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N/A N=305 Randomized Single-blind Treatment

Low InTensity Exercise Intervention in PAD

Peripheral Artery Disease

Enrolled (actual)
305
Serious AEs
33.4%
Results posted
Nov 2021
Primary outcome: Primary: Six-minute Walk Distance — -6.4; 34.5; -15.1 meters

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Exercise (Behavioral); Attention control (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Northwestern University
Primary completion
Oct 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Six-minute Walk Distance
SECONDARY
Six-minute Walk Distance
SECONDARY
Maximal Treadmill Walking Time
SECONDARY
Physical Activity Levels
SECONDARY
Walking Impairment Questionnaire (WIQ) Distance and Speed Score.
SECONDARY
Health-related Quality of Life Measure
SECONDARY
Adherence to Intervention
SECONDARY
Change in Muscle Biopsy Measures of Mitochondrial Oxidative Metabolism and Oxidative Stress.

Summary

This proposed study will determine whether a home-based exercise intervention that avoids continuous supervision and exercise-related ischemic pain improves walking performance at 52-week follow-up in people with PAD, compared to an attention control group and compared to a high intensity exercise intervention. In our secondary aims, we will determine whether high intensity exercise improves six-minute walk distance as compared to the attention control group. In secondary aims, we will also determine whether low intensity exercise and high intensity home-based exercise, respectively, improve patient reported outcomes, physical activity, and treadmill walking performance compared to attention control. Our intervention directly addresses two aspects of current practice guidelines that are major barriers to exercise for patients with PAD: 1) the recommendation for supervised exercise and 2) the recommendation for high intensity ischemic-pain inducing walking exercise.

Eligibility Criteria

Inclusion Criteria

All participants will have PAD. PAD will be defined as follows. First, an ABI 0.90 and 0.90 who have vascular lab evidence of PAD or angiographic evidence of PAD who have ischemic symptoms during the six-minute walk and/or treadmill exercise stress test will be eligible. In addition to meeting a criterion for PAD, all participants must be symptomatic, defined by one of the following criteria:; a) ischemic leg symptoms (primarily assessed with the San Diego Claudication Questionnaire); b) report ischemic leg symptoms at the end of the six-minute walk; c) report ischemic leg symptoms at the end of the baseline treadmill stress test; d) walking impairment questionnaire results, e) interview with the potential participant about the presence and nature of leg symptoms during walking activity.

Exclusion Criteria

  • Above or below knee amputation, critical limb ischemia, wheelchair confinement, or foot ulcer.
  • Individuals whose walking is limited by a condition other than PAD.
  • > Class II NYHA heart failure or angina. Increase in angina, angina at rest, or abnormal baseline treadmill stress test.
  • Major surgery including lower extremity revascularization or orthopedic surgery during the prior three months or anticipated in the next twelve months.
  • Major medical illness including renal disease requiring dialysis, lung disease requiring oxygen other than at night, or cancer (other than non-melanoma skin cancer) requiring treatment in the prior three years. Potential participants may still qualify if they have had treatment for early stage cancer in the previous three years and the prognosis is excellent.
  • Mini-mental status examination score <23, dementia, or psychiatric illness including severe depression or anxiety. Investigator discretion may be used to allow some people with an MMSE below 23 to participate if the investigator determines there is another reason for their lower score, including lack of sufficient familiarity with the English language or lack of sufficient education to achieve a score of 23 or higher.
  • Currently walking regularly for exercise at a level comparable to the amount of exercise prescribed in the intervention.
  • Current or recent (within 3 months) participation in another clinical trial or cardiac rehabilitation. For a clinical trial of a stem cell or gene therapy intervention, potential participants will be potentially eligible immediately after the final study visit for the clinical trial, so long as long as at least six months has passed since the participant received their final treatment in the stem cell or gene therapy intervention. For a clinical trial involving open-label therapy in which the treatment is not related to functional performance and will not change during the LITE Trial, participants may still qualify for the LITE Trial based on investigator discretion.
  • Individuals with PAD who have a history of lower extremity revascularization and have a normal ABI.
  • Individuals who are not able to walk for exercise at a sufficiently slow pace to avoid ischemic leg symptoms.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02538900). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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