Hip Surgery Corrective
Conditions
Keywords
Total hip replacement, Functional exercise class, Randomised controlled trial
Brief summary
The aim of this research project is to evaluate the efficacy of a specific functional exercise programme to improve pain, stiffness and physical function in patients post total hip replacement from week 12 to week 18 post surgery.
Detailed description
This will be a single blind randomised controlled trial with two arms. 70 subjects post primary total hip replacement will be randomised either to a functional; exercise group (n=35) or to a control group following usual care (n=35). Blinded outcome assessments will be carried out on all subjects by the principal investigator using the Western Ontario and Mc Master arthritis index on day 5 , week 12 aand week 18. Secondary outcomes measurements will also be collated at week 12 and week 18 including SF 12, 6 min walk test, Dynamometry, and a blinded radiologist will also measure glut med cross sectional area using real time ultrasound at week 12 and week 18.
Interventions
PROCEDUREFunctional exercise class
Functional exercise class running twice weekly for six weeks from week 12 to week 18
PROCEDUREusual care group
Usual care group adhere to post operative instructions given on discharge from hospital
Sponsors
Health Service Executive, Ireland
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* 12 weeks post primary THR for osteoarthritis * Age 50 years and above * Able to read and understand and instructions in English * Willing to attend classes twice weekly for 8 weeks * Able to participate in an exercise programme without physical assistance * Able to Mobilize independently 15m without crutches and /or stick -Passed by the referring Orthopaedic Consultant as suitable for inclusion at six week appointment -
Exclusion criteria
* Medically unstable * Any central or peripheral nervous system deficits * Any underlying terminal disease -Any suspicion of infection following joint replacement -
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| WOMAC Western Ontario and Mc Master osteoarthritis index questionaire | 3 YEARS | Multi dimensional self administered health status instrument used to measure changes in the dimensions of pain stiffness and function. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Six minute walk test, | 3 years | Physical performance test used to measure the distance covered in a set timeframe. |
| Short form SF- 12 | 3 YEARS | Self completed questionaire that measures health status and quality of life under eight multi item scales measuring physical function, bodily pain, role limitation due to physical health problems, general health, vitality, social function, role limitation due to emotional problems and mental health. |
| HiP Abduction Strength Dynamometry | 3 years | Assessment scale of ability to maintain balance both statically and whilst performing various functional tasks will be completed by the principal investigator at week 12 and repeated for all patients at week 18. |
| Real time ultrasound imaging of the gluteus medius muscles | 3 years | Patients will be scanned by a blinded radiologist to measure cross sectional area of the gluteus medius muscle at 12 weeks and again at 18 weeks. |
Outcome results
None listed