Chronic Obstructive Pulmonary Disease Clinical Trial
Official title:
Balance Training for COPD in Pulmonary Rehabilitation (PR): An Effectiveness Study
Verified date | March 2014 |
Source | West Park Healthcare Centre |
Contact | n/a |
Is FDA regulated | No |
Health authority | Canada: Ethics Review Committee |
Study type | Observational |
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.
Status | Completed |
Enrollment | 19 |
Est. completion date | February 2014 |
Est. primary completion date | February 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A and older |
Eligibility |
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). |
Observational Model: Cohort, Time Perspective: Cross-Sectional
Country | Name | City | State |
---|---|---|---|
Canada | West Park Healthcare Center | Toronto | Ontario |
Lead Sponsor | Collaborator |
---|---|
Samantha Harrison | Ontario Lung Association |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Balance training progression: the training prescription and progression will be recorded | at 6 weeks | No | |
Other | Therapists' and the participants' satisfaction | Patients completed a questionnaire following completion of the balance training which took place thrice weekly for a period of 6 weeks. The focus group was conducted at the end of study recruitment. |
at 6 weeks | No |
Other | Safety: any adverse events associated with balance training will be recorded | at 6 weeks | Yes | |
Other | Applicability and adherence | at 6 weeks | No | |
Other | The Six-Minute Walk Test (6MWT) | The 6MWT was assessed by the physiotherapists responsible for delivering the PR program. The PR programs runs over 6 weeks. | at 6 weeks | No |
Primary | Berg Balance Scale (BBS) | The BBS was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks. | at 6 weeks | No |
Primary | Timed Up and Go (TUG): | The TUG was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks. | at 6 weeks | No |
Secondary | The Balance Evaluation Systems Test (BESTest) | The BESTest was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks. | at 6 weeks | No |
Secondary | Activity-specific Balance Confidence (ABC) Scale | The ABC scale was assessed following completion of the balance training which took place thrice weekly for a period of 6 weeks. | at 6 weeks | No |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05102305 -
A Multi-center,Prospective, OS to Evaluate the Effectiveness of 'NAC' Nebulizer Therapy in COPD (NEWEST)
|
||
Completed |
NCT01867762 -
An Effectiveness and Safety Study of Inhaled JNJ 49095397 (RV568) in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease
|
Phase 2 | |
Recruiting |
NCT05562037 -
Stepped Care vs Center-based Cardiopulmonary Rehabilitation for Older Frail Adults Living in Rural MA
|
N/A | |
Terminated |
NCT04921332 -
Bright Light Therapy for Depression Symptoms in Adults With Cystic Fibrosis (CF) and COPD
|
N/A | |
Completed |
NCT03089515 -
Small Airway Chronic Obstructive Disease Syndrome Following Exposure to WTC Dust
|
N/A | |
Completed |
NCT02787863 -
Clinical and Immunological Efficiency of Bacterial Vaccines at Adult Patients With Bronchopulmonary Pathology
|
Phase 4 | |
Recruiting |
NCT05552833 -
Pulmonary Adaptive Responses to HIIT in COPD
|
N/A | |
Recruiting |
NCT05835492 -
A Pragmatic Real-world Multicentre Observational Research Study to Explore the Clinical and Health Economic Impact of myCOPD
|
||
Recruiting |
NCT05631132 -
May Noninvasive Mechanical Ventilation (NIV) and/or Continuous Positive Airway Pressure (CPAP) Increase the Bronchoalveolar Lavage (BAL) Salvage in Patients With Pulmonary Diseases?
|
N/A | |
Completed |
NCT03244137 -
Effects of Pulmonary Rehabilitation on Cognitive Function in Patients With Severe to Very Severe Chronic Obstructive Pulmonary Disease
|
||
Not yet recruiting |
NCT03282526 -
Volume Parameters vs Flow Parameters in Assessment of Reversibility in Chronic Obstructive Pulmonary Disease
|
N/A | |
Completed |
NCT02546700 -
A Study to Evaluate Safety and Efficacy of Lebrikizumab in Participants With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 2 | |
Withdrawn |
NCT04446637 -
Acute Bronchodilator Effects of Ipratropium/Levosalbutamol 20/50 mcg Fixed Dose Combination vs Salbutamol 100 mcg Inhaler Plus Ipratropium 20 mcg Inhalation Aerosol Free Combination in Patients With Stable COPD
|
Phase 3 | |
Completed |
NCT04535986 -
A Phase 3 Clinical Trial to Evaluate the Safety and Efficacy of Ensifentrine in Patients With COPD
|
Phase 3 | |
Recruiting |
NCT05865184 -
Evaluation of Home-based Sensor System to Detect Health Decompensation in Elderly Patients With History of CHF or COPD
|
||
Completed |
NCT03295474 -
Telemonitoring in Pulmonary Rehabilitation: Feasibility and Acceptability of a Remote Pulse Oxymetry System.
|
||
Completed |
NCT03256695 -
Evaluate the Relationship Between Use of Albuterol Multidose Dry Powder Inhaler With an eModule (eMDPI) and Exacerbations in Participants With Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 3 | |
Withdrawn |
NCT04042168 -
Implications of Appropriate Use of Inhalers in Chronic Obstructive Pulmonary Disease (COPD)
|
Phase 4 | |
Completed |
NCT03414541 -
Safety And Efficacy Study Of Orally Administered DS102 In Patients With Chronic Obstructive Pulmonary Disease
|
Phase 2 | |
Completed |
NCT02552160 -
DETECT-Register DocumEnTation and Evaluation of a COPD Combination Therapy
|