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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01218282
Other study ID # ExTCOPD01
Secondary ID
Status Completed
Phase N/A
First received October 7, 2010
Last updated October 26, 2010
Start date January 2008
Est. completion date March 2010

Study information

Verified date October 2010
Source Università degli Studi di Ferrara
Contact n/a
Is FDA regulated No
Health authority Italy: Ethics Committee
Study type Interventional

Clinical Trial Summary

Exercise training is the key component of respiratory rehabilitation.The success of long-term program resides in the integration between exercise prescription and patients'compliance with home training. This can be difficult for patients, especially in terms of understanding the exercise intensity.

This study is designed to evaluate different methods of exercise training at home, to help understanding and maintaining the walking intensity in COPD patients. Outcome: exercise performance, daily physical activity and respiratory function.


Recruitment information / eligibility

Status Completed
Enrollment 80
Est. completion date March 2010
Est. primary completion date March 2009
Accepts healthy volunteers No
Gender Both
Age group 40 Years to 85 Years
Eligibility Inclusion Criteria:

- COPD patients. All patients are at stable state, free from an exacerbation from at least 3 months.

Exclusion Criteria:

- COPD patients with a recent history of cardiovascular disease and other diseases that would interfere with exercise performance.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • COPD
  • Pulmonary Disease, Chronic Obstructive

Intervention

Behavioral:
Home exercise training
20-30 min/day for at least 4 days/week
NO Exercise Training
No intervention

Locations

Country Name City State
Italy Pulmonary respiratory unit- University Hospital Ferrara

Sponsors (1)

Lead Sponsor Collaborator
Università degli Studi di Ferrara

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Exercise Capacity 1 year No
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