Is Periacetabular Osteotomy Superior to Progressive Resistance Training?
NCT03941171 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 69
Last updated 2025-12-18
Summary
The primary aim of this study is to examine if Periacetabular Osteotomy (PAO) followed by 4 months of usual care followed by 8 months of progressive resistance training (PRT) is superior to 12 months of a PRT intervention in patients with hip dysplasia eligible for PAO in terms of self-reported pain on the HAGOS questionnaire. Secondary aims are to investigate changes in patient-reported symptoms, physical function in daily living, physical function in sport and recreation, hip and/or groin-related quality of life, generic health status, functional performance, muscle strength, physical activity and adverse events between PAO followed by usual care+PRT compared to PRT only. We hypothesise that in patients with hip dysplasia, PAO followed by usual care+PRT, results in significantly less pain at 12 months follow-up, compared to PRT only.
Conditions
- Hip Dysplasia
Interventions
- PROCEDURE
-
PAO
PAO will be performed as the trans-sartorial approach or the anterior pelvic approach.
- OTHER
-
Usual care after PAO
Patients commence post-operative rehabilitation as usual and follow the rehabilitation program guided by a physiotherapist specialized in hip problems until 4 months after the operation.
- OTHER
-
PRT
4 months of partly supervised progressive resistance training 2 times per week. After these 4 months (16 weeks), patients receive a free membership to a fitness center near their home address and are encouraged to train on their own 2 times per week until 12 months follow-up with one supervised session per month. The PRT program involves 10-min of warm up followed by 50-min of bilateral resistance exercises including sets of squats, hip extension, hip flexion, and hip abduction.
Sponsors & Collaborators
-
Aarhus University Hospital
collaborator OTHER -
VIA University College
collaborator OTHER -
University of Aarhus
lead OTHER
Principal Investigators
-
Lisa U Tønning, MSc · Department of Orthopedic Surgery, Aarhus University Hospital, Denmark
-
Inger Mechlenburg, DMSc, PhD · Department of Clinical Medicine, Aarhus University, Denmark
-
Ulrik Dalgas, MSc, PhD · Department of Public Health - Sport, Aarhus University, Denmark
-
Stig S Jakobsen, PhD · Department of Orthopedic Surgery, Aarhus University Hospital, Denmark
-
Kjeld Søballe, DMSc · Department of Orthopedic Surgery, Aarhus University Hospital, Denmark
-
Julie S Jacobsen, MSc · Department of Physiotherapy & Research Centre in Health and Welfare Technology, VIA University College, Denmark
-
Jan E Madsen, MD, PhD · Department of Orthopedic Surgery, Oslo University Hospital, Norway
-
Lars Nordsletten, PhD · Division of Orthopaedic Surgery, Oslo University Hospital, Oslo; Faculty of Medicine, University of Oslo, Norway
-
Tone Bere, PT, PhD · Department of Orthopedics, Oslo University Hospital Ullevaal, Norway
-
May A Risberg, PhD · Department of Orthopedics, Oslo University Hospital Ullevaal, Norway
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-07-01
- Primary Completion
- 2025-09-15
- Completion
- 2025-09-15
Countries
- Denmark
- Norway
Study Locations
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