RecruitingNot ApplicableNCT06924164

Progressive Resistance Training for Adults With External Snapping Hip

Snappy Hip Trial: A Randomized Crossover Trial Comparing the Clinical and Cost-effectiveness of Progressive Resistance Training Compared to Usual Care on Pain for Adults With External Snapping Hip


Sponsor

Aarhus University Hospital

Enrollment

100 participants

Start Date

Jul 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

External snapping hip is characterised by an audible and painful snap during hip movement among physical active people around 15-40 years old. Progressive resistance training has been suggested as a new potential treatment path in treating patients with external snapping hip. The investigators conducted a feasibility study and found that patients reported less pain and improved their physical function, quality of life and muscle strength after 12 weeks of progressive resistance training. The overall aim of the project is to compare hip pain in patients with external snapping hip treated with progressive resistance training to a wait-and-see approach, in a randomised controlled trial. This study has the potential to establish a new and specific treatment option for patients with external snapping hip, to be used nationally and internationally.


Eligibility

Min Age: 18 YearsMax Age: 40 Years

Inclusion Criteria5

  • Age 18-40 years (10)
  • Experienced lateral hip joint "snapping" with pain discomfort within the last 14 days
  • Able to demonstrate the audible and/or visible lateral "snapping" during lateral hip joint movementor popping sound when the hip joint moves
  • Capable of commuting to the training facility
  • Proficient in reading and understanding Danish or English

Exclusion Criteria8

  • Previous surgery on the affected hip
  • Planned surgery on lower extremities within the trial period
  • Anterior or medial hip discomfort that substantially exceeds the lateral hip discomfort
  • Any contraindication to exercise
  • Neurological, rheumatoid, or mental conditions affecting the hip function
  • Ongoing active cancer treatment
  • Planned vacation for more than 14 days within the intervention period
  • Pregnancy

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Interventions

OTHERProgressive resistance training

The progressive resistance program consist of a five-minute aerobic warm-up on either an ergometer bike, treadmill or rowing machine followed by six resistance training exercises: landmine twist, walking lunges, leg press, hip abduction, hip adduction and hip flexion. All training sessions (three per week) will be supervised for the first two weeks. After that, there will be one weekly supervised training session and two self-directed sessions. The subjects will be scheduled for 36 training sessions over 12 weeks, of which 16 will be supervised. Each training session is designed based on the findings from the feasibility study and is expected to last approximately one hour. If a subject cannot perform all scheduled sessions in a week, additional sessions will be planned for the following week to obtain the 16 supervised sessions.

BEHAVIORALWaiting time

12 weeks of waiting time

BEHAVIORALSelf guided exercise

12 weeks of self guided exercise


Locations(13)

Aalborg Universitetshospital

Aalborg, Denmark

Aarhus University Hospital

Aarhus N, Denmark

Rigshospitalet

Copenhagen, Denmark

Bispebjerg og Frederiksberg Hospital

Copenhagen, Denmark

Regionshospitalet Gødstrup

Herning, Denmark

Nordsjællands Hospital - Hillerød

Hillerød, Denmark

Regionshospitalet Horsens

Horsens, Denmark

Hvidovre Hospital

Hvidovre, Denmark

Sjællands Universitetshospital - Køge

Køge, Denmark

Næstved, Slagelse og Ringsted Hospital

Næstved, Denmark

Odense Universitetshospital

Odense, Denmark

Regionshospitalet Randers

Randers, Denmark

Sygehus Lillebælt - Vejle

Vejle, Denmark

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NCT06924164