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A pilot randomized clinical trial of physiotherapy intervention in early hip osteoarthritis

Is a physiotherapy intervention feasible for people with early hip osteoarthritis?

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000426684
Acronym
HIPO
Enrollment
18
Registered
2014-04-17
Start date
2014-05-05
Completion date
2014-10-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Hip osteoarthritis (OA) is associated with significant personal and societal burden, which is rising with increased life expectancy. Early hip OA is commonly seen during hip arthroscopic surgery, and can affect younger adults (age<55 years) with peak work and family commitments. Whilst hip arthroscopy is commonly undertaken for pain associated with early hip OA, no studies have examined best practice for post-operative rehabilitation. An effective intervention for early-onset hip OA will potentially have great personal and societal impact. The primary aim of this study is to establish the feasibility of a randomised clinical trial (RCT) of physiotherapy, targeted to improve hip joint range and hip-related symptoms in early-onset hip OA. This study is a blinded pilot RCT conforming to CONSORT guidelines. Twenty people with early hip OA who had hip arthroscopy surgery six to 12 months previously will be recruited and randomized to the intervention group (individualized manual therapy, exercise therapy and education) or the control group (education only). Eight interventions will occur for both groups over three months, with outcomes collected at baseline and three months. Primary outcome measure - feasibility of a full scale RCT. Secondary outcome measures - symptoms, quality-of-life and range-of-motion.

Interventions

Interventions Each participant will be treated by experienced physiotherapists who will be trained and proficient in both interventions (physiotherapy; education). Physiotherapy The physiotherapy intervention will be delivered in 8 sessions each of 30 minutes duration over 3-months (1/week for 4 weeks, 1/fortnight for 8 weeks). This consists of (i) manual hip joint and soft tissue mobilisation and stretching; (ii) hip muscle retraining; (iii) trunk muscle retraining; (iv) functional, proprioce

Interventions Each participant will be treated by experienced physiotherapists who will be trained and proficient in both interventions (physiotherapy; education). Physiotherapy The physiotherapy intervention will be delivered in 8 sessions each of 30 minutes duration over 3-months (1/week for 4 weeks, 1/fortnight for 8 weeks). This consists of (i) manual hip joint and soft tissue mobilisation and stretching; (ii) hip muscle retraining; (iii) trunk muscle retraining; (iv) functional, proprioceptive and sports- or activity- specific retraining; (v) enhancing physical activity; and (vi) education. Education will consist of topics including exercise, weight loss if appropriate, and appropriate stretching. This will be provided during thwe physiotherapy session. Based on our pilot data, the treatment will be tailored according to each patient’s clinical presentation (e.g. strength, pain severity, sporting and functional needs), presence of co-morbidities (e.g. back and other lower-limb pain or pathology) and progressed based on response to exercise load, thus maximising the training effects. The physiotherapist will supervise exercises during each visit for 15 minutes. A home exercise program will be performed independently at home 4 times per week for 60 minutes per session. An exercise manual will be produced and made accessible to each participant. Participants will complete a self report diary which will be checked at each visit and include adherence to home exercise program, use of medications and additional activity undertaken.

Sponsors

The University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

Inclusion Criteria: (i) aged 18-50 yr; (ii) arthroscopy for intra-articular hip pathology during the past 12 to 36 months; (iii) evidence of early-onset hip OA (defined as chondropathy greater than or equal to Outerbridge grade 1) at time of hip arthroscopy; (iv) hip-related pain > 30 on a 100mm Visual Analogue Scale (VAS).

Exclusion criteria

Exclusion Criteria: (i) pain that is not confirmed by physical examination of the hip; (ii) concurrent symptoms of hip bursitis or tendinitis; (iii) surgical complications including infection; (iv) planned lower limb surgery in the following 12 months (eg arthroplasty); (v) physical inability to weight-bear fully or undertake testing procedures; (vi) inability to understand written and spoken English.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 9, 2026