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INSPIRE

Influencing self-management during pulmonary rehabilitation to empower patients - INSPIRE: Influencing Self-management during Pulmonary Rehabilitation to Empower Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON61362
Enrollment
40
Registered
2026-01-13
Start date
2026-10-01
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Chronic Obstructive Pulmonary Disease COPD

Interventions

The intervention consists of using an online program that supports guidance provided by a physical therapist or exercise therapist. The program is accessible via a smartphone or tablet and includes in

Sponsors

Hogeschool van Amsterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: In order to be eligible to participate in this study, a participant must meet all of the following criteria:Age = 45 years.Have a diagnosis of COPD GOLD stage 2–3 and be referred for pulmonary rehabilitation in primary care.

Exclusion criteria

Exclusion criteria: A potential participant who meets any of the following criteria will be excluded from participation in this study:Patients who are referred for rehabilitation in a secondary or tertiary centerInability to fill out the questionnaires due to digital literacy or language. Serious disease interfering with participation in the study such as orthopaedic or neurological conditions impeding physical activity. 

Design outcomes

Primary

MeasureTime frame
The primary objective of  this study is to determine the feasibility of the INSPIRE intervention (e.g. acceptability, integration and usability among others) in physical therapists and patients with COPD. 

Secondary

MeasureTime frame
The secondary objective of this study is to evaluate changes in physical capacity, self-management behavior, disease burden, dyspnea and fear of movement in patients with COPD pre-and post-intervention. In addition, changes in physical capacity and disease burden (which are measured as part of usual care) will be compared to a historical cohort to determine the limited efficacy of the INSPIRE-intervention. 

Countries

Netherlands

Contacts

Public ContactB. Visser

Hogeschool van Amsterdam

p.keessen@hva.nl0616389451

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Jul 23, 2026