Actively Recruiting

Phase Not Applicable
Age: 18Years - 50Years
All Genders
ID04795843

MovetheHip Trial: Effectiveness of Exercise and Patient Education Compared With Usual Care on Self-reported Pain in Hip Dysplasia

Led by University of Aarhus · Updated on 2026-05-15

200

Participants Needed

2

Research Sites

21 weeks

Total Duration

On this page

Sponsors

U

University of Aarhus

Lead Sponsor

R

Research Unit for General Practice, Aarhus University

Collaborating Sponsor

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

Who Can Participate

Age: 18Years - 50Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

AI-Screening

AI-Powered Screening

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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

Trial Site Locations

Total: 2 locations

1

Aarhus University Hospital

Aarhus N, Denmark, 8200

Actively Recruiting

2

Silkeborg Regional Hospital.

Silkeborg, Denmark, 8600

Actively Recruiting

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Research Team

J

Julie S Jacobsen, PhD

I

Inger Mechlenburg, DMSc

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

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).

Julie S Jacobsen, Rhiannon Evans, Kelly Morgan...

https://pubmed.ncbi.nlm.nih.gov/38915128

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...

https://pubmed.ncbi.nlm.nih.gov/36127096

Feasibility and acceptability of a six-month exercise and patient education intervention for patients with hip dysplasia: A mixed methods study.

Julie S Jacobsen, Kristian Thorborg, Dorthe Sørensen...

https://pubmed.ncbi.nlm.nih.gov/35820302