Effect of a Home-Based, Walking Exercise Behavior Change Intervention vs Usual Care on Walking in Adults With Peripheral Artery Disease

医学 物理疗法 随机对照试验 心理干预 干预(咨询) 间歇性跛行 物理医学与康复 动脉疾病 血管疾病 内科学 精神科
作者
Lindsay Bearne,Brittannia Volkmer,Janet L. Peacock,Mandeep Sekhon,Graham Fisher,Melissa Galea Holmes,Abdel Douiri,Aliya Amirova,Dina Farran,Sophia Quirke-McFarlane,Bijan Modarai,Catherine Sackley,John Weinman,Julie Bieles,David P. French,Esther Williamson,Catherine Minns- Lowe,Nicholas T. Longford,Sanjay Patel,P. J. Holt,Abdullah Jiwabi,Sharlene Greenwood,Janice Tsui,Paritosh Sharma,Helen Creasy,Heather Waring,Joanne Barnes,Jonathan da Costa,Bethany Hedges,Emma Bowen,Stuart Brandom,Leon Palmer Wilson,Heather Pursey,Diana Ascenso,Ellen M. Castle,Juliet Mayes,Ellie Lyons,Francesca Gowing,Joanna Buckley,Peter May
出处
期刊:JAMA [American Medical Association]
卷期号:327 (14): 1344-1344 被引量:23
标识
DOI:10.1001/jama.2022.3391
摘要

Importance

Home-based walking exercise interventions are recommended for people with peripheral artery disease (PAD), but evidence of their efficacy has been mixed.

Objective

To investigate the effect of a home-based, walking exercise behavior change intervention delivered by physical therapists in adults with PAD and intermittent claudication compared with usual care.

Design, Setting, and Participants

Multicenter randomized clinical trial including 190 adults with PAD and intermittent claudication in 6 hospitals in the United Kingdom between January 2018 and March 2020; final follow-up was September 8, 2020.

Interventions

Participants were randomized to receive a walking exercise behavior change intervention delivered by physical therapists trained to use a motivational approach (n = 95) or usual care (n = 95).

Main Outcomes and Measures

The primary outcome was 6-minute walking distance at 3-month follow-up (minimal clinically important difference, 8-20 m). There were 8 secondary outcomes, 3 of which were the Walking Estimated Limitation Calculated by History (WELCH) questionnaire (score range, 0 [best performance] to 100), the Brief Illness Perceptions Questionnaire (score range, 0 to 80 [80 indicates negative perception of illness]), and the Theory of Planned Behavior Questionnaire (score range, 3 to 21 [21 indicates best attitude, subjective norms, perceived behavioral control, or intentions]); a minimal clinically important difference was not defined for these instruments.

Results

Among 190 randomized participants (mean age 68 years, 30% women, 79% White race, mean baseline 6-minute walking distance, 361.0 m), 148 (78%) completed 3-month follow-up. The 6-minute walking distance changed from 352.9 m at baseline to 380.6 m at 3 months in the intervention group and from 369.8 m to 372.1 m in the usual care group (adjusted mean between-group difference, 16.7 m [95% CI, 4.2 m to 29.2 m];P = .009). Of the 8 secondary outcomes, 5 were not statistically significant. At 6-month follow-up, baseline WELCH scores changed from 18.0 to 27.8 in the intervention group and from 20.7 to 20.7 in the usual care group (adjusted mean between-group difference, 7.4 [95% CI, 2.5 to 12.3];P = .003), scores on the Brief Illness Perceptions Questionnaire changed from 45.7 to 38.9 in the intervention group and from 44.0 to 45.8 in the usual care group (adjusted mean between-group difference, −6.6 [95% CI, −9.9 to −3.4];P < .001), and scores on the attitude component of the Theory of Planned Behavior Questionnaire changed from 14.7 to 15.4 in the intervention group and from 14.6 to 13.9 in the usual care group (adjusted mean between-group difference, 1.4 [95% CI, 0.3 to 2.5];P = .02). Thirteen serious adverse events occurred in the intervention group, compared with 3 in the usual care group. All were determined to be unrelated or unlikely to be related to the study.

Conclusions and Relevance

Among adults with PAD and intermittent claudication, a home-based, walking exercise behavior change intervention, compared with usual care, resulted in improved walking distance at 3 months. Further research is needed to determine the durability of these findings.

Trial Registrations

ISRCTN Identifier:14501418; ClinicalTrials.gov Identifier:NCT03238222
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