Rehabilitation through exercise prescription for cardiac patients using an artificial intelligence-based programme - RECAP

Not Applicable

• Conditions: Service users requiring cardiac rehabilitation; Not Applicable

• Registration Number: ISRCTN97352737
• Lead Sponsor: South Tees Hospitals NHS Foundation Trust

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-11-17
• Last Update Posted: 9 January 2023
• Study Completion: 2024-03-15

Recruitment & Eligibility

• Status: Ongoing
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Patients eligible for cardiac rehabilitation

Exclusion Criteria

1. Awaiting urgent surgery
2. Unstable angina
3. Pregnancy
4. Currently enrolled in another interventional clinical trial or experiment
5. Malignant arrhythmias
6. Contraindications to rehabilitation - e.g.
6.1. Severe musculoskeletal conditions affecting exercise ability
6.2. Acute systemic illness or fever
6.3. Acute pericarditis or myocarditis
6.4. Uncontrolled atrial or ventricular arrhythmias
6.5. Uncontrolled sinus tachycardia
6.6. Aortic stenosis associated with pre-syncope/syncope
6.7. Uncompensated Heart failure
6.8. Complete atrioventricular block without a pacemaker
6.9. Recent embolism

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Feasibility of conducting a large-scale randomised controlled trial measured using participant recruitment and dropout rates, acceptability of the intervention and the feasibility of randomisation at 12 weeks

Secondary Outcome Measures

Name	Time	Method
<br> 1. Aerobic capacity and endurance measured using the 6-minute walk test at baseline and 8 weeks<br> 2. Health-related quality of life measured using EQ-5D-5L questionnaire at baseline and 8 weeks<br> 3. Health-related quality of life measured using SF-36 questionnaire at baseline and 8 weeks<br> 4. Anxiety and depression assessed using HADS questionnaire at baseline and 8 weeks<br> 5. Impact on quality of life measured using PROM-CR questionnaire at 8 weeks<br> 6. Performance in activities of daily living measured using Barthel Index questionnaire at baseline and 8 weeks<br> 7. Adherence to the intervention, including usage of the app measured using app s at 8 weeks<br>