MovetheHip Trial Comparing Exercise and Patient Education to Usual Care for Pain Relief in Adults with Hip Dysplasia
Led by University of Aarhus · Updated on 2026-05-15
200
Participants Needed
2
Research Sites
21 weeks
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of exercise combined with patient education compared with usual care in adults with hip dysplasia. The study aims to determine if patients who receive exercise and education experience different changes in self-reported hip and groin pain over six months. The trial also includes health-economic and process-evaluation studies to assess cost-effectiveness and how the intervention works in practice.
Participants are randomly assigned to one of two groups one group receives an exercise program with patient education, and the other follows usual care. The exercise group attends eight supervised training sessions over six months and performs a home-based exercise program focused on strength and stability, with exercises adjusted for difficulty and exertion. Patient education covers pain management, exercise adherence, and physical activity advice. The usual care group receives a consultation on managing hip symptoms and general exercise guidance.
During the study, participants report their pain levels using the Copenhagen Hip and Groin Outcome Score HAGOS at baseline, 3 months, and 6 months, with additional follow-ups up to 12 months and longer-term assessments planned. Researchers also measure symptoms, daily living function, sports and recreation function, physical activity participation, quality of life, hip disease impact, lower limb reach, single-leg hop distance, and hip muscle strength. The study includes monitoring of adherence and evaluations of intervention implementation, mechanisms of change, and contextual factors. Total participation includes assessments over a one-year period and long-term follow-up for up to 10 years.
CONDITIONS
Brief Title
Exercise and Patient Education Compared With Usual Care in Patients With Hip Dysplasia
Research Team
J
Julie S Jacobsen, PhD
I
Inger Mechlenburg, DMSc
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Research Unit for General Practice, Aarhus University
Collaborating Sponsor
Who Can Participate
Age: 18Years - 50Years
All Genders
Eligibility Criteria
You may qualify if you...
Radiographically confirmed hip dysplasia with Wiberg's centre edge angle of 10-25 degrees and acetabular index angle over 10 degrees
Hip and/or groin pain as main pain lasting at least three months
Candidate for periacetabular osteotomy (PAO) but unwilling to have PAO, or waiting for PAO surgery for 12 months or longer
Not a candidate for PAO due to negative impingement test, BMI over 25, hip osteoarthritis, age over 45 years, or limited hip motion
Age between 18 and 50 years
You will not qualify if you...
Self-reported pain score over 80 points on Copenhagen Hip and Groin Outcome Score
Planned major surgeries like arthroplasty or discectomy
Body mass index (BMI) over 35
Acetabular retroversion shown by crossover and posterior wall signs
Calvé Legg Perthes disease or epiphysiolysis
Previous pelvic or hip surgery on the affected leg
Pelvic or hip surgery within last 2 years on opposite leg
Previous surgery for herniated disc or spinal fusion
Previous arthroplasty surgery in hip, knee, or ankle
Severe physical, neurological, medical, or rheumatic conditions affecting hip function
Inadequate Danish language skills, mental illness, or other conditions limiting ability to follow study procedures
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Treatment
Duration - 6 months
Participants are assigned to either exercise and patient education or usual care for hip dysplasia over 6 months. The exercise group attends eight one-to-one supervised training sessions and performs home-based exercises three times a week, while the usual care group receives individual consultation on self-management and general advice on exercise and physical activity.
8 supervised training sessions and regular home-based exercise sessions over 6 months
Follow-up
Duration - 6 months
Participants are followed up to assess changes in pain, symptoms, physical function, quality of life, and hip function over 6 months, including assessments at 3 and 6 months after starting treatment.
Visits at baseline, 3 months, and 6 months for outcome assessments
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
Comparing exercise and patient education with usual care in the treatment of hip dysplasia: a protocol for a randomised controlled trial with 6-month follow-up (MovetheHip trial).
Julie Sandell Jacobsen, Kristian Thorborg, Rasmus Østergaard Nielsen...
An exercise and patient education intervention to reduce pain and physical limitations in adults with acetabular dysplasia: study protocol for a process evaluation integrated within a randomised controlled trial (the MovetheHip trial).