Your session is about to expire
← Back to Search
Movement Pattern Training for Femoroacetabular Impingement
Study Summary
This trial is comparing the effects of two different treatments for hip disorders that can lead to osteoarthritis. They will be looking at patient-reported outcomes and targeted impairments to see which treatment is more effective.
- Hip Groin Pain
- Femoroacetabular Impingement
- Dysplasia
- Hip Disorder
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
Find a Location
Who is running the clinical trial?
Frequently Asked Questions
Who has access to participate in this clinical trial?
"This trial seeks 33 young adults (age 18-40) experiencing hip joint pain and related groin discomfort, who also have a modified Harris Hip Score lower than 90. Additionally, they must report their intensity of suffering as 3/10 or higher on the Pain Scale Index, demonstrate protective sensation in the feet upon examination, and display frequent symptoms over the last twelve months."
Is participation in this trial open to individuals of all ages, or are there any age restrictions?
"According to the stated selection criteria, applicants aged 18-40 are eligible for this medical trial. Additionally, 4 different studies have been made available for individuals below the age of consent and 5 trials are taking place with senior citizens over 65 years old."
Are there any open recruitment opportunities for this research project?
"The clinicaltrial.gov database suggests that this particular medical trial is no longer recruiting individuals; the study was posted on July 1st 2019 and last modified on 18th of July 2022. Nevertheless, 15 other studies are actively searching for participants right now."
What are the ultimate objectives of this research endeavor?
"This clinical trial is designed to measure participants' improvement in the Hip disability and Osteoarthritis Outcome Score (HOOS) Activities of Daily Living Subscale over a 13-week period. Secondary outcomes include changes in HOOS Sport and Recreation Subscale, Numeric Pain Rating Scale worst pain intensity, and HOOS activities of daily living subscale."
Share this study with friends
Copy Link
Messenger