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Balance Training for Chronic Obstructive Pulmonary Disease (COPD)

Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Other: Balance training
Registration Number
NCT02080442
Lead Sponsor
Samantha Harrison
Brief Summary

The study will involve direct knowledge translation of a laboratory-based study of balance training for patients with COPD, first to the investigators PR program and then, after disseminating the results, this approach could be used to impact on clinical practice in any PR program.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
19
Inclusion Criteria
  • Diagnosis of COPD
  • Self-report of decline in balance or fall in the last 5 years or a recent near fall
  • Smoking history greater than 10 pack years
  • Are able to provide written informed consent.
Exclusion Criteria
  • An inability to communicate because of language skills, hearing or cognitive impairment
  • Evidence of a neurological or musculoskeletal condition that severely limits mobility and postural control (e.g., cerebrovascular accident, advanced Parkinson's disease, amputation).

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Chronic Obstructive Pulmonary DiseaseBalance training-
Primary Outcome Measures
NameTimeMethod
Berg Balance Scale (BBS)at 6 weeks

The BBS was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks.

Timed Up and Go (TUG):at 6 weeks

The TUG was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks.

Secondary Outcome Measures
NameTimeMethod
The Balance Evaluation Systems Test (BESTest)at 6 weeks

The BESTest was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks.

Activity-specific Balance Confidence (ABC) Scaleat 6 weeks

The ABC scale was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks.

Trial Locations

Locations (1)

West Park Healthcare Center

🇨🇦

Toronto, Ontario, Canada

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