Protein and Exercise to Reverse Frailty in Older Men and Women Undergoing Transcatheter Aortic Valve Replacement: Design of the PERFORM-TAVR Trial

医学 阀门更换 生活质量(医疗保健) 临床试验 临床终点 内科学 随机对照试验 物理疗法 狭窄 护理部
作者
Rosie Fountotos,Sandra Lauck,Nicolò Piazza,Giuseppe Martucci,Rakesh C. Arora,Anita Asgar,Jessica Forcillo,Rémi Kouz,Marino Labinaz,André Lamy,Mark D. Peterson,Harindra C. Wijeysundera,L. Massé,Marie‐Claude Ouimet,Jopie Polderman,John G. Webb,Jonathan Afilalo
出处
期刊:Canadian Journal of Cardiology [Elsevier BV]
卷期号:40 (2): 267-274 被引量:12
标识
DOI:10.1016/j.cjca.2023.11.037
摘要

Abstract

Despite the high procedural success of transcatheter aortic valve replacement (TAVR), 2 out of 5 older adults report poor physical performance and health-related quality of life (HRQOL) in the ensuing months, particularly those with frailty. There has yet to be a trial examining the synergistic effects of exercise and protein supplementation to counteract frailty and improve patient-centred outcomes following TAVR. The PERFORM-TAVR trial is a multicentre parallel-group randomised clinical trial that is enrolling 200 frail older adults ≥ 70 years of age undergoing TAVR. Patients will be randomly allocated to 1 of 2 treatment groups: standard-of-care lifestyle education (control group) or protein-rich oral nutritional supplement for 4 weeks before TAVR with the addition of home-based supervised exercise sessions for 12 weeks after TAVR (intervention group). The primary outcome will be physical performance as measured by a blinded observer using the Short Physical Performance Battery at 3 months. Secondary outcomes at 3, 6, and 12 months will include HRQOL, as measured by the Short-Form 36 Physical and Mental Component summary scores, and a composite safety end point. The PERFORM-TAVR trial is testing a novel frailty intervention in older adults undergoing TAVR to optimise recovery and downstream HRQOL. This represents a potential paradigm shift that highlights the value of assessing and treating patients' frailty in parallel with their underlying heart valve disease.

Clinical Trial Registration

URL: https://www.clinicaltrials.gov. Unique identifier: NCT03522454.
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