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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03845036
Other study ID # 16383
Secondary ID R01AG070086-01A1
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 3, 2024
Est. completion date May 31, 2027

Study information

Verified date February 2024
Source University of Oklahoma
Contact Andrew Gardner, Ph.D.
Phone 405-271-4742
Email andrew-gardner@ouhsc.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is a 3-month, prospective, randomized controlled clinical trial designed to address the efficacy of the DASH dietary program combined with a home-based exercise program, quantified by a step activity monitor, to improve exercise and vascular outcome measures in patients with PAD.


Description:

This study seeks to (1) compare the changes in 6-minute walk distance (6MWD) and physical function quality of life in patients with peripheral artery disease (PAD) following a combined intervention of the dietary approaches to stop hypertension (DASH) dietary program plus a home-based exercise program, and following a home-based exercise program alone; and (2) compare the changes in microvascular function and inflammation in patients following the combined DASH diet and home-based exercise program, and the home-based exercise program alone. The investigators hypothesize that the combined DASH diet and exercise program will result in greater increases in 6MWD and in the physical function quality of life than the exercise program alone. Further, it is hypothesized that the combined DASH diet and exercise program will result in greater improvements in calf muscle oxygen saturation [StO2] following exercise, and in high-sensitivity C-reactive protein (hsCRP]) than the exercise program alone. The home-based exercise program consists of intermittent walking to moderate claudication pain in a home-based setting. The DASH dietary program consists of the dietary approaches to stop hypertension diet emphasizing foods rich in fruits, vegetables, whole grains, and low-fat dairy.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 150
Est. completion date May 31, 2027
Est. primary completion date May 31, 2027
Accepts healthy volunteers No
Gender All
Age group 60 Years and older
Eligibility Inclusion Criteria: 1. History of claudication, 2. Presence of PAD, defined by meeting at least one of the following criteria (ABI at rest < 0.90, or > 20% decrease in ABI following a heel-rise exercise test in patients with a normal ABI at rest (> 0.90), or history of peripheral revascularization. Exclusion Criteria: 1. absence of PAD, defined by meeting all of the following 3 criteria (ABI at rest > 0.90), < 20% decrease in ABI following a heel-rise exercise test, and no history of peripheral revascularization, 2. non-compressible vessels (ABI > 1.40), 3. rest pain due to PAD (Fontaine stage III; Rutherford Grade II), 4. tissue loss due to PAD (Fontaine stage IV; Rutherford Grade III), 5. use of medications indicated for the treatment of intermittent claudication (cilostazol and pentoxifylline) initiated within three months prior to investigation, 6. peripheral revascularization within one month prior to investigation, 7. active cancer, 8. end stage renal disease defined as stage 5 chronic kidney disease, 9. medical conditions that are contraindicative for exercise according to the American College of Sports Medicine, 10. cognitive dysfunction (mini-mental state examination score < 24), and 11. failure to complete the baseline tests within three weeks.

Study Design


Intervention

Behavioral:
DASH Diet plus Home-Based Exercise
The DASH dietary program consists of a diet emphasizing foods rich in fruits, vegetables, whole grains, and low-fat dairy, in which patients record daily servings of fruits and vegetables. The home-based exercise program consists of intermittent walking to moderate claudication pain 3 times per week for 3 months in a home-based setting.
Home-Based Exercise
The home-based exercise program consists of intermittent walking to moderate claudication pain 3 times per week for 3 months in a home-based setting.

Locations

Country Name City State
United States O'Donoghue Research Building, University of Oklahoma Health Sciences Center Oklahoma City Oklahoma

Sponsors (4)

Lead Sponsor Collaborator
University of Oklahoma Case Western Reserve University, Milton S. Hershey Medical Center, National Institute on Aging (NIA)

Country where clinical trial is conducted

United States, 

References & Publications (3)

Gardner AW, Bright BC, Ort KA, Montgomery PS. Dietary intake of participants with peripheral artery disease and claudication. Angiology. 2011 Apr;62(3):270-5. doi: 10.1177/0003319710384395. — View Citation

Gardner AW, Parker DE, Montgomery PS, Blevins SM. Step-monitored home exercise improves ambulation, vascular function, and inflammation in symptomatic patients with peripheral artery disease: a randomized controlled trial. J Am Heart Assoc. 2014 Sep 18;3( — View Citation

Gardner AW, Parker DE, Montgomery PS, Scott KJ, Blevins SM. Efficacy of quantified home-based exercise and supervised exercise in patients with intermittent claudication: a randomized controlled trial. Circulation. 2011 Feb 8;123(5):491-8. doi: 10.1161/CI — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Peak Walking Time The change in the time walked on a treadmill test 3 months
Primary Physical Function subscale of quality of life from the Medical Outcomes Study Short-Form 36 questionnaire The change in the Physical Function subscale from the pre-test value to the post-test value 3 months
Secondary calf muscle oxygen saturation The change in the calf muscle oxygen saturation value during exercise from the pre-test value to the post-test value 3 months
Secondary 6-minute walk distance The change in 6-minute walk distance from the pre-test value to the post-test value 3 months
Secondary high-sensitivity C-reactive protein The change in the high-sensitivity C-reactive protein value from the pre-test value to the post-test value 3 months
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