Shoe inserts for lateral hip pain: The GluTeS Trial
- Conditions
- Greater trochanteric pain syndromeLateral hip painGluteal tendinopathyTrochanteric bursitisMusculoskeletal - Other muscular and skeletal disordersPhysical Medicine / Rehabilitation - Physiotherapy
- Registration Number
- ACTRN12620000385943
- Lead Sponsor
- a Trobe University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 60
(i) aged 18 years or older;
(ii) symptoms for at least 3 months;
(iii) primary pain located over the lateral hip;
(iv) average pain intensity over the previous week of 3 or more on an 11-point numerical rating scale; and
(v) GTPS diagnosis confirmed via clinical assessment: (a) pain reproduced on palpation of the greater trochanter; (b) pain reproduced on the Flexion, Abduction and External Rotation (FABER) test; (c) pain on one of the following: single leg stance test, resisted hip abduction, external de-rotation test.
(i) Signs of intra-articular hip pathology; (ii) previous hip surgery on the symptomatic side; (iii) low back or other lower limb injury requiring management by a medical professional, or time off sport, work or leisure over the last three months; (iv) any neurological disorders; (v) any form of systemic arthritis; (vi) currently regularly wearing contoured shoe inserts; (vii) any foot disorder precluding wearing of shoe inserts; (viii) corticosteroid injection into hip region within previous 3 months; (x) currently undergoing treatment including physiotherapy, osteopathy or chiropractic; (ix) low-English speaking proficiency such that unable to comprehend study assessment requirements.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Perceived overall change in the participant's lateral hip pain will be assessed a Global Rating of Change Scale (GRCS). This will be a 7-point Likert scale (‘much better’, ‘better’, ‘a little better’, ‘same’, ‘a little worse’, ‘worse’, ‘much worse’) [12 weeks post-intervention commencement <br>]
- Secondary Outcome Measures
Name Time Method