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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON46005
Enrollment
10
Registered
2018-11-06
Start date
2019-10-29
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

combination of different chronic pulmonary and cardiac diseases not applicable

Interventions

Patients included will receive a two-month home-based exercise program and are coached by a physiotherapist and/or ergo therapist via video calls. The content of this exercise program will be based

Sponsors

Maxima Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
The primary endpoint is feasibility of a home-based exercise program (i.e. the ability to complete the exercise program and a qualitative exploration of barriers for adherence).

Secondary

MeasureTime frame
Secondary endpoints include patient satisfaction, functional capacity and quality of life.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)