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| Sponsor: | University of British Columbia |
|---|---|
| Collaborator: |
Michael Smith Foundation for Health Research |
| Information provided by (Responsible Party): | University of British Columbia |
| ClinicalTrials.gov Identifier: | NCT00426881 |
Purpose
Primary Objectives:
1. To ascertain whether a 12-month, twice-weekly or once-weekly resistance training (RT) program will significantly improve executive function in community-dwelling women aged 65 to 75 years old compared with a 12-month, twice-weekly stretch and relax (S & R) program (shame exercise). We will assess executive function by standard neuropsychological tests.
Secondary Objectives:
| Condition | Intervention |
|---|---|
|
Healthy |
Behavioral: Exercise Training Behavioral: Exercise training |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Single Blind (Subject) Primary Purpose: Prevention |
| Official Title: | The Effect of Resistance Training on Cognitive Performance, Cortical Plasticity, and Fall Risk in Women Aged 65-75 Years Old: A 12-Month RCT |
| Estimated Enrollment: | 155 |
| Study Start Date: | January 2007 |
| Estimated Study Completion Date: | June 2012 |
| Estimated Primary Completion Date: | June 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
Twice weekly resistance training for 52 weeks.
|
Behavioral: Exercise Training
Twice weekly resistance training for 52 weeks.
|
|
Experimental: 2
Once weekly resistance training for 52 weeks.
|
Behavioral: Exercise training
Once weekly resistance training for 52 weeks.
|
|
Experimental: 3
Twice weekly balance and tone training for 52 weeks.
|
Behavioral: Exercise training
Twice weekly resistance training for 52 weeks.
|
Primary Research Question: Does resistance training (RT) significantly improve cognitive function, specifically executive function in older women with a Mini-Mental State Examination (MMSE) score equal to or greater than 24 (i.e., cognitively intact) compared with a stretch & relax (S & R; control) program?
Secondary Research Questions:
RESEARCH PLAN:
Study Design: A 12-month, single-blinded, randomized controlled trial. Participants: 155 cognitively-intact (i.e., MMSE score > 24), right-handed, sedentary community-dwelling women, aged 65 to 75 years.
Measurement: Measurements will take place at baseline, six month, and trial completion. Standard neuropsychological testing and physiological fall risk assessment will occur at all three measurement sessions. A subset of the participants (20 from each experimental group) will undergo fMRI assessment at baseline and trial completion only. Exercise Classes: Participants will be randomized to a 12-month, twice-weekly or once-weekly RT program or stretch & relax program (control). All exercises will be offered at a Vancouver YMCA with whom we have partnered previously. Sample Size Justification: The sample size of 50 per experimental group (i.e., N = 155) is based on the primary end point of this study, cognitive performance of executive function. SUMMARY: Falls are a major challenge for the senior population. To date, no intervention has significantly reduced falls among those with cognitive impairment. Our immediate primary goal is to test whether RT can improve cognitive performance of executive function; impaired executive function are associated with injurious falls. If this proposed exercise trial proves successful, the RT intervention will be trialed in the future in a larger study powered for falls.
Eligibility| Ages Eligible for Study: | 65 Years to 75 Years |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Contacts and Locations| Canada, British Columbia | |
| Vancouver Coastal Health Research Institute Research Pavilion | |
| Vancouver, British Columbia, Canada, V5Z 1L8 | |
| YMCA | |
| Vancouver, British Columbia, Canada, V5Y 2Z5 | |
| Principal Investigator: | Teresa Liu-Ambrose, Ph.D | University of British Columbia |
More Information
| Responsible Party: | University of British Columbia |
| ClinicalTrials.gov Identifier: | NCT00426881 History of Changes |
| Other Study ID Numbers: | H06-03216, ORSIL 06-1737, ORSIL 05-6933 |
| Study First Received: | January 23, 2007 |
| Last Updated: | September 28, 2011 |
| Health Authority: | Canada: Health Canada |
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Exercise Resistance training |