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

Sponsor
Butler Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05752500
Collaborator
(none)
208
8
42

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behavioral Intervention for Physical Activity
  • Behavioral: Social Support for Physical Activity
  • Behavioral: Physical Activity Coaching
  • Behavioral: Brief Advice + a physical activity tracker
N/A

Detailed Description

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 208 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
208 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
2x2x2 factorial design2x2x2 factorial design
Masking:
Single (Investigator)
Masking Description:
Data analyst will be masked to intervention component assignment labels.
Primary Purpose:
Treatment
Official Title:
Optimization of a Behavioral Intervention to Increase Physical Activity in Older Adults Living With HIV
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Oct 1, 2026
Anticipated Study Completion Date :
Dec 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: BA + PA Coaching

Brief Advice to Engage in Physical Activity + FitBit Physical Activity Coaching

Behavioral: Physical Activity Coaching
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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + CB-PA

    Brief Advice to Engage in Physical Activity + FitBit Cognitive-Behavioral Intervention to Increase Physical Activity

    Behavioral: Cognitive Behavioral Intervention for Physical Activity
    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 motivatoin, depression, and chronic pain. Meetings will occur every other week for 4 months.
    Other Names:
  • CB- PA
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + SS-PA

    Brief Advice to Engage in Physical Activity + FitBit Social support for Physical Activity

    Behavioral: Social Support for Physical Activity
    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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + PA Coaching + CB-PA

    Brief Advice to Engage in Physical Activity + FitBit Physical Activity Coaching Cognitive-Behavioral Intervention to Increase Physical Activity

    Behavioral: Cognitive Behavioral Intervention for Physical Activity
    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 motivatoin, depression, and chronic pain. Meetings will occur every other week for 4 months.
    Other Names:
  • CB- PA
  • Behavioral: Physical Activity Coaching
    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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + PA Coaching + SS-PA

    Brief Advice to Engage in Physical Activity + FitBit Physical Activity Coaching Social support for Physical Activity

    Behavioral: Social Support for Physical Activity
    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
  • Behavioral: Physical Activity Coaching
    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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + CB-PA + SS-PA

    Brief Advice to Engage in Physical Activity + FitBit Cognitive-Behavioral Intervention to Increase Physical Activity Social support for Physical Activity

    Behavioral: Cognitive Behavioral Intervention for Physical Activity
    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 motivatoin, depression, and chronic pain. Meetings will occur every other week for 4 months.
    Other Names:
  • CB- PA
  • Behavioral: Social Support for Physical Activity
    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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Experimental: BA + PA Coaching + CB-PA + SS-PA

    Brief Advice to Engage in Physical Activity + FitBit Physical Activity Coaching Cognitive-Behavioral Intervention to Increase Physical Activity Social support for Physical Activity

    Behavioral: Cognitive Behavioral Intervention for Physical Activity
    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 motivatoin, depression, and chronic pain. Meetings will occur every other week for 4 months.
    Other Names:
  • CB- PA
  • Behavioral: Social Support for Physical Activity
    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
  • Behavioral: Physical Activity Coaching
    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
  • Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Other: BA

    Brief Advice to Engage in Physical Activity + FitBit

    Behavioral: Brief Advice + a physical activity tracker
    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:
  • BA
  • Outcome Measures

    Primary Outcome Measures

    1. Steps per week [Month 4]

      Assessed via Fitbit

    Secondary Outcome Measures

    1. Minutes per week of moderate-vigorous activity [Month 4]

      Assessed via FitBit

    2. Minutes per week of moderate-vigorous activity, self-report [Month 4]

      Assessed via the International Physical Activity Questionnaire

    3. Frailty Phenotype [Month 4]

      Assessed via the Fried Criteria

    4. CVD Risk [Month 4]

      Assessed using Life's Simple 7 Scale

    5. Physical performance [Month 4]

      Assessed via the Short Physical Performance Battery

    6. Emotional Well-being [Month 4]

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

    7. Physical functioning [Month 4]

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

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    50 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. HIV positive: defined by HIV antibody, detectable HIV RNA in plasma, or a note from the participant's HIV care provider.

    2. Must be on continuous antiretrotroviral therapy (ART) for > 3 months, as assessed via self-report. Any participant not on continuous ART should have this as the main focus of their treatment.

    3. Low PA: defined as self-report of < 90 minutes of moderate-vigorous PA (MVPA) per week in the previous 3 months. NOTE: This is easily ascertained during a screener and ensures enrollment of a population that needs to increase PA.

    4. 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; b) diabetes; or c) 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.

    5. Age 50 years or older.

    6. 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).

    7. Cognitive capacity: sufficient to provide consent, documented by acceptable answers in a consent "teach-back" process.

    8. Able to ambulate without assistive devices

    9. Ability to use the FitBit application, as demonstrated to study staff.

    Exclusion Criteria:
    • Exclusion Criteria
    1. Medical conditions or physical or neurocognitive limitations that interfere with PA or study participation. Participants will be excluded if, in the opinion of an investigator or primary provider, participation in the study would be unsafe, not possible, or not in the participant's best interest.

    2. 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).

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Butler Hospital

    Investigators

    • Principal Investigator: Lisa Uebelacker, PhD, Butler Hospital
    • Principal Investigator: Jason Baker, MD, Hennepin Healthcare

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Butler Hospital
    ClinicalTrials.gov Identifier:
    NCT05752500
    Other Study ID Numbers:
    • 2208-002
    First Posted:
    Mar 2, 2023
    Last Update Posted:
    Mar 2, 2023
    Last Verified:
    Feb 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No

    Study Results

    No Results Posted as of Mar 2, 2023