ISRCTN59255714
Completed
Not Applicable
The effects of a 7-day inpatient multidisciplinary intervention, versus outpatient physiotherapy, with 3-months follow-up on the physical and functional outcomes of UK military personnel with pre-arthritic hip pain: a parallel-group randomised controlled trial
Arthritis Research UK Centre for Sport, Exercise and Osteoarthritis (UK)0 sites100 target enrollmentNovember 10, 2015
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Pre-arthritic, intra-articular hip pain and femoroacetabular impingement (FAI)
- Sponsor
- Arthritis Research UK Centre for Sport, Exercise and Osteoarthritis (UK)
- Enrollment
- 100
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
2016 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/27821103
Investigators
Eligibility Criteria
Inclusion Criteria
- •100 male military participants aged 18 to 50 will be recruited from patients attending the centre for lower\-limb rehabilitation outpatient injury assessment clinic (DMRC Headley Court), with symptoms of intra\-articular hip pain.
- •The specific inclusion criteria are:
- •1\. Anterior or lateral hip pain for at least 3 months
- •2\. Clinical signs and symptoms of pre\-arthritic intra\-articular hip pathology/FAI diagnosed by a specialist Rehabilitation/Rheumatology/Sports and Exercise Medicine Consultant Physician
- •3\. Physical examination findings or reproduction of pain in the groin or lateral hip with the log roll, anterior hip impingement test, or resisted straight leg\-raise test (see figures 2, 3 and 4 below)
- •4\. Sufficient time to keep therapeutic appointments
- •5\. Aged \= 18 years
Exclusion Criteria
- •1\. Ipsilateral hip surgery
- •2\. Inflammatory arthropathy
- •3\. Hip infection or tumour
- •4\. Hip fracture
- •5\. Existing extra\-articular hip disorders and/or any other pre\-existing hip pathology
- •6\. Major structural deformity of the hip
- •7\. Advanced degenerative disease of the hip (Tönnis classification 2\-3\)
- •8\. Any physical impairment or co\-morbidities (including cardiovascular disease) precluding the safe participation in the rehabilitation programme and/or assessment procedures
- •9\. History of congenital/adolescent hip disease
- •10\. Corticosteroid or analgesic injection intervention for hip within the previous 30 days
Outcomes
Primary Outcomes
Not specified
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