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Long-term Effects of a 3-month Pedometer-based Program to Enhance Physical Activity in Patients With Severe COPD

University of Zurich (UZH) logo

University of Zurich (UZH)

Status

Completed

Conditions

COPD

Treatments

Behavioral: Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT03114241
Basec-Nr. 2016-00151

Details and patient eligibility

About

Long-term evaluation of a coaching program which helps patients with severe COPD to increase their daily step count, in addition to usual care.

Full description

Daily physical activity (PA) is a predictor of survival in the general population and has become a significant outcome measure in patients with COPD. Recent studies have demonstrated an independent association between PA, hospitalizations and mortality. Increased PA has significant benefits for patients with COPD. In most studies PA has only been assessed at one time point. Little is known about longitudinal changes in PA and data on determinants of changes in PA are scant. Moreover, information on best approaches to enhance PA in a population with decreasing PA is missing. To evaluate the long-term effect of a coaching program which is aimed at helping patients with severe COPD (FEV1<50%) to enhance their level of daily physical activity, in addition to usual care. Furthermore, this study aims to evaluate mechanisms that are responsible for changes of physical activity over time such as sociodemographic factors, lung function, comorbidities, vascular function, exacerbations, and medication.

Enrollment

74 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Informed consent
  • Age ≥ 40 years
  • Severe COPD (FEV1<50%) diagnosed according to GOLD-guidelines (www.goldcopd.org)

Exclusion criteria

  • Physical or intellectual impairment precluding informed consent or protocol adherence
  • Acute or recent (within the last 6 weeks) exacerbation of COPD
  • Attending a pulmonary rehabilitation program within the last 6 months
  • Pregnant patients

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

74 participants in 2 patient groups

Intervention
Active Comparator group
Description:
An increase in step count of 15% compared to baseline will be set as the minimal goal for each patient during 3 months.
Treatment:
Behavioral: Intervention
Control
No Intervention group
Description:
Usual care.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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