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Clinical Trials/NCT02223962
NCT02223962
Completed
Not Applicable

The Effects of a Physical Activity Counseling Program Immediately After an Exacerbation in Patients With COPD.

KU Leuven1 site in 1 country30 target enrollmentMarch 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COPD Exacerbation
Sponsor
KU Leuven
Enrollment
30
Locations
1
Primary Endpoint
Improvement in physical activity
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Severe exacerbations are prevalent in a subgroup of patients with COPD and generally warrant a hospitalization. During the hospitalization, patients are extremely physically inactive with only a limited recovery one month after discharge. Physical inactivity is associated with negative health benefits. Therefore intervening in the period after and exacerbation seems useful to improve the levels of physical activity. Physical activity counseling and real-time feedback have already been applied in stable patients with COPD, with beneficial effects.The present study will investigate whether this specific intervention will help to improve the activity level in patients after an acute exacerbation. Further we investigated the effects of the intervention on improvements in functional exercise capacity.

Detailed Description

After signing the informed consent, the patients will be randomized into a control group, receiving usual care, or the intervention group receiving real-time feedback and physical activity counseling. Intervention: Physical activity counseling will be provided by 3 weekly telephone contacts based on the step count from the Fitbit Ultra. In agreement with the patient and based on the step counts a patients provided, a new goal for the next week was set. The goal was to strive for the highest possible level of physical activity during one month.

Registry
clinicaltrials.gov
Start Date
March 2013
End Date
May 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
KU Leuven
Responsible Party
Principal Investigator
Principal Investigator

Marc Decramer

Prof. Dr.

KU Leuven

Eligibility Criteria

Inclusion Criteria

  • Signed Informed Consent
  • Chronic Obstructive Lung Disease (Tiff\<70%)
  • Hospitalized because of exacerbation
  • Capable of working with electronic devices

Exclusion Criteria

  • Orthopedic/Neurologic problems making it difficult to be active
  • Participation in a rehabilitation program

Outcomes

Primary Outcomes

Improvement in physical activity

Time Frame: 1 month

The Dynaport MoveMonitor, a valid device in patients with COPD, was used to accurately measure the level of physical activity. The device was provided 3 times to the patients (baseline, after 2 weeks, after 1 month). The amount of steps, measured by this device, was used as the outcome measure.

Secondary Outcomes

  • Improvement in functional exercise capacity(1 month)

Study Sites (1)

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