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Conservative Treatment in Patients With Symptomatic Femoroacetabular Impingement

The Effectiveness of Neuromuscular Training of the Lower Limb Muscles in Reducing the Hip Symptoms in Patients With Symptomatic Femoroacetabular Impingement: a Prospective Intervention Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02368483
Enrollment
34
Registered
2015-02-23
Start date
2014-10-31
Completion date
2017-03-31
Last updated
2019-06-18

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

Conditions

Symptomatic Femoroacetabular Impingement

Brief summary

This is a single-group, prospective, intervention study. A total of 30 participants with unilateral symptomatic femoroacetabular impingement will be included into the study. The intervention consists in neuromuscular training for the lower limb muscles (12 weeks, 2 times/week supervised training, 2 times/week home training). The training includes physical exercises routinely used worldwide in clinical settings. No control intervention group was included into the study because nowadays there is no standard conservative treatment for patients with symptomatic femoroacetabular impingement. Assessments will be performed at (1) baseline, (2) mid-intervention, (3) end-intervention, and (4) follow-up. Clinical, functional, neuromuscular and self-reported parameters will be collected during assessments.

Interventions

OTHERNeuromuscular training

Neuromuscular training for the hip and lower limb muscles.The training program is divided into 3 phases, and includes specific exercises for improving the hip range of motion, muscle strength of the hip and lower limb muscles, as well as the trunk stability and coordination. The intervention lasts 12 weeks. Patients will train 2 times/week with a physical therapist and 2 times/weeks alone at home.

Sponsors

Schulthess Klinik
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of unilateral symptomatic FAI according to clinical, radiographic and magnetic resonance imaging criteria * Living place: Canton of Zurich or neighbouring Cantons * Signed written informed consent to participate into the study

Exclusion criteria

* Previous hip surgery * Any surgery to the lower limbs in the prior 6 months * Congenital/developmental dysplasia * Hip osteoarthritis * Initiation of opioid analgesia and corticosteroid injection for hip pain within the prior 30 days * BMI \>35 kg/m2 * Significant cardiorespiratory diseases

Design outcomes

Primary

MeasureTime frameDescription
Hip Function as measured using the Hip Outcome Score questionnaireChange from Baseline in Hip Function at 12 weeksHip Function was assessed using the Hip Outcome Score. The Hip Outcome score is a questionnaire used to evaluate hip function during daily and sport activities. Two independent scores are obtained: one for activities of daily living and one for sport activities.

Secondary

MeasureTime frameDescription
Hip Muscle Strength as measured using dynamometryChange from Baseline in Hip Muscle Strength at 12 weeksHip abduction, adduction, internal rotation and external rotation isometric maximal voluntary contraction strength is evaluated with hand-held dynamometry. Hip flexion and extension isometric maximal voluntary contraction strength is evaluated with isokinetic dynamometry.
Movement Control Quality as measured using a visual rating scaleChange from Baseline in Movement Control Quality at 12 weeksOverall body movement pattern quality is visually assessed during the performance of 5 lower extremity functional tests (single-leg squat, lunge, hop lunge, single-leg bridge, single-leg ventral plank).

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026