Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| San Antonio Military Medical Center | FED |
| Corewell Health East | OTHER |
| Boston Children's Hospital | OTHER |
| CHU de Quebec-Universite Laval |
Not provided
Not provided
Not provided
Not provided
The overarching goal of the study is to improve the surgical treatment outcomes of FAI, which is affecting an increasing number of military personnel and young active individuals in the general population. The proposed study will investigate critical patient, disease, and surgical treatment predictors of FAI surgery outcomes.
PROCEDURES:
Potential participants will be identified at their initial PI's outpatient clinic at which the PI will meet with the patient and determine if the patient should be treated surgically due to a diagnosis of FAI. Once the PI identifies the patient as a surgical candidate, the research study team in the clinic will approach the patient with study information to discuss. If the patient would like to participate, the patient will sign an informed consent document (assent document for minors) and begin completing study-specific information. If the patient would like to take the study documents home to consider participation, the research team member will provide his/her contact information to the patient.
SPECIFIC AIMS:
DATA COLLECTION:
Not provided
Not provided
Not provided
Not provided
| Measure | Description | Time Frame |
|---|---|---|
| Hip disability and Osteoarthritis Outcome Score (HOOS) | HOOS is a questionnaire constructed to assess patient-relevant outcomes in five separate sub-scales (pain, symptoms, activity of daily living, sport and recreation function and hip-related quality of life). HOOS is scored 0-100 with higher scores being the best outcome. | Pre operative (Baseline), change from baseline HOOS at 3 months, change from baseline HOOS at 6 months, change from baseline HOOS at 1 year, and change from baseline HOOS at 2 year. |
| Short Form Health Survey (SF-12) | The SF-12 is a shortened, validated, patient-reported survey of patient health with questions pulled directly from the longer form SF-36. SF-12 is scored 0-100 with higher scores being the best outcome. | Pre operative (Baseline), change from baseline SF-12 at 3 months, change from baseline SF-12 at 6 months, change from baseline SF-12 at 1 year, and change from baseline SF-12 at 2 year |
| Patient-Reported Outcomes Measurement Information System (PROMIS) - Pain Interference (PI) | PROMIS is a set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions. This specific PROMIS survey assesses a patient's pain interference. PROMIS - PI is scored from 38.7-83.8 with the lower scores being the best outcome. | Pre operative (Baseline), change from baseline PROMIS - PI at 3 months, change from baseline PROMIS - PI at 6 months, change from baseline PROMIS -PI at 1 year, and change from baseline PROMIS - PI at 2 year |
| Patient-Reported Outcomes Measurement Information System (PROMIS) - Physical Function (PF) | PROMIS is a set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions. This specific PROMIS survey assesses a patient's physical function. PROMIS - PF is scored from 14.7-75.6 with the higher scores being the best outcome. |
| Measure | Description | Time Frame |
|---|---|---|
| University of California Los Angeles Activity Score (UCLA Score) | UCLA Score represents a reliable tool for assessing the level of physical activity and the return to sport high functional demand after hip surgery. The UCLA Score is scored from 0-10 with higher scores being the best outcome. | Pre operative (Baseline), change from baseline UCLA Score at 3 months, change from baseline UCLA Score at 6 months, change from baseline UCLA Score at 1 year, and change from baseline UCLA Score at 2 year |
Not provided
Inclusion Criteria:
Age 14 - 40 years
Skeletally Mature
Failure of 6 weeks of conservative treatment
Primary surgery (Hip Arthroscopic Treatment)
a. Surgical treatment of FAI with hip arthroscopy
Tonnis 0 -1 OA, with greater than 2 mm of joint space
Clinical diagnosis of FAI (cam or combined; alpha >50 degrees)
Exclusion Criteria:
Not provided
Not provided
Skeletally mature patients being treated surgically for FAI after failing conservative treatment.
Not provided
| Name | Affiliation | Role |
|---|---|---|
| John C Clohisy, MD | Washington University School of Medicine | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Colorado | Aurora | Colorado | 80045 | United States | ||
| University of Iowa |
Not provided
| Type | Includes Protocol | Includes SAP | Includes ICF | Document Label | Document Date | Document Uploaded Date | Document File Name |
|---|---|---|---|---|---|---|---|
| ICF | No | No | Yes | Informed Consent Form | Jun 9, 2020 | Sep 29, 2025 |
Not provided
| OTHER |
| Mayo Clinic | OTHER |
| Twin Cities Orthopedics | OTHER |
| Regents of the University of Michigan | UNKNOWN |
| Ottawa Hospital Research Institute | OTHER |
| University of Texas Southwestern Medical Center | OTHER |
| University of Iowa | OTHER |
| University of Colorado, Denver | OTHER |
| Children's Hospital of Eastern Ontario | OTHER |
| University of Wisconsin, Madison | OTHER |
Not provided
Not provided
Not provided
| Pre operative (Baseline), change from baseline PROMIS - PF at 3 months, change from baseline PROMIS - PF at 6 months, change from baseline PROMIS -PF at 1 year, and change from baseline PROMIS - PF at 2 year |
| Patient-Reported Outcomes Measurement Information System (PROMIS) - Mobility (M) | PROMIS is a set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions. This specific PROMIS survey assesses a patient's mobility. PROMIS - M is scored from 18.2-60.2 with the higher scores being the best outcome. | Pre operative (Baseline), change from baseline PROMIS - M at 3 months, change from baseline PROMIS - M at 6 months, change from baseline PROMIS -M at 1 year, and change from baseline PROMIS - M at 2 year |
| Patient-Reported Outcomes Measurement Information System (PROMIS) - Depression (D) | PROMIS is a set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions. This specific PROMIS survey assesses a patient's depression. PROMIS - D is scored from 34.2-84.4 with the lower scores being the best outcome. | Pre operative (Baseline), change from baseline PROMIS - D at 3 months, change from baseline PROMIS - D at 6 months, change from baseline PROMIS - D at 1 year, and change from baseline PROMIS - D at 2 year |
| Patient-Reported Outcomes Measurement Information System (PROMIS) - Anxiety (A) | PROMIS is a set of person-centered measures that evaluates and monitors physical, mental, and social health in adults and children. It can be used with the general population and with individuals living with chronic conditions. This specific PROMIS survey assesses a patient's anxiety. PROMIS - A is scored from 32.9-84.9 with the lower scores being the best outcome. | Pre operative (Baseline), change from baseline PROMIS - A at 3 months, change from baseline PROMIS - A at 6 months, change from baseline PROMIS - A at 1 year, and change from baseline PROMIS - A at 2 year |
| International Hip Outcome Tool (iHot-12) | iHOT-12 is a validated 12-item short form of iHot-33. It was designed to measure the impact of hip disease in young, active patients and to measure the effect of treatment of this disease. | Pre operative (Baseline), change from baseline iHOT-12 at 3 months, change from baseline iHOT-12 at 6 months, change from baseline iHOT-12 at 1 year, and change from baseline iHOT-12 at 2 year |
| Modified Harris Hip Score (mHHS) | The mHHS is a reliable and valid tool for assessment of functional outcome, post total hip replacement in Indian patients, with a positive correlation with the standard Harris Hip Score. mHHS is scored 0-100 with higher scores being the best outcome. | Pre operative (Baseline), change from baseline mHHS at 3 months, change from baseline mHHS at 6 months, change from baseline mHHS at 1 year, and change from baseline mHHS at 2 year |
| Brief Resilience Scale (BRS) | The BRS was created to assess the ability to bounce back or recover from stress. | Pre operative (Baseline) |
| Mobility, Stability, and Pain (MSP Question) | Outcome measure to assess a patient's greatest issue with their hip. Asks a patient to rank mobility, stability, and pain from biggest problem to least problem. | Pre operative (Baseline), 3 months, 6 month |
| Iowa City |
| Iowa |
| 52242 |
| United States |
| Boston Children's Hospital | Boston | Massachusetts | 02115 | United States |
| University of Michigan | Ann Arbor | Michigan | 48106 | United States |
| Twin Cities Orthopedics | Edina | Minnesota | 55435 | United States |
| Mayo Clinic | Rochester | Minnesota | 55902 | United States |
| Washington University School of Medicine | St Louis | Missouri | 63110 | United States |
| Scottish Rite Hospital for Children | Dallas | Texas | 75219 | United States |
| San Antonio Military Medical Center | San Antonio | Texas | 78219 | United States |
| University of Wisconsin, Madison | Madison | Wisconsin | 53706 | United States |
| Children's Hospital of Eastern Ontario | Ottawa | Ontario | (+4) K1H 8L1 | Canada |
| The Ottawa Hospital | Ottawa | Ontario | Canada |
| CHU de Quebec - Universite Laval | Québec | Quebec | Canada |
| ICF_000.pdf |
| ID | Term |
|---|---|
| D057925 | Femoracetabular Impingement |
| D010003 | Osteoarthritis |
| ID | Term |
|---|---|
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D001168 | Arthritis |
| D012216 | Rheumatic Diseases |
Not provided
Not provided