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Clinical Trials/NCT04889105
NCT04889105
Recruiting
Not Applicable

Enhanced Home-Based Exercise Therapy for Peripheral Arterial Disease Through Mobile Health and Remote Monitoring

VA Office of Research and Development2 sites in 1 country75 target enrollmentDecember 1, 2021

Overview

Phase
Not Applicable
Intervention
Performance evaluation
Conditions
Peripheral Artery Disease
Sponsor
VA Office of Research and Development
Enrollment
75
Locations
2
Primary Endpoint
6-minute walk test
Status
Recruiting
Last Updated
11 days ago

Overview

Brief Summary

Peripheral artery disease (PAD) is a highly prevalent condition affecting up to 10% of Veterans that leads to loss of walking ability and increased risk of amputation. Veterans have limited access to supervised exercise therapy, a facility-based program proven to improve walking ability in PAD, which is poorly attended due to the inconvenience and cost of attending a 12-week program with multiple weekly sessions. This CDA-2 application will investigate the feasibility of home-based exercise therapy (HBET) delivered using mobile health (mHealth) technologies in Veterans with symptomatic PAD. We will partner with the MOVE! program to deliver HBET through group behavioral coaching and a novel wearable activity monitor in a newly proposed program called Smart MOVE!. There is a clear need to provide effective and convenient alternatives to supervised exercise for Veterans with PAD. This study will provide evidence to proceed with Smart MOVE!, a much-needed patient-centered rehabilitation program for Veterans with PAD.

Detailed Description

An estimated 8.5 million Americans (or 7% of US adults) and nearly 10% of veterans are estimated to have peripheral arterial disease (PAD). Significantly debilitating and negatively impacting quality of life, the primary symptom of PAD is claudication (reproducible leg pain with ambulation) that leads to impaired mobility, loss of functional independence, and a heightened risk for amputation. Veterans are at an increased risk of developing symptomatic PAD due to their disproportionately high rates of PAD risk factors such as diabetes, smoking, and hypertension, the most prominent PAD risk factors. Supervised exercise therapy is proven to decrease claudication and enhance mobility in PAD; however, fewer than 25% of eligible patients enroll. Participation in this facility-based program requires travel to a rehabilitation center 3 times per week for 12-weeks, which can be burdensome and costly for Veterans, many of whom live in rural areas and on fixed incomes. There is, therefore, a need to develop a convenient and effective alternative exercise rehabilitation program for Veterans with PAD, particularly in light of safety considerations now associated with this population's travel to group facilities in the current COVID pandemic. A promising approach to increase access to exercise rehabilitation for PAD is remote, home-based exercise therapy (HBET). HBET programs combine self-led walking exercises with health coaching and exercise tracking with a wearable activity monitor. Adapting HBET to PAD is difficult, however, due to the added complexity of an exercise prescription that requires the patient to walk until they experience near-maximal leg pain. Even with active coaching, successfully implementing HBET for PAD with long-term adherence has been difficult in the past. The goal is of this study is to leverage newer mobile health (mHealth) tools to adapt HBET for PAD. This technology-enhanced approach for HBET will be conducted by partnering with a successful VA lifestyle program, MOVE!, which has demonstrated success in achieving sustained weight loss and reduced diabetes onset through lifestyle modification. As increased physical activity is a core element of MOVE!, participation may help increase adherence with HBET for PAD. This newly proposed program, Smart MOVE!, will be a multi-component program featuring a tailored version of MOVE! and a novel mHealth device to improve convenience, access, and adherence to HBET for PAD.

Registry
clinicaltrials.gov
Start Date
December 1, 2021
End Date
September 30, 2026
Last Updated
11 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age \>40 years
  • Eligible Veteran status
  • Clinically stable intermittent claudication ( 2 months of Rutherford Class II symptoms, no evidence of chronic limb-threatening ischemia)
  • Established PAD diagnosis (abnormal ankle-brachial index or evidence of PAD on prior certified vascular laboratory or radiology imaging)
  • Access to safe location to perform walking exercises

Exclusion Criteria

  • Above or below knee amputation
  • critical limb ischemia (rest pain or tissue loss including ulceration or gangrene)
  • inability to walk without a walker
  • wheelchair confinement
  • non-English speaking
  • significant visual impairment that interferes with walking activity
  • hearing impairment that interferes with full study participation
  • unable or unwilling to return to the medical center at the expected visit frequency or unable or unwilling to use the technology required for the intervention
  • Individuals whose walking is limited by a condition other than PAD
  • Any active cardiac condition including unstable angina

Arms & Interventions

Performance evaluation

Preliminary performance evaluation to refine the Smart MOVE! intervention.

Intervention: Performance evaluation

Smart MOVE!

Participants will be enrolled in the multi-component Smart MOVE! intervention for 12 weeks.

Intervention: Smart MOVE!

Usual care

Participants will receive general walking advice for 12 weeks.

Intervention: General walking advice

Outcomes

Primary Outcomes

6-minute walk test

Time Frame: 90 days

The 6MWT is a well-validated measure of functional capacity and increasingly recognized as a meaningful outcome measure in PAD. Participants will be asked to walk back and forth along a 100-foot hallway for six minutes using standard methods and have their total distance recorded

Study Sites (2)

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