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

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.

Study Overview

• Status: Recruiting
• Conditions: Aging; Hiv; Physical Inactivity
• Intervention / Treatment: Behavioral: Physical Activity Coaching; Behavioral: Social Support for Physical Activity; Behavioral: Brief Advice and Self-Monitoring; Behavioral: Cognitive Behavioral Intervention for Physical Activity

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 Type: Interventional
• Enrollment (Estimated): 208
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Lisa Uebelacker, PhD; Phone Number: 401-455-6381; Email: luebelacker@butler.org
• Study Contact Backup: Name: Bailey O'Keeffe, MS; Phone Number: 401-455-6219; Email: bokeeffe@butler.org

Study Locations

• United States
  • Minnesota
    • Minneapolis, Minnesota, United States, 54415
      • Recruiting
      • Hennepin Healthcare Research Institute
      • Principal Investigator: Jason Baker, MD
      • Contact: Ashley Black; Phone Number: 612-873-6273
  • Rhode Island
    • Providence, Rhode Island, United States, 02904
      • Recruiting
      • Lifespan Affiliates
      • Contact: Uzma Malik, BA; Phone Number: 401-793-8870
      • Principal Investigator: Megan Pinkston-Camp, PhD

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 50 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

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 antiretroviral therapy (ART) for > 3 months, as assessed via self-report.
3. 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.
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; 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.
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. Capacity to consent, documented by acceptable answers in a consent "teach-back" process.
8. Score of greater than 16 on the MOCA
9. Able to ambulate without assistive devices
10. 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.
  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).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Factorial Assignment
• Masking: Single

Number of Arms

8

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: BASM + PA Coaching; Brief Advice and Self-Monitoring 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 and Self-Monitoring; 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
Experimental: BASM + CB-PA; Brief Advice and Self-Monitoring Cognitive-Behavioral Intervention to Increase Physical Activity	Behavioral: Brief Advice and Self-Monitoring; 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; 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 motivation, depression, and chronic pain. Meetings will occur every other week for 4 months.; Other Names: CB- PA
Experimental: BASM + SS-PA; Brief Advice and Self-Monitoring 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 and Self-Monitoring; 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
Experimental: BASM + PA Coaching + CB-PA; Brief Advice and Self-Monitoring Physical Activity Coaching Cognitive-Behavioral Intervention to Increase Physical Activity	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 and Self-Monitoring; 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; 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 motivation, depression, and chronic pain. Meetings will occur every other week for 4 months.; Other Names: CB- PA
Experimental: BASM + PA Coaching + SS-PA; Brief Advice and Self-Monitoring Physical Activity Coaching Social support for Physical Activity	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: 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 and Self-Monitoring; 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
Experimental: BASM + CB-PA + SS-PA; Brief Advice and Self-Monitoring Cognitive-Behavioral Intervention to Increase Physical Activity 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 and Self-Monitoring; 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; 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 motivation, depression, and chronic pain. Meetings will occur every other week for 4 months.; Other Names: CB- PA
Experimental: BASM + PA Coaching + CB-PA + SS-PA; Brief Advice and Self-Monitoring Physical Activity Coaching Cognitive-Behavioral Intervention to Increase Physical Activity Social support for Physical Activity	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: 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 and Self-Monitoring; 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; 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 motivation, depression, and chronic pain. Meetings will occur every other week for 4 months.; Other Names: CB- PA
Other: BASM; Brief Advice and Self-Monitoring	Behavioral: Brief Advice and Self-Monitoring; 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

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Steps per day	Assessed via Fitbit	Month 4

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Minutes per week of moderate-vigorous activity	Assessed via FitBit	Month 4
Minutes per week of moderate-vigorous activity, self-report	Assessed via the International Physical Activity Questionnaire	Month 4
Frailty Phenotype	Assessed via the Fried Criteria	Month 4
CVD Risk	Assessed using Life's Simple 7 Scale	Month 4
Physical performance	Assessed via the Short Physical Performance Battery	Month 4
Emotional Well-being	Assessed via PROMIS-29 v2.1 profile - Mental Health summary score	Month 4
Physical functioning	Assessed via PROMIS-29 v2.1 profile - Physical Health summary score	Month 4

Collaborators and Investigators

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

Study record dates

Study Major Dates

• Study Start (Actual): June 21, 2023
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): August 31, 2027

Study Registration Dates

• First Submitted: February 22, 2023
• First Submitted That Met QC Criteria: February 22, 2023
• First Posted (Actual): March 2, 2023

Study Record Updates

• Last Update Posted (Actual): November 15, 2023
• Last Update Submitted That Met QC Criteria: November 13, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Other Study ID Numbers: 2208-002

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No