Physical Capacity Among Patients Treated With Periacetabular Osteotomy for Hip Dysplasia: a Cross-sectional Study

Musculoskeletal Diseases Clinical Trial

Official title:

Physical Capacity Among Patients Treated With Periacetabular Osteotomy for Hip Dysplasia: a Cross-sectional Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04591067
• Other study ID #: 20006975
• Status: Completed
• Start date: June 1, 2020
• Est. completion date: November 1, 2022

Study information

• Verified date: November 2022
• Source: Copenhagen University Hospital, Hvidovre
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This cross-sectional study investigates the physical capacity of patients, who have undergone a periacetabular osteotomy for hip dysplasia within the last 1-5 years.

Description:

Hip dysplasia is a common disease both worldwide and among the Danish population. The disease is characterized by a shallow and oblique acetabulum, resulting in insufficient coverage of the femoral head. The abnormalities of the dysplastic hip joint lead to altered biomechanical adaptations, highly affecting the physical capacity of patients. Studies have shown that patients with hip dysplasia experience reduced muscle strength and gait abnormalities, when compared to healthy controls.

Each year, approximately 200 Danes with hip dysplasia are treated with periacetabular osteotomy (PAO). As the preferable joint-preserving surgical treatment for younger patients with symptomatic hip dysplasia, the PAO reduces prevalence of muscle-tendon-related pain and improves hip and groin related patient-reported outcome measures (PROMs). By extension, studies report a hip survival rate of approximately 75% 12 years following PAO.

However, little is known about objective measures of physical capacity following PAO. Despite reducing muscle-tendon-related pain and improving PROMs, gait adaptations still remain and studies report no improvements in muscle strength, nor in the physical activity profile, 1 year following treatment with PAO. Thus, the field calls for research aiming to identify parameters of impaired physical capacity in patients treated with PAO. Thorough knowledge of physical capacity in these patients may contribute to the establishment of a science-based rehabilitation strategy, potentially improving physical activity, function, work capacity and quality of life.

The primary aim of this study is to analyse and identify parameters of impaired physical capacity in patients with hip dysplasia 1-5 years following treatment with PAO. Gait function, defined as peak hip extension angle and peak hip flexor moment, is chosen as the primary outcome, due to previously shown correlations between the extent of gait impairments and the Copenhagen Hip and Groin Outcome Score (HAGOS).

As recommended by the International Hip-related Pain Research Network (IHiPRN), measurements of physical capacity in patients with hip-related pain should include: clinical measures, laboratory-based measures, measures of physical activity and return to physical activity. Secondary outcomes of this study are: muscle activity during level walking and walking with inclination, endurance and pain during walking, range of motion (ROM), muscle strength, hip and muscle-tendon-related pain, radiographic measures and PROMs (present level of physical activity and sports & activity level prior to and after treatment with PAO).

We hypothesise that patients with the lowest scores of HAGOS subscales pain and sport/recreation will have the lowest physical capacity, measured as: gait impairments, reduced muscle strength and prevalence of muscle-tendon-related pain.

This is a cross-sectional study.

Thirty subjects from across the country, aged 18-40 years, who have undergone a PAO for hip dysplasia within the last 1-5 years, will be included in the study.

All testing will be performed at Copenhagen University Hospital, Hvidovre.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: November 1, 2022
• Est. primary completion date: October 1, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• Age 18 to 40 years

• BMI < 30

• Primary diagnosis of ipsilateral or bilateral hip dysplasia

• Treated with PAO for hip dysplasia unilaterally or bilaterally within 1-5 years

Exclusion Criteria:

• Retroverted acetabulum (positive posterior wall sign and ischial spine sign) treated with reversed PAO

• Total Hip Arthroplasty (THA)

• Pain management with analgesics or other medication affecting muscle function and perception of pain

• A need for walking aids to be able to walk freely

Related Conditions & MeSH terms

• Developmental Dysplasia of the Hip
• Hip Dislocation
• Hip Dislocation, Congenital
• Hip Dysplasia
• Hyperplasia
• Joint Diseases
• Musculoskeletal Diseases

Intervention

Other:
• Testing of physical capacity
This cross-sectional study will involve evaluation of physical capacity by assessment of: Gait function Muscle activity during walking Endurance during walking Hip muscle strength Hip range of motion Hip and muscle-tendon-related groin pain Hip and groin related patient-reported outcome measures (PROMs)

Locations

Country	Name	City	State
Denmark	Department of Orthopedic Surgery, Copenhagen University Hospital Amager-Hvidovre, Hvidovre, Denmark	Copenhagen	Hvidovre

Sponsors (1)

Lead Sponsor	Collaborator
Copenhagen University Hospital, Hvidovre

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Gait function	Peak hip extension angle and peak hip flexor moment	Baseline
Secondary	Gait function following fatigue	Peak hip extension angle and peak hip flexor moment following a 6-Minute walk test	Baseline
Secondary	Muscle activity	Muscle activity of hip specific muscles during level walking and walking with inclination	Baseline
Secondary	Maximal voluntary isometric hip muscle force	Adduction, abduction, flexion and extension	Baseline
Secondary	Hip and muscle-tendon-related groin pain	FADIR and FABER, modified standardized clinical entity approach	Baseline
Secondary	Hip specific patient reported outcome measures (PROMs)	Present level of physical activity and sports & activity level prior to and after treatment with PAO	Baseline