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The feasibility of a home-based remotely supervised maintenance exercise training program in patients with COPD

The feasibility of a home-based remotely supervised maintenance exercise training program in patients with COPD - The feasibility of a home-based maintenance exercise program in COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON51560
Enrollment
10
Registered
2022-08-18
Start date
2024-01-29
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Chronic bronchitis, pulmonary emphysema

Interventions

Bicycle with remote supervision

Sponsors

CIRO
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Confirmed diagnoses of COPD. - Clinical stable as assessed by the chest physician. - Participation in cycle training during pulmonary rehabilitation. - No balance problems as assessed by the Tinetti test during the intake with the physiotherapist in the routine baseline assessment (score >= 24). - Internet (Wi-Fi) access at home. - Provision of informed consent prior to any study specific procedures. - Complete data on study endpoints (i.e. constant work rate cycle test, six-minute walk test, COPD Assessment Test, Hospital Anxiety and Depression Scale).

Exclusion criteria

Exclusion criteria: - Lack of motivation for voluntary participation in the study. - Insufficient ability to read, write or understand the Dutch language. - Incapability to follow study procedures (including but not limited to participate in the exercise training program or follow instructions of the research team).

Design outcomes

Primary

MeasureTime frame
- Feasibility will be assessed by the adherence to home-based maintenance exercise training sessions (i.e. the number of completed training sessions uploaded in the web-portal and training variables of these sessions (duration, intensity)). - Safety will be assessed by the number of (S)AEs. - Efficacy will be assessed by the change in exercise capacity on constant work rate cycle test (endurance time, Borg scores for dyspnea and fatigue).

Secondary

MeasureTime frame
- To explore changes in functional exercise capacity assessed on 6 minute walk test. - To explore changes on patient-reported outcomes using COPD Assessment Test and Hospital Anxiety and Depression Scale. - To explore patient satisfaction using a structured interview and the Quebec User Evaluation of Satisfaction with Assistive Technology (QUEST).

Countries

Netherlands

Contacts

Public ContactA.W. Vaes

CIRO

anoukvaes@ciro-horn.nl0475587602

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Feb 7, 2026