- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00896259
Effects of a Late Phase Exercise Program Following Total Hip Arthroplasty
Effects of a Late Phase Education and Exercise Program Following Total Hip Arthroplasty: A Pilot Project
A group of orthopedic physiotherapists have developed a late phase program to educate and instruct total hip replacement patients in progressive exercises appropriate for their level of recovery. The components of this program include an educational presentation, individual assessment and exercise prescription. The investigators' intent is to pilot the program using a sample of patients. The objective of this pilot project:
To examine the effects of the late phase education session and home-based exercise program in restoring hip muscle strength, gait and function
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Nova Scotia
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Halifax, Nova Scotia, Canada, B3H 2E1
- Orthopedic Clinic, QEII Health Sciences Centre, CDHA
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- unilateral primary total hip arthroplasty (THA)
- 8-12 weeks post THA
- over the age of 18
- able to walk 15m without a walking aid
- able to participate in an exercise program without physical assistance
- available for follow up as per the study protocol
- able to read and understand English and follow verbal and visual instructions
Exclusion Criteria:
- medically unstable
- have central or peripheral nervous system deficits
- have an underlying terminal disease (cancer)
- have suspicion of infection following joint replacement
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
THA control
those with THA not participating in exercise and education program
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THA exercise
those with THA and participating in exercise and education program
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Individual assessment with physiotherapist with educational information, exercise instruction and prescription provided.
Instructed to perform home exercises and walking for 12 weeks.
Will be individually tailored to participants, bi-monthly phone calls will be used to monitor and facilitate exercise and walking progression .
|
healthy control
Healthy control, people with no lower limb gait abnormalities
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
hip muscle strength
Time Frame: 8-12 weeks post THA, 6-7 months post THA
|
8-12 weeks post THA, 6-7 months post THA
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Gait
Time Frame: 8-12 weeks post THA, 6-7 months post THA
|
8-12 weeks post THA, 6-7 months post THA
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Ann Read, BScPT, MSc, CDHA
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CDHA-RS/2007-057
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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