Construction and Application Plan of Home Cardiac Rehabilitation for Patients Undergoing TAVR

Launched by SECOND AFFILIATED HOSPITAL, SCHOOL OF MEDICINE, ZHEJIANG UNIVERSITY · May 13, 2024

Keywords

ClinConnect Summary

This clinical trial is exploring a new home-based cardiac rehabilitation program specifically designed for patients who have recently undergone Transcatheter Aortic Valve Replacement (TAVR) surgery. The aim is to help these patients follow their rehabilitation plan more closely using mobile technology. The researchers believe that by focusing on patients’ abilities, opportunities, and motivations, they can create a program that fits their needs and encourages better participation in their recovery process.

To participate in this study, individuals must be recent TAVR patients who are classified as having mild to moderate heart symptoms. They should be comfortable using mobile devices like smartphones and be willing to engage in a digital rehabilitation program. Unfortunately, patients with certain serious health issues, significant hearing or vision impairments, or cognitive challenges are not eligible. Those who join can expect support from a management system that provides real-time guidance and information to help them on their path to recovery at home.

Gender

ALL

Eligibility criteria

• • Inclusion Criteria: Patients undergoing TAVR who were classified as Grade I-III by the New York Heart Association (NYHA); Patients are able to use mobile devices such as smartphones; Patients who have obtained admission qualifications after undergoing digital home cardiac rehabilitation risk assessment by the rehabilitation team; The patient and their family members voluntarily participate in this study and are willing to provide an informed consent form; Able to use remote rehabilitation diagnosis and treatment systems Exclusion Criteria: Malignant tumors or those with serious complications; Patients with hearing and visual impairments; Patients with limited physical activity due to other diseases; Patients with obvious cognitive or mental disorders; Patients without Internet connection after returning home from hospital; Patients who have participated in or participated in other trials or rehabilitation plans within the past three months.

Trial Officials