Clinical Trials Directory

Trials / Completed

CompletedNCT04330560

Exercise-based Telerehabilitation in the Cardiac Rehabilitation Program

Feasibility and Preliminary Evaluation and the Effects of Exercise-based Telerehabilitation on the Acceptability and Safety, and Clinical Effectiveness Among Patients With Coronary Heart Disease Undergoing the Cardiac Rehabilitation Program

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
University of Malaya · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The intervention will involve a system that comprises a wrist-worn activity tracker and a smartphone app that acts as a medium to link to the healthcare website

Detailed description

Feasibility study objective: - To investigate the feasibility and preliminary of exercise-based telerehabilitation before undertaking full-scale RCT. Randomized control trial objective: - 1. Primary Objective: To determine the exercise capacity among patients with CHD, 2. Secondary Objectives: To assess patient exercise adherence and determine the changes in other clinical health outcomes. Study Population: Patients with coronary heart disease Description of Sites/Facilities Enrolling Participants: Patient engagement with the cardiac rehabilitation phase 2 (CRP2) at the University Malaya Medical Centre (UMMC). Description of Study Intervention: This study is a mixed-methods study consisting of a quantitative study (feasibility, preliminary evaluation, and full randomized control trial) and a qualitative study (interviewing). The present study will be conducting a single-blinded, three-arm, parallel over a 12-weeks study period during CRP2. Measurement will be collected during pre-and post-test.

Conditions

Interventions

TypeNameDescription
DEVICEExercise telemonitoring connects to healthcare platformThe participant is required to wear the fitness tracker every day during waking hours throughout the 12 weeks of intervention (except during sleeping, bathing, and swimming) link to the healthcare practitioner
DEVICEExercise self-monitoringThe participant is required to wear the fitness tracker every day during waking hours throughout the 12 weeks of intervention (except during sleeping, bathing, and swimming) for exercise self-monitoring.
DEVICEExercise teleconsultationConducted through smartphone video call app.
PROCEDUREOther CR componentsIncluding dietary, psychology, education conducted at the center.
PROCEDUREStandard careUndergoing standard care by cardiac rehabilitation at the center

Timeline

Start date
2020-12-01
Primary completion
2021-05-26
Completion
2023-12-31
First posted
2020-04-01
Last updated
2024-05-08

Locations

1 site across 1 country: Malaysia

Source: ClinicalTrials.gov record NCT04330560. Inclusion in this directory is not an endorsement.