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Effect of a home-based, walking exercise behavior change intervention versus usual care on walking in adults with peripheral artery disease: the MOSAIC randomized clinical trial [with consumer summary]
Bearne LM, Volkmer B, Peacock J, Sekhon M, Fisher G, Galea Holmes MN, Douiri A, Amirova A, Farran D, Quirke-McFarlane S, Modarai B, Sackley C, Weinman J, Bieles J, for the MOSAIC Trial Collaboration
JAMA 2022 Apr 12;327(14):1344-1355
clinical trial
7/10 [Eligibility criteria: Yes; Random allocation: Yes; Concealed allocation: No; Baseline comparability: Yes; Blind subjects: No; Blind therapists: No; Blind assessors: Yes; Adequate follow-up: Yes; Intention-to-treat analysis: Yes; Between-group comparisons: Yes; Point estimates and variability: Yes. Note: Eligibility criteria item does not contribute to total score] *This score has been confirmed*

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 to 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 metres at baseline to 380.6 metres at 3 months in the intervention group and from 369.8 metres to 372.1 metres in the usual care group (adjusted mean between-group difference, 16.7 metres (95% CI 4.2 metres to 29.2 metres); p = 0.009). 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 = 0.003), 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 < 0.001), 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 = 0.02). 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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