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Home-based Mobile Guided Exercise-based Cardiac Rehabilitation Among Patients Undergoing TAVR — REHAB-TAVR  

Cardiac Rehabilitation Clinical Trial

Official title:
A Home-based Mobile Guided Exercise-based Cardiac Rehabilitation Among Patients Undergoing Transcatheter Aortic Valve Replacement (REHAB-TAVR): a Randomized Clinical Trial

Clinical Trial Summary

A two-parallel, evaluator-blind, single-center, randomized controlled trial was designed to assess the effectiveness of a home-based mobile guided exercise-based cardiac rehabilitation among patients undergoing Transcatheter Aortic Valve Replacement.

Clinical Trial Description

The purpose of our study was to investigate the effect of home-based mobile-guided exercise-based cardiac rehabilitation on the improvement of exercise capacity among patients undergoing transcatheter aortic valve replacement. 90 subjects will be recruited and followed up for a six-minute walk distance, short physical performance battery, exercise adherence, quality of life, frailty, nutritional status, sleep status, readmission rate, and all-cause mortality et al. The subjects will be invited to participate in on-site visits at 1, 3, and 6 months. Patients in the interventional group will receive a home-based mobile-guided exercise-based cardiac rehabilitation for 3 months. The home-based mobile-guided exercise-based cardiac rehabilitation is a multi-component intervention strategy including the preparation for discharge, family support, motivational interviews, health education, telephone follow-up, wearable devices, APP, et al. While the patients in the control group will receive routine care. For example, the preparation for discharge of the control group does not include the guidance of mobile-guided exercise-based cardiac rehabilitation, family support, and motivational interviews. After discharge, nurses will conduct telephone follow-ups once a month for the control group. Baseline data and outcomes will be collected in a Case Report Form. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05989594
Study type Interventional
Source Shanghai Zhongshan Hospital
Contact Zhiyun Shen
Phone +8318317089276
Email Shen.zhiyun@zs-hospital.sh.cn
Status Not yet recruiting
Phase N/A
Start date September 1, 2023
Completion date June 30, 2024
View Details
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