Evaluation of a personalized home-based exercise program for patients with combined chronic cardiac and pulmonary disease: a feasibility study

Completed

• Conditions: 10006436; combination of different chronic pulmonary and cardiac diseases; not applicable; 10019280

• Registration Number: NL-OMON46005
• Lead Sponsor: Maxima Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 10

Inclusion Criteria

1. Patients with combined chronic pulmonary and cardiac disease already participating in remote patient care.
2. Motivated to participate in an exercise program.
3. Age * 18 years.
4. Speaking, writing and reading the Dutch language.

Exclusion Criteria

1. Neurological, orthopaedic of peripheral vascular conditions preventing the patient from performing exercise.
2. Hemodynamic significant valvular disease.
3. Proven cardiac ischemia or heart rhythm disturbances at a low-intensity exercise level.
4. Already participating in the IN-TOuCH trial (telemonitoring for patients with COPD and chronic heart failure)
5. Already receiving physio- and/or occupational therapy.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary endpoint is feasibility of a home-based exercise program (i.e. the<br /><br>ability to complete the exercise program and a qualitative exploration of<br /><br>barriers for adherence). </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Secondary endpoints include patient satisfaction, functional capacity and<br /><br>quality of life. </p><br>