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Prospective Evaluation of Sport Activity and the Developemnt of Femoroacetabular Impingement in the Adolescent Hip

Prospective Evaluation of Sport Activity and the Developemnt of Femoroacetabular Impingement in the Adolescent Hip - PREVIEW

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON49483
Enrollment
20
Registered
2020-10-21
Start date
2020-12-01
Completion date
Unknown
Last updated
2024-04-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cam morphology Femoroacetabular Impingement (FAI)

Interventions

None listed

Sponsors

McMaster university hospital
Lead Sponsor

Eligibility

Age
12 Years to 17 Years

Inclusion criteria

Inclusion criteria: Age: 12-14 years at baseline Sex: 10 boys and 10 girls Activity level: 10 highly active children and 10 sendentary controls

Exclusion criteria

Exclusion criteria: Known hip pathology Previous hip surgery Contra-indication to undergo MRI

Design outcomes

Primary

MeasureTime frame
The primary study outcome is the incidence of radiographic cam morphology between the highly active (including sports) exposure subjects and the inactive/less active control subjects at 2 years, as determined by the dedicated MRI of the hip. We will define activity levels using the HAES questionnaire and GPS tracking. The HAES quantifies the duration, in hours, of 4 levels of activity ranging from very inactive (lying down, napping), somewhat inactive (sitting, reading, watching television, playing video games), somewhat active (walking, light chores), to very active (running, bicycling, activities leading to sweating or breathing hard) over a complete waking day. The HAES is designed for administration in the paediatric population and has been shown to be both a valid and reliable form of quantifying levels of physical activity. The exposure group (highly active, athletes) will include those that score *very active* on the HAES and report prior sporting activity. The control group will include those that score from *very inactive* to *somewhat active* and who report minimal to no prior sporting activity. A sensitivity analysis will evaluate cam morphology incidence (from baseline to 2 years) across all 4 possible scoring categories. Adult and child versions of the HAES questionnaire will be administered to ensure accuracy of reporting from subjects Radiographic signs of FAI are common in asymptomatic individuals and will therefore be interpreted along with a detailed history and physical examination. Symptomatic FAI in children and adolescents is typically characterized by anterior hip pain aggravated by flexion activities, decreased hip internal rotation, and a positive impingement sign. For the purposes of this study, physical examination will include range of motion measurements documented in the supine position by the blinded local investigator or a research assistant (using a goniometer), as well as response of provocative hip tes

Secondary

MeasureTime frame
Secondary outcomes include hip function and HRQL between subjects with a diagnosed hip deformity and no deformity at 2 years, as determined by the HOS and PedsQL questionnaires. The HOS is a self-administered hip score that was designed to capture hip function. The HOS has been shown to have the greatest clinimetric evidence for use in patients with FAI or labral tears. The HOS was developed for young adults and has been shown to be appropriate for use in adolescents with hip impingement. It has been validated in the Dutch language. The PedsQL is a validated and responsive measure of HRQL in children and adolescents, and can be used with healthy children and those with acute and chronic health conditions. The PedsQL was specifically designed to measure the core health dimensions outlined by the World Health Organization (physical, emotional, and social functioning), which will ensure adaptability in the global study. Adult and child versions of the HOS and PedsQL will be utilized to ensure accuracy of reporting.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)