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Community Walking Exercise for Patients With Peripheral Artery Disease (GAIT)

Primary Purpose

Peripheral Artery Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Exercise therapy
lower extremity ET
peripheral open intervention
Sponsored by
University of Minnesota
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Artery Disease focused on measuring claudication, community walking exercise, community-based participatory research, exercise adherence, endovascular therapy

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women diagnosed with atherosclerotic PAD
  • ≥40 years of age
  • An abnormal ankle-brachial index (ABI) of ≤.90
  • For patients with an ABI >.90 and <1.00, a post-exercise ABI drop of 15% or more compared to the resting ABI
  • Patients receiving lower extremity ET or peripheral open intervention
  • Patients not receiving lower extremity ET or peripheral open intervention but present with stable claudication and an abnormal ABI

Exclusion Criteria:

  • Lower extremity amputation(s), including a toe amputation, which interfere (s) with walking on the treadmill
  • Individuals with critical limb ischemia defined by ischemic rest pain or ischemic ulcers/gangrene on the lower extremities
  • PAD of non-atherosclerotic nature (e.g., fibromuscular dysplasia, irradiation, endofibrosis)
  • Coronary artery bypass grafts or major surgical procedures within 6 months prior to screening
  • Individuals whose walking exercise is primarily limited by symptoms of chronic obstructive pulmonary disease, angina, or heart failure
  • Individuals who are unable to walk on the treadmill at a speed of at least 2 mph for at least 1 minute
  • Individuals who have had a myocardial infarction within 3 months prior to screening
  • Individuals who demonstrate symptoms consistent with acute coronary syndrome
  • Individuals who exhibit ischemia as documented on the 12-lead electrocardiogram including horizontal or down-sloping ST-segment depression ≥0.5 mm at rest and >1 mm with exercise in 2 contiguous leads, relative to the PR-segment (ST-segment measured 0.08 seconds after the J point, ST-segment elevation ≥1 mm)
  • Individuals who have had a transient ischemic attack or stroke 3 months prior to screening
  • Individuals with left bundle branch block or sustained ventricular tachycardia (>30 sec) during screening
  • Individuals with uncontrolled hypertension (≥180 systolic or ≥100 diastolic resting blood pressure) during screening
  • Treatment with pentoxifylline or cilostazol for the treatment of claudication 4 weeks prior to screening; Patients can be reconsidered for study inclusion following a 1 month washout period from these medications
  • Electrolyte abnormalities (e.g., potassium <3.3 mmol∙Lˉ1 )
  • Pregnancy, fertility without protection against pregnancy (for women of childbearing potential, a serum pregnancy test will be performed at screening)
  • Incarcerated individuals
  • Individuals acutely impaired by alcohol or other illicit drugs
  • Poorly controlled diabetes defined as glycated hemoglobin >12%
  • Severely anemic patients (Hgb <11 g∙dLˉ1 for women and <10 g∙dLˉ1 for men)
  • For patients who have not received peripheral revascularization, an ABI of >0.90
  • For patients with equivocal resting ABIs (0.91-0.99), a drop of <15% in the post-exercise ABI
  • For individuals with non-compressible vessels (ABI >1.39) who have a toe- brachial index (TBI) >0.70
  • Inability to speak English
  • Other clinically significant disease that is, in the opinion of the study team, not stabilized or may otherwise confound the results of the study

Sites / Locations

  • International Heart Institute of Montana Foundation

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Experimental

Placebo Comparator

Arm Label

Exercise therapy

Exercise advice

lower extremity ET, exercise therapy

lower extremity ET, exercise advice

Peripheral open intervention, exercise therapy

Peripheral open intervention, exercise advice

Arm Description

Claudication, no peripheral revasc

Claudication, no peripheral revasc

Outcomes

Primary Outcome Measures

Change in peak walking time (PWT)

Secondary Outcome Measures

Change in claudication onset time (COT)
Change in patient-reported outcomes
Change in peak oxygen uptake
Change in functional ability
Functional ability will be assessed with the 6-min walk test and Short Physical Performance Battery which consists of 1) walking short distances, 2) completing balance tests and 3) sit and standing from a chair 5 times.
Evaluation of total volume of activity
Evaluation of exercise adherence
For patients randomized to the exercise therapy group

Full Information

First Posted
February 13, 2014
Last Updated
April 20, 2020
Sponsor
University of Minnesota
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02075502
Brief Title
Community Walking Exercise for Patients With Peripheral Artery Disease
Acronym
GAIT
Official Title
A Community-based Exercise Program to Improve Walking Outcomes in Patients With Peripheral Artery Disease
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
February 1, 2014 (Actual)
Primary Completion Date
February 12, 2020 (Actual)
Study Completion Date
February 12, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
Collaborators
National Institutes of Health (NIH), National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary aim of the study is to determine the effect of a community-based walking exercise program with detailed training, monitoring, and coaching (TMC) exercise components enhanced by community-based participatory research (CBPR) practices (TMC+) on the primary outcome of peak walking time (PWT) in patients with peripheral artery disease (PAD).
Detailed Description
The investigators will test the hypothesis that PAD patients randomized to the exercise program in the community setting incorporating TMC+ will improve walking ability compared with patients who receive the standard of care (exercise advice). Secondary hypotheses include a significant improvement in patient-reported outcomes, an improvement in functional ability or a significant increase in volume of physical activity for patients who complete community-based walking exercise when compared with patients receiving the standard of care. Exploratory hypotheses include a significant improvement in PWT for 1) patients receiving a combination of lower extremity endovascular therapy (ET) and community-based walking exercise or 2) open peripheral intervention and community-based walking exercise compared to patients who do not receive endovascular therapy or open intervention and receive only the standard of care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Artery Disease
Keywords
claudication, community walking exercise, community-based participatory research, exercise adherence, endovascular therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise therapy
Arm Type
Experimental
Arm Description
Claudication, no peripheral revasc
Arm Title
Exercise advice
Arm Type
Placebo Comparator
Arm Description
Claudication, no peripheral revasc
Arm Title
lower extremity ET, exercise therapy
Arm Type
Experimental
Arm Title
lower extremity ET, exercise advice
Arm Type
Placebo Comparator
Arm Title
Peripheral open intervention, exercise therapy
Arm Type
Experimental
Arm Title
Peripheral open intervention, exercise advice
Arm Type
Placebo Comparator
Intervention Type
Behavioral
Intervention Name(s)
Exercise therapy
Intervention Description
The exercise therapy program with training, monitoring and coaching enhanced by community-based participatory research (CBPR) (TMC+) is a comprehensive approach to community-based walking exercise for improving PAD patient outcomes. The components of TMC+ are optimal training guidelines for patients (i.e., T), monitoring from both investigators and patient self-monitoring (i.e., M), coaching from investigators on how to improve patients' walking ability (i.e., C), and finally enhancements from CBPR practices (+).
Intervention Type
Procedure
Intervention Name(s)
lower extremity ET
Intervention Description
catheter-based revascularization of peripheral arteries (background treatment part of standard clinical care at hospital)
Intervention Type
Procedure
Intervention Name(s)
peripheral open intervention
Intervention Description
revascularization of lower extremities with open bypass surgery (background treatment part of standard clinical care at hospital)
Primary Outcome Measure Information:
Title
Change in peak walking time (PWT)
Time Frame
Baseline, post-revascularization (ET or open intervention) (4 weeks, if applicable), post-12 weeks (exercise and control groups), 6 months following intervention time period
Secondary Outcome Measure Information:
Title
Change in claudication onset time (COT)
Time Frame
Baseline, post-revascularization (ET or open intervention), post-12 weeks (exercise and control groups), 6 months following intervention time period
Title
Change in patient-reported outcomes
Time Frame
Baseline, post-revascularization (ET or open intervention), post-12 weeks (exercise and control groups), 6 months following intervention time period
Title
Change in peak oxygen uptake
Time Frame
Baseline, post-revascularization (ET or open intervention), post-12 weeks (exercise and control groups), 6 months following intervention time period
Title
Change in functional ability
Description
Functional ability will be assessed with the 6-min walk test and Short Physical Performance Battery which consists of 1) walking short distances, 2) completing balance tests and 3) sit and standing from a chair 5 times.
Time Frame
Baseline, post-revascularization (ET or open intervention), post-12 weeks (exercise and control groups), 6 months following intervention time period
Title
Evaluation of total volume of activity
Time Frame
post-12 weeks (exercise and control groups)
Title
Evaluation of exercise adherence
Description
For patients randomized to the exercise therapy group
Time Frame
post-12 weeks (exercise and control groups)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women diagnosed with atherosclerotic PAD ≥40 years of age An abnormal ankle-brachial index (ABI) of ≤.90 For patients with an ABI >.90 and <1.00, a post-exercise ABI drop of 15% or more compared to the resting ABI Patients receiving lower extremity ET or peripheral open intervention Patients not receiving lower extremity ET or peripheral open intervention but present with stable claudication and an abnormal ABI Exclusion Criteria: Lower extremity amputation(s), including a toe amputation, which interfere (s) with walking on the treadmill Individuals with critical limb ischemia defined by ischemic rest pain or ischemic ulcers/gangrene on the lower extremities PAD of non-atherosclerotic nature (e.g., fibromuscular dysplasia, irradiation, endofibrosis) Coronary artery bypass grafts or major surgical procedures within 6 months prior to screening Individuals whose walking exercise is primarily limited by symptoms of chronic obstructive pulmonary disease, angina, or heart failure Individuals who are unable to walk on the treadmill at a speed of at least 2 mph for at least 1 minute Individuals who have had a myocardial infarction within 3 months prior to screening Individuals who demonstrate symptoms consistent with acute coronary syndrome Individuals who exhibit ischemia as documented on the 12-lead electrocardiogram including horizontal or down-sloping ST-segment depression ≥0.5 mm at rest and >1 mm with exercise in 2 contiguous leads, relative to the PR-segment (ST-segment measured 0.08 seconds after the J point, ST-segment elevation ≥1 mm) Individuals who have had a transient ischemic attack or stroke 3 months prior to screening Individuals with left bundle branch block or sustained ventricular tachycardia (>30 sec) during screening Individuals with uncontrolled hypertension (≥180 systolic or ≥100 diastolic resting blood pressure) during screening Treatment with pentoxifylline or cilostazol for the treatment of claudication 4 weeks prior to screening; Patients can be reconsidered for study inclusion following a 1 month washout period from these medications Electrolyte abnormalities (e.g., potassium <3.3 mmol∙Lˉ1 ) Pregnancy, fertility without protection against pregnancy (for women of childbearing potential, a serum pregnancy test will be performed at screening) Incarcerated individuals Individuals acutely impaired by alcohol or other illicit drugs Poorly controlled diabetes defined as glycated hemoglobin >12% Severely anemic patients (Hgb <11 g∙dLˉ1 for women and <10 g∙dLˉ1 for men) For patients who have not received peripheral revascularization, an ABI of >0.90 For patients with equivocal resting ABIs (0.91-0.99), a drop of <15% in the post-exercise ABI For individuals with non-compressible vessels (ABI >1.39) who have a toe- brachial index (TBI) >0.70 Inability to speak English Other clinically significant disease that is, in the opinion of the study team, not stabilized or may otherwise confound the results of the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ryan J. Mays, PhD, MPH, MS
Organizational Affiliation
International Heart Institute of Montana Foundation
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Heart Institute of Montana Foundation
City
Missoula
State/Province
Montana
ZIP/Postal Code
59802
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.nhlbi.nih.gov/
Description
Click here for more information about the sponsor.
URL
http://www.nih.gov/
Description
Click here for more information about the sponsor.

Learn more about this trial

Community Walking Exercise for Patients With Peripheral Artery Disease

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