Exercise and education for patients with hip dysplasia
Official title: MovetheHip-trial: The Effectiveness of Exercise and Patient Education Compared With Usual Care on Self-reported Pain in Patients With Hip Dysplasia
Run by University of Aarhus · NCT04795843 · Data updated 2026-11-12
This study is testing if exercise and education can help people with hip dysplasia feel less pain and improve their hip function compared to regular care.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 50 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University of Aarhus Academic / other |
| Locations | 2 sites (Aarhus N and 1 other locations) |
| Status | Recruiting |
| Started | April 16, 2021 |
| Main results expected | July 2027 |
| Study ends | December 2027 |
| Registry record updated | May 15, 2026 |
| Trial ID | NCT04795843 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with radiographically verified hip dysplasia experiencing hip and/or groin pain for at least three months.
✕Probably not a fit
Patients with severe pain scores or those who have undergone major hip surgeries may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This trial investigates the effectiveness of exercise and patient education compared to usual care for patients with hip dysplasia. Participants will be randomly assigned to either the intervention group, which receives exercise and education, or the control group receiving usual care. The primary outcome is the change in self-reported pain measured by the Copenhagen Hip and Groin Outcome Score (HAGOS) over a six-month follow-up period. Additionally, secondary outcomes will assess various aspects of hip function and quality of life. A health-economic and process-evaluation study will also be conducted alongside the main trial.
Why it matters
Potential benefit: If successful, this approach could significantly reduce pain and improve quality of life for patients with hip dysplasia.
How similar studies have gone: Other studies have shown positive outcomes with exercise and education interventions for similar conditions, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Radiographically verified hip dysplasia by a Wiberg's centre edge (CE) angle of 10-25 degrees and an acetabular Index (AI) angle \>10 degrees * Hip and/or groin pain as primary pain for at least three months * Candidate for periacetabular osteotomy (PAO) but unwilling to undergo PAO, or on a waiting list for surgery (PAO) for 12 months or longer * Not candidate for PAO (negative impingement test, BMI \>25, hip osteoarthritis, age \>45 years or reduced hip range of motion) Exclusion Criteria: * Self-reported pain score \>80 points measured with Copenhagen Hip and Groin outcome score * Any major planned surgery (i.e. arthroplastic surgery or discectomy surgery) * BMI \>35 * Acetabular retroversion defined by crossover sign and posterior wall sign * Calvé Legg Perthes or epiphysiolysis * Previous pelvic/hip surgery in index limb * Previous pelvic/hip surgery within the last 2 years in contralateral limb * Previous surgery due to herniated disc or spondylodesis * Previous arthroplastic surgery in the hip, knee or ankle * Physical (pregnancy/trauma), neurological, medical or rheumatic conditions severely affecting the hip function * Inadequacy in written and spoken Danish, mental illness or other conditions affecting the ability to follow mandatory procedures for participation
Where it's running
-
Aarhus University Hospital
Aarhus N, Denmark Recruiting -
Silkeborg Regional Hospital.
Silkeborg, Denmark Recruiting
Study contacts
- Principal investigator: Julie S Jacobsen, PhD — VIA University College
- Study coordinator: Julie S Jacobsen, PhD
- Email: jsaj@via.dk
- Phone: 4551866165
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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PENG block added to spinal anesthesia in kids having hip surgery
This study tests whether adding a PENG block to spinal anesthesia can lower inflammation after hip surgery in children aged 3–8.
-
PENG plus lateral femoral cutaneous nerve block versus lumbar and sacral erector spinae plane blocks for pediatric hip surgery
This trial will test whether combining a PENG block with a lateral femoral cutaneous nerve block gives better pain relief and lowers opioid use than lumbar and sacral erector spinae plane blocks in children aged 2–16 having elective hip surgery.
-
Comparing pain management methods for hip surgery in children with cerebral palsy
This study is testing whether local anesthetic injections can help manage pain better than traditional epidural anesthesia for children with cerebral palsy after hip surgery.
-
Comparing observation and bracing for mild hip dysplasia in infants
This study tests if watching and monitoring infants with mild hip dysplasia is just as good as using braces to help them, to see if we can avoid unnecessary treatments.
-
Evaluating the safety and effectiveness of pediatric orthopedic implants
This study is testing how safe and effective orthopedic implants are for kids with fractures and limb deformities to see how they perform over time.
-
Comparing hip surgery techniques for hip dysplasia
This study is testing if adding a hip surgery to fix joint issues improves recovery for people with hip dysplasia compared to just the main surgery alone.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.