The Effects of a Novel, Non-ischemic and Pain-free Exercise Intervention in Peripheral Artery Disease

Last updated: June 11, 2025
Sponsor: University of Oklahoma
Overall Status: Active - Recruiting

Phase

N/A

Condition

Intermittent Claudication

Thrombosis

Peripheral Arterial Occlusive Disease

Treatment

Exercise

Clinical Study ID

NCT05712395
16294
R01AG071778-01A1
  • Ages > 60
  • All Genders

Study Summary

This study is a 3-month, prospective, randomized controlled clinical trial designed to address the efficacy of the Non-Ischemic Exercise (NICE) program to improve exercise and vascular outcome measures in patients with peripheral artery disease (PAD).

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. history of claudication assessed by the Walking Impairment Questionnaire,

  2. ambulatory leg pain in either one or both legs consistent with intermittentclaudication confirmed during a screening graded treadmill test using theGardner-Skinner protocol,

  3. an ABI <= 0.90 at rest or > 20% decrease in ankle systolic blood pressure in eitherone or both legs immediately following the treadmill exercise test.

  4. age >= 60 years.

Exclusion

Exclusion Criteria:

  1. absence of PAD (ABI > 0.90 at rest and ankle systolic blood pressure < 20% decreaseafter exercise,

  2. inability to obtain an ABI measure due to non-compressible vessels (ABI > 1.40),

  3. asymptomatic PAD (Fontaine Stage I) determined from the medical history and verifiedduring the graded treadmill test,

  4. rest pain due to PAD (Fontaine stage III)

  5. tissue loss due to PAD (Fontaine stage IV)

  6. use of medications indicated for the treatment of intermittent claudication (cilostazol and pentoxifylline) initiated within three months prior toinvestigation,

  7. peripheral revascularization within one month prior to investigation, or peripheralrevascularization performed during the study,

  8. exercise tolerance limited by any disease process other than PAD,

  9. active cancer,

  10. kidney failure defined as stage 5 chronic kidney disease,

  11. a calf skin fold measurement > 25 mm, because of potential interference with thelight path of the NIRS probe from penetrating the subcutaneous tissue,

  12. pulse arterial oxygen saturation of the index finger < 95% because of potentialdeleterious effect on calf muscle StO2 from poor pulmonary gas exchange, and

  13. failure to complete the baseline run-in phase within three weeks.

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: Exercise
Phase:
Study Start date:
September 09, 2024
Estimated Completion Date:
July 31, 2029

Study Description

Specific Aims. The investigator proposes to test our central hypothesis that the NICE intervention performed without inducing leg ischemia and its' damaging sequela will be a superior exercise paradigm to increase peak walking time and HRQoL more than the Standard ischemic and painful exercise paradigm via greater improvement in microvascular mechanisms. This clinically relevant hypothesis will be tested through the following aims:

Aim 1 (Exercise Outcomes) To compare the changes in ambulation and HRQoL in PAD patients randomized to either the NICE slow walking program or to the Standard program of ischemic and painful exercise.

Aim 2a (Vascular Outcomes) To compare the changes in local microvascular function of the lower extremities, inflammation and oxidative stress in patients following the NICE program, and following the Standard ischemic and painful program.

Aim 2b (Exploratory Aim) To explore whether the changes in local microvascular function and systemic vascular biomarkers are associated with the changes in peak walking time following the NICE and Standard programs, and whether the association is stronger following the NICE program.

Methods. This is a 3-month, patient-oriented, translational, comparative effectiveness randomized controlled trial. One-hundred patients will be randomized into either the NICE program (N=50) or the Standard exercise program (N=50). All patients will perform supervised treadmill walking for 3 months. Patients randomized to the NICE program will walk intermittently at a slow speed of approximately 1.4 mph for only 2-3 minute bouts that do not elicit claudication pain. Patients randomized to the Standard program will walk intermittently at a speed of approximately two mph to near maximal claudication pain.

Connect with a study center

  • O'Donoghue Research Building, University of Oklahoma Health Sciences Center

    Oklahoma City, Oklahoma 73117
    United States

    Active - Recruiting

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