This trial is active, not recruiting.

Condition peripheral arterial disease
Treatment exercise
Sponsor Palo Alto Institute for Research and Education, Inc
Collaborator Stanford University
Start date September 2006
End date June 2016
Trial size 300 participants
Trial identifier NCT00537225, 5RO1NR9197-2


Patients with peripheral arterial disease (PAD) experience significant functional limitations due to ischemic symptoms (claudication) and are at high risk for CVD morbidity and mortality resulting from untreated cardiovascular disease (CVD) risk factors and aggressive atherosclerosis. The overall Goal of this randomized controlled clinical trial is to examine the synergistic effect of a multifactor risk reduction on walking distance, blood flow and quality of life in 300 patients with PAD.

Specifically, we will compare the effects of 24 months of a novel, yet well-tested multiple risk factor reduction program, the Health Education and Risk Reduction Training (HEAR2T) Program for PAD versus enhanced standard care on: 1) symptom limited walking distance as assessed by treadmill exercise testing and walking impairment questionnaire; 2) endothelial function as measured by flow mediated vasodilation (FMVD) via brachial artery ultrasound. We will also explore the association between FMVD and decreased oxidative stress (as measured by oxygen radical absorbance capacity and urinary isoprostanes) and reduced degradation of nitric oxide (NO) and/or increased NO biosynthesis (as measured by urine nitrogen oxide, plasma nitrogen oxide, plasma asymmetric dimethylarginine, plasma, urine and platelet cyclic GMP).

Secondary hypotheses examine the association between reducing CVD risk factors, improved endothelial function, increased walking distance, improved quality of life and number of metabolic syndrome abnormalities in PAD patients.

Significance. This study will contribute to evidence on the efficacy of multiple risk factor reduction on improving physical function and quality of life in the understudied, elderly PAD patient. This study will also provide preliminary evidence for the biological basis for the efficacy of multifactor risk reduction in restoring vascular homeostasis, critical because of its role in antiatherogenesis and maintaining vasoreactivity, both necessary for slowing the progression of atherosclerosis.

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Intervention model parallel assignment
Masking single blind (subject)
Primary purpose treatment
(Placebo Comparator)
enhanced usual care
tailored multifactor CVD risk reduction

Primary Outcomes

walking time
time frame: 24 months

Secondary Outcomes

quality of life, biomarkers of CVD risk, endothelial function
time frame: 24 months

Eligibility Criteria

Male or female participants from 50 years up to 90 years old.

Inclusion Criteria: Subjects eligible for this study include: 1. Age 50 years or older with one or more CVD risk factor 2. PAD secondary to atherosclerosis with significant claudication 3. Claudication is defined as pain, ache, cramp, numbness or severe fatigue of muscles of one or both lower extremities, reproducibly provoked by walking causing the patient to slow or stop walking pace 4. Ankle-brachial index (ABI) < 0.90 5. In diabetics ABI is inaccurate, in which case, we will substitute toe pressures < 60 mmHg 6. ABI one minute after exercise is at least 20% lower than index leg resting ABI 7. Capable of walking at least 50 feet 8. Primary limitation to walking is claudication, not coexisting conditions such as severe CAD, uncontrolled hypertension, pulmonary disease, severe arthritis, or orthopedic conditions 9. Difference of walking time between two consecutive (of four) baseline treadmill tests must be < 25%. Exclusion Criteria: Exclusion criteria include: 1. Active malignancy or tumor or other condition that would severely limit life expectancy 2. Any type of major surgery during the last 3 months (i.e. aortic or lower extremity arterial surgery, angioplasty, or lumbar sympathectomy, leg amputation above the ankle) 3. Residence in a long-term institutional setting 4. Psychiatric disorders with currently active manifestations 5. Uncontrolled metabolic disorders (renal failure, liver failure, thyrotoxicosis) 6. Active symptoms suggestive of an acute coronary syndrome or decompensated heart failure 7. Lack of phone access (either by self or through neighbors/family members) 8. Other specified circumstances incompatible with case-management (i.e., plan to move away from area) 9. Presence of another household member or first-degree relative already enrolled in the study 10. Current enrollment in another clinical trial 11. Regular participation in an exercise program for at least 3 months prior to study entry.

Additional Information

Official title Multifactor Risk Reduction for Optimal Management of PAD
Principal investigator Roberta K Oka, ANP, DNSc
Description in progress
Trial information was received from ClinicalTrials.gov and was last updated in October 2014.
Information provided to ClinicalTrials.gov by Palo Alto Institute for Research and Education, Inc.