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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00836108
Other study ID # RG20080707ArmStrategy
Secondary ID
Status Completed
Phase N/A
First received February 3, 2009
Last updated July 10, 2012
Start date February 2009
Est. completion date May 2012

Study information

Verified date July 2012
Source West Park Healthcare Centre
Contact n/a
Is FDA regulated No
Health authority Canada: Ethics Review Committee
Study type Interventional

Clinical Trial Summary

Controlling the way people with lung problems breathe during arm exercises may reduce their breathlessness during activities of daily living that require them to lift their arms (i.e. brushing their hair, putting groceries away on high shelves). The main aim of this study is to determine the effects of specific breathing strategies during arm exercise on dyspnoea in patients with chronic lung disease. Coordinating inspiration with the action of arm elevation will reduce dyspnoea during a rhythmic overhead arm activity


Recruitment information / eligibility

Status Completed
Enrollment 36
Est. completion date May 2012
Est. primary completion date May 2012
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- diagnosis of COPD including forced expiratory volume in one second < 80% predicted normal

- presence of lung hyperinflation at rest

Exclusion Criteria:

- musculoskeletal or neurological condition which could adversely affect arm activity

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
breathing strategy
Subjects will practice a rhythmic overhead arm exercise, during which they will be taught to inspire when they elevate their arms or they will be taught to expire when they elevate their arms or, a third group, will practice a rhythmic overhead arm exercise, during which they will not be provided with any instruction regarding a specific breathing pattern. The arm exercise practiced by all groups will be identical.

Locations

Country Name City State
Canada West Park Healthcare Centre Toronto Ontario

Sponsors (1)

Lead Sponsor Collaborator
West Park Healthcare Centre

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Dyspnoea during arm exercise 1 week No
Secondary Arm exercise endurance 1 week No
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