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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Functional exercise class | Experimental | Functional exercise class 45 mins twice weekly from week 12 to week 18 |
|
| Usual Care Group | Placebo Comparator | Usual Care |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Functional exercise class | Procedure | Functional exercise class running twice weekly for six weeks from week 12 to week 18 |
|
| Measure | Description | Time Frame |
|---|---|---|
| WOMAC Western Ontario and Mc Master osteoarthritis index questionaire | Multi dimensional self administered health status instrument used to measure changes in the dimensions of pain stiffness and function. | 3 YEARS |
| Measure | Description | Time Frame |
|---|---|---|
| Six minute walk test, | Physical performance test used to measure the distance covered in a set timeframe. | 3 years |
| Short form SF- 12 | 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. |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Brenda M Monaghan, BSc, MSc | HSE Ireland | Principal Investigator |
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| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27126617 | Derived | Monaghan B, Cunningham P, Harrington P, Hing W, Blake C, O' Dohertya D, Cusack T. Randomised controlled trial to evaluate a physiotherapy-led functional exercise programme after total hip replacement. Physiotherapy. 2017 Sep;103(3):283-288. doi: 10.1016/j.physio.2016.01.003. Epub 2016 Feb 15. | |
| 23190932 | Derived |
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| usual care group | Procedure | Usual care group adhere to post operative instructions given on discharge from hospital |
|
| 3 YEARS |
| HiP Abduction Strength Dynamometry | 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. | 3 years |
| Real time ultrasound imaging of the gluteus medius muscles | 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. | 3 years |
| Monaghan B, Grant T, Hing W, Cusack T. Functional exercise after total hip replacement (FEATHER): a randomised control trial. BMC Musculoskelet Disord. 2012 Nov 28;13:237. doi: 10.1186/1471-2474-13-237. |