E-health for optimization of the multidisciplinairy COPD care

Completed

• Conditions: Chronic Obstructive Pulmonary Disease (COPD); emphysema; 10046304

• Registration Number: NL-OMON39066
• Lead Sponsor: niversitair Medisch Centrum Utrecht

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 140

Inclusion Criteria

- Age 40 years and over
- Suffering from COPD (GOLD stage 2 and 3), 30% <= FEV1 < 80%, FEV1/FVC < 70% after bronchodilation.
- Completed rehabilitation program with a duration of at least 3 months
- Living at home independently
- signed informed consent

Exclusion Criteria

- suffering from a co-morbidity that influences daily physical activity
- use of aid for mobility
- Stopped temporarily with rehabilitation program
- experienced an exacerbation resulting in hospitalization in the last 6 months

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Performed daily physical activity measured with the multisensor armband<br /><br>(SenseWear).<br /><br>Main parameter: number of steps per day. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>• Dyspnoe (measured with the CRQ-SAS)<br /><br>• Longfunction (FEV1, FVC after bronchodilatation)<br /><br>• Physical capacity (measured with the six minute walk test)<br /><br>• Body mass index (length/weight^2)<br /><br>• Medication usage (measured by usageoverview of pharmacist)<br /><br>• Exacerbations (number during the study)<br /><br>• Use of mobile phone application (days used/ total study days (6 mos),<br /><br>measured by the website)<br /><br>• Effective guidance by health care provider (number of messages sent by<br /><br>patient and physiotherapist)</p><br>