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A pilot double-blind randomised controlled trial comparing two physiotherapy interventions to treat femoroacetabular impingement.

A pilot double-blind placebo randomised controlled trial for people with femoroacetabular impingement, comparing a strengthening, education, manual therapy and fitness program with a stretching, education, manual therapy, fitness program to determine the feasibility of RCT methodology for a larger trial and determining which physiotherapy program reduces participant's pain and improves function.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615001218583
Acronym
Femoroacetabular Impingement Rehabilitation STudy-FIRST
Enrollment
24
Registered
2015-11-09
Start date
2015-12-01
Completion date
2016-08-14
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

Femoroacetabular (hip) impingement (FAI) is a painful condition that commonly affects healthy active younger adults. It can limit their ability to continue playing sport and perform normal daily activities. It can be related to extra bone formation at the hip joint known as a cam deformity. Physiotherapy is one treatment people may use to reduce their symptoms and improve their function. This study aims to investigate the feasibility of a randomised controlled trial (RCT) to reduce pain and improve function in people with FAI. The study will compare the effects of two different physiotherapy treatment interventions.

Interventions

Physiotherapy The physiotherapy intervention will be delivered in 8x 30 minute sessions delivered over a twelve week period (1/week for 4 weeks, 1/fortnight for 8 weeks). They will also attend one 60 minute supervised gym session per week. Gym sessions will be semi-standardised and reflect same program tailored to suit the individual within the physiotherapy session. Physiotherapy treatment sessions will consists of: i) manual hip mobilisation and stretching based on the persons clinical presen

Physiotherapy The physiotherapy intervention will be delivered in 8x 30 minute sessions delivered over a twelve week period (1/week for 4 weeks, 1/fortnight for 8 weeks). They will also attend one 60 minute supervised gym session per week. Gym sessions will be semi-standardised and reflect same program tailored to suit the individual within the physiotherapy session. Physiotherapy treatment sessions will consists of: i) manual hip mobilisation and stretching based on the persons clinical presentation addressing any assessed range of movement deficits in hip, knee and spinal joints; ii) hip muscle retraining tailored according to any assessed strength deficits with progression based on achievement of repetition and resistance goals in a semi-standardised strength program iii) trunk muscle retraining in same semi-standardised program iv) functional, proprioceptive and sports- or activity-specific retraining tailored to assessed sport or occupational loads within same semi-standardised program v) enhancing physical activity via a semi-standardised, 12 phase cardiovascular fitness program with progression based on achievement of training goal within set parameters for perceived effort and pain vi) education will be individualised and could include topics including exercise, weight loss if appropriate and appropriate stretching. This will be provided during the physiotherapy session. 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 information and exercise manual will be provided to each participant as well as access to a mobile phone app which contains the home exercise program. Participants will be asked to record both the number of exercises completed and any associated symptoms for each exercise. They may record this in the app or in a paper, self-report diary if they prefer. Compliance with the home program will be reviewed at each visit, as well as use of medications and additional activity undertaken.

Sponsors

La Trobe University, La Trobe Sport and Exercise Medicine Research Centre
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

Hip/groin pain of more than 6 weeks duration, Hip/groin pain on impingement test rated greater than 3/10 on Visual Analogue Scale (VAS), Alpha angle greater than60degrees evident on hip x-ray.

Exclusion criteria

Physiotherapy for their hip in the past 3 months, Previous surgery on symptomatic hip, Other systemic musculoskeletal conditions e.g. rheumatoid arthritis, Unable to perform testing procedures, Unable to commit to 12 weeks treatment program Contraindication to x-ray (if required) e.g. pregnancy

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026