Optimization STrategy (MOST) as a framework for developing, optimizing, and evaluating a multicomponent behavioral intervention. MOST is comprised of three phases. First, in the preparation phase, an empirical and theory-driven conceptual model is developed that identifies differentiable intervention components and specifies optimization criteria (i.e., goal of intervention development). We have completed this phase. Second, in the optimization phase, the impact of each intervention component on the desired outcome is empirically examined. The goal is to determine which components to include in a final intervention package that is optimized for efficacy and efficiency. The proposed study reflects the second phase, or an optimization trial. Finally, in the evaluation phase, the optimized intervention package is evaluated for efficacy in a traditional RCT; this will be the next step in this line of research following the currently proposed project. In this project, we will test the impact of three separable intervention components on steps per day after 4 months of intervention. We will recruit 196 PLWH of age ≥50 year classified as low-active. All participants receive component '0': brief advice to exercise and a Fitbit activity tracker. We then test 3 additional components in a factorial design: 1) PA Coaching-focused on goal-setting and self-monitoring; 2) Cognitive-Behavioral intervention for PA (CB-PA)-focused on identifying values and addressing internal barriers to PA such as pain, depression, or fatigue; 3) Social Support for PA (SS-PA)-a component which leverages the social functionality of the Fitbit app, promoting social support and friendly competition. The primary outcome will be steps per day during Month 4. The observed main and interaction effects for the 3 candidate components will guide selection of components to be included in an optimized intervention that will be tested in a future RCT. We will also examine potential mediators for each intervention component, as well as secondary outcomes including perceived physical health, mental health, cardiovascular disease risk, and the frailty phenotype.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • HIV positive: defined by HIV antibody, detectable HIV RNA in plasma, or a note from the participant's HIV care provider.
  • Must be on continuous antiretroviral therapy (ART) for > 3 months, as assessed via self-report.
  • Low PA: defined as self-report of < 90 minutes of moderate-vigorous PA (MVPA) per week in the previous 3 months AND less than 14 hours per week of sustained walking in the previous 4 weeks.
  • Medically cleared for moderate PA. If participants report a) a history of cardiovascular disease including known coronary artery disease, peripheral vascular disease, heart failure, or stroke; or b) chest pain, shortness of breath, or dizziness or syncope either at rest or during activity in the past 3 months, then they must have medical clearance by a physician or primary care provider.
  • Age 50 years or older.
  • Proficiency in English: sufficient to engage in informed consent, understand assessments and materials provided, and engage and use Fitbit application (all materials provided in English).
  • Capacity to consent, documented by acceptable answers in a consent "teach-back" process.
  • Score of greater than 16 on the MOCA
  • Able to ambulate without assistive devices
  • Ability to use the FitBit application, as demonstrated to study staff.

Exclusion criteria

  • Exclusion Criteria
  • Medical conditions or physical or neurocognitive limitations that interfere with PA or study participation.
  • Hazardous substance use, assessed via a score ≥15 on the Alcohol Use Disorders Identification Test (AUDIT) or ≥6 on the Drug Abuse Screening Test (DAST).

Treatment and study plan

Cognitive Behavioral Intervention for Physical Activity

Behavioral

Interventionist will use cognitive and behavioral techniques to help the participant increase facilitators and decrease barriers to physical activity, particularly barriers such as lack of motivation, depression, and chronic pain. Meetings will occur every other week for 4 months.

Other names: CB- PA

Social Support for Physical Activity

Behavioral

This component will leverage the social functionality of the Fitbit app, promoting social support and friendly competition via a moderated Facebook group.

Other names: SS-PA

Physical activity coaching

Behavioral

The PA coach will meet with the participant to set goals for physical activity (steps) and encourage self-monitoring. Meetings will occur every other week for 4 months.

Other names: PA Coaching

Brief Advice and Self-Monitoring

Behavioral

Participants will receive a single session with brief advice about increasing physical activity, and instructions on how to use their study-provided FitBit.

Other names: BASM

Primary outcomes

  1. Steps per day

    Time frame: Month 4

    Assessed via Fitbit

Secondary outcomes

  1. Minutes per week of moderate-vigorous activity

    Time frame: Month 4

    Assessed via FitBit

  2. Minutes per week of moderate-vigorous activity, self-report

    Time frame: Month 4

    Assessed via the International Physical Activity Questionnaire

  3. Frailty Phenotype

    Time frame: Month 4

    Assessed via the Fried Criteria

  4. CVD Risk

    Time frame: Month 4

    Assessed using Life's Simple 7 Scale

  5. Physical performance

    Time frame: Month 4

    Assessed via the Short Physical Performance Battery

  6. Emotional Well-being

    Time frame: Month 4

    Assessed via PROMIS-29 v2.1 profile - Mental Health summary score

  7. Physical functioning

    Time frame: Month 4

    Assessed via PROMIS-29 v2.1 profile - Physical Health summary score

Study contacts

Contact information is provided by the study sponsor or research team.

Bailey O'Keeffe, MS

CONTACT

[email protected]

401-455-6219

Lisa Uebelacker, PhD

CONTACT

[email protected]

401-455-6381

Sponsors and collaborators

Lead sponsor

Butler Hospital

Other

Registry information

Acronym: HiActivity

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Mar 2, 2023
Registry last updated
Mar 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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