Study Results
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View full resultsBasic Information
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COMPLETED
NA
141 participants
INTERVENTIONAL
2013-01-31
2016-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Exercise and behaviour change strategies
The exercise program will include strength training, balance training and cardiovascular exercise that is individually tailored to the participants' abilities. The physical therapist will also implement strategies to assist with behaviour change, such as documenting progress in a log, participating in action planning and coping planning, and using techniques in the spirit of motivational interviewing.
Exercise and behaviour change strategies
1. cardiovascular exercise (e.g., marching, walking) for ≥10 minutes per day
2. postural retraining and balance exercises ≥3 days a week (will be encouraged to do these daily)
3. perform muscle strengthening and balance training exercises ≥ 3 days a week
4. the exercise intervention was developed using the Bone Fit program as a framework (http://www.bonefit.ca/). The physical therapist will tailor exercises and work with participant to integrate them into their day.
General health or social discussion
Participants in the control group will receive equal attention, but will not be prescribed exercise, or participate in counselling about exercise. The physical therapist will discuss topics related to general health.
No interventions assigned to this group
Interventions
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Exercise and behaviour change strategies
1. cardiovascular exercise (e.g., marching, walking) for ≥10 minutes per day
2. postural retraining and balance exercises ≥3 days a week (will be encouraged to do these daily)
3. perform muscle strengthening and balance training exercises ≥ 3 days a week
4. the exercise intervention was developed using the Bone Fit program as a framework (http://www.bonefit.ca/). The physical therapist will tailor exercises and work with participant to integrate them into their day.
Eligibility Criteria
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Inclusion Criteria
* documented height loss of ≥2cm
* historical height loss of ≥6cm
* visible hyperkyphosis
* age greater than or equal to 65 years of age
* able to understand instructions in english
* able to give informed consent (no cognitive impairment)
Exclusion Criteria
* On dialysis, known liver, kidney or malabsorption disease
* Progressive neurological disorder, unable to stand or walk for 10 metres, with/without gait aid or progressive disorder likely to prevent study completion, palliative care.
* Current participation in muscle strengthening or similar exercise program ≥ 3 times per week
* Uncontrolled hypertension or other contraindications to exercise
65 Years
FEMALE
No
Sponsors
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Canadian Institutes of Health Research (CIHR)
OTHER_GOV
University of Western Ontario, Canada
OTHER
University Health Network, Toronto
OTHER
McMaster University
OTHER
University of Melbourne
OTHER
University of British Columbia
OTHER
University of Waterloo
OTHER
Responsible Party
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Principal Investigators
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Lora Giangregorio, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Waterloo
Locations
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University of Waterloo
Waterloo, Ontario, Canada
Countries
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References
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Gibbs JC, McArthur C, Wark JD, Thabane L, Scherer SC, Prasad S, Papaioannou A, Mittmann N, Laprade J, Kim S, Khan A, Kendler DL, Hill KD, Cheung AM, Bleakney R, Ashe MC, Adachi JD, Giangregorio LM. The Effects of Home Exercise in Older Women With Vertebral Fractures: A Pilot Randomized Controlled Trial. Phys Ther. 2020 Apr 17;100(4):662-676. doi: 10.1093/ptj/pzz188.
Giangregorio LM, Thabane L, Adachi JD, Ashe MC, Bleakney RR, Braun EA, Cheung AM, Fraser LA, Gibbs JC, Hill KD, Hodsman AB, Kendler DL, Mittmann N, Prasad S, Scherer SC, Wark JD, Papaioannou A. Build better bones with exercise: protocol for a feasibility study of a multicenter randomized controlled trial of 12 months of home exercise in women with a vertebral fracture. Phys Ther. 2014 Sep;94(9):1337-52. doi: 10.2522/ptj.20130625. Epub 2014 May 1.
Related Links
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Principal Investigator
Other Identifiers
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18539
Identifier Type: -
Identifier Source: org_study_id
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