4.6 Article

Study Design, Rationale, and Methodology for Promote Weight Loss in Patients With Peripheral Artery Disease Who Also Have Obesity: The PROVE Trial

Journal

JOURNAL OF THE AMERICAN HEART ASSOCIATION
Volume 12, Issue 17, Pages -

Publisher

WILEY
DOI: 10.1161/JAHA.123.031182

Keywords

eating behavior; home-based exercise; mitochondria; obesity; peripheral artery disease; physical function; randomized controlled trial

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This study aims to evaluate the effects of exercise with an intervention of coaching and a smartphone application on walking performance in people with peripheral artery disease (PAD) and overweight/obesity, compared with exercise alone. The results will provide treatment guidelines for patients with PAD and overweight/obesity.
BACKGROUND: Overweight and obesity are associated with adverse functional outcomes in people with peripheral artery disease (PAD). The effects of weight loss in people with overweight/obesity and PAD are unknown. METHODS: The PROVE (Promote Weight Loss in Obese PAD Patients to Prevent Mobility Loss) Trial is a multicentered randomized clinical trial with the primary aim of testing whether a behavioral intervention designed to help participants with PAD lose weight and walk for exercise improves 6-minute walk distance at 12-month follow-up, compared with walking exercise alone. A total of 212 participants with PAD and body mass index >= 25 kg/m(2) will be randomized. Interventions are delivered using a Group Mediated Cognitive Behavioral intervention model, a smartphone application, and individual telephone coaching. The primary outcome is 12-month change in 6-minute walk distance. Secondary outcomes include total minutes of walking exercise/wk at 12-month follow-up and 12-month change in accelerometer-measured physical activity, the Walking Impairment Questionnaire distance score, and the Patient-Reported Outcomes Measurement Information System mobility questionnaire. Tertiary outcomes include 12-month changes in perceived exertional effort at the end of the 6-minute walk, diet quality, and the Short Physical Performance Battery. Exploratory outcomes include changes in gastrocnemius muscle biopsy measures of mitochondrial cytochrome C oxidase activity, mitochondrial biogenesis, capillary density, and inflammatory markers. CONCLUSIONS: The PROVE randomized clinical trial will evaluate the effects of exercise with an intervention of coaching and a smartphone application designed to achieve weight loss, compared with exercise alone, on walking performance in people with PAD and overweight/obesity. Results will inform optimal treatment for the growing number of patients with PAD who have overweight/obesity. REGISTRATION: URL: https://www.clinicaltrials.gov; Unique identifier: NCT04228978.

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