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RecruitingNCT07472400Updated May 5, 2026

Mobility, Strength, and Functional Outcomes Before Surgery, at 3 Months, and at 6 Months After Hip Arthroscopy for Femoroacetabular Impingement Syndrome

An observational study in Femoroacetabular Impingement Syndrome and Healthy Participants, sponsored by University of Liege. Recruiting at 1 site in Belgium. Open to participants aged 18 Years to 40 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-05.

Sponsored by University of Liege · Observational

From the registry’s dates

  • Started Mar 2026; still recruiting 8 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
60
Ages
18 Years to 40 Years
Sex
All
01

Study summary

The aim of this study is to identify the factors associated with successful rehabilitation following hip arthroscopy for femoroacetabular impingement syndrome and to highlight any persistent functional deficits at different key stages of rehabilitation. This is a controlled multi-observational study. The pathological hip of patients will be compared to their second healthy hip as well as to a healthy control group.

Assessments of mobility, strength, functional tests, and questionnaire submissions will take place before the intervention and 3 and 6 months after the intervention.

02

Conditions studied

  • Femoroacetabular Impingement Syndrome
  • Healthy Participants

Keywords

  • Femoroacetabular impingement syndrome
  • Physical impairments
  • Questionnaires
  • Strength
  • mobility
03

In context

Femoracetabular Impingement

116 studies on the registry are indexed under Femoracetabular Impingement; 37 are open to participants now.

This study's planned enrollment of 60 is below the median of 88 across 37 observational studies indexed under Femoracetabular Impingement.

Browse Femoracetabular Impingement studies →

Lead sponsor

University of Liege is the lead sponsor of 251 studies on the registry; 50 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adults aged 18-40 years will be recruited. The patient group will include individuals diagnosed with femoroacetabular impingement syndrome who are scheduled to undergo hip arthroscopy by specialized surgeons. A healthy control group without a history of hip pathology will be recruited from the local community matched as closely as possible to the patient group for demographic parameters.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Subjects with femoroacetabular impingement syndrome, with corresponding clinical symptoms and signs, as well as validation by imaging
  • Subjects who have already consulted a surgeon specializing in hip arthroscopic surgery and whose surgery is planned to treat femoroacetabular impingement syndrome
  • Subjects aged between 18 and 40

Exclusion criteria

Exclusion Criteria:

  • History of rheumatic disease, dysplasia or pediatric disease affecting the hip (Legg-Calvé; superior femoral epiphysiolysis)
  • Subject who has already undergone surgery on the hip joint
  • Subjects with a history of injury to the muscles involved in the assessments within the last year
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
60 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patient groups: 30 subjects with femoroacetabular impingement syndrome
  • Control group : 30 subjects with healthy hips
06

What researchers measure

Primary outcomes

  1. Muscle strength in Nm

    Muscular strength is measured using a fixed dynamometer

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

  2. Hip mobility in degree

    Hip mobility is measured using an electronic goniometer

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

  3. Functional results on the Y Balance Test

    The functional results of the Y balance test will be measured using the composite score.

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

  4. Functional results in the single-leg squat test

    The functional results of the single-leg squat test will be measured using the SIngle-leg squat Movement Performance scaLe for Individuals with FemoroAcetabular Impingement syndrome (SIMPLAI-FAI). The score on this scale ranges from 0 to 8. A higher score indicates a better functional outcome.

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

  5. Measurements of patient-reported outcomes using the Hip-Return to Sport After Injury Scale (HIP-RSI)

    Analysis of scores obtained on the HIP-RSI questionnaire. This questionnaire assesses psychological readiness to resume sports activities following hip surgery. It consists of six items, and the final score ranges from 0 to 100. A higher score indicates greater psychological readiness to return to sports activities.

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

  6. Measurements of patient-reported outcomes using the International Hip Outcome Tool-12 (iHot-12) questionnaire

    Analysis of scores obtained on the iHot-12 questionnaire. This questionnaire assesses the quality of life of young, active patients suffering from hip problems. It consists of 12 items and the final score ranges from 0 to 100. A score of 100 indicates full function and no symptoms, whereas a score of zero signifies maximum limitations and extreme symptoms.

    Time frame: Pre-intervention, at 3 months and 6 months post-intervention

07

Study locations

1 of 1 sites recruiting
  • Blanc Gravier sports centers
    Sart Tilman, Liège 4000, Belgium
    Recruiting
    • Raphaël Leroy, PT, PhD candidate · Contactrleroy@uliege.be · +32491128430
08

References and documents

Individual participant data

Plan to share: No — The principal investigator behind the study project will be the only person to process the data collected during this study. There are no plans to share this data.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Mar 2026 (actual). Primary completion is estimated for Jun 2027, 15 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Mar 5, 2026
First posted
Mar 16, 2026
StartActual
Mar 1, 2026
Primary completionEst.
Jun 30, 2027
CompletionEst.
Jun 30, 2027
Last update
May 5, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on May 5, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07472400
Responsible party
Raphael Leroy (Physiotherapist and PhD Candidate, University of Liege) — Principal investigator
First posted
Mar 16, 2026
Start date
Mar 1, 2026
Primary completion
Jun 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
May 5, 2026

Study contacts

Raphaël Leroy, PT, PhD candidate
Contact
rleroy@uliege.be
+32491128430

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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