Non-interventional cross-over study to reduce items of the draft PROactive tools as a measure of physical activity in daily life in patients with COPD

Non-interventional cross-over study to reduce items of the draft PROactive tools as a measure of physical activity in daily life in patients with COPD - PROactive

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON37932

Enrollment

Registered

2011-10-04

Start date

2011-10-04

Completion date

Unknown

Last updated

2024-05-06

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

None listed

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Provision of signed, written, and informed consent prior to conducting any study specific procedures 2. Men or women, >=40 years of age 3. Diagnosis of COPD (GOLD criteria: post bronchodilator FEV1/FVC

Exclusion criteria

Exclusion criteria: 1. Orthopaedic, neurological or other complaints that significantly impair normal biomechanical movement patterns, as judged by the investigator 2. Respiratory diseases other than COPD (e.g. asthma) 3. COPD exacerbation within 4 weeks prior to Visit 1 (only applicable for patients in the stable group) 4. Cognitive impairment, as judged by the investigator 5. Involvement in the planning and/or conduct of the study 6. Previous randomisation in the present study

Design outcomes

Primary

Measure	Time frame
The primary outcome parameter is the inital validation and itemreduction of the draft questionnaire.	—

Countries

Netherlands

Outcome results