- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05068544
Adolescent Normative Sport Movement Analysis
January 31, 2024 updated by: MultiCare Health System Research Institute
The objective of this study is to collect baseline data from a normative population of adolescents who participate in organized "land-based" sports, that gender and age matches some of the population of patients expected to be treated at Mary Bridge Children's Therapy Services, MultiCare affiliated therapy centers, and Mary Bridge Specialty Clinics who will be seen in the Research and Movement Lab.
This project will recruit 40 patients between the ages of 13-25 years old.
Non-invasive measurements of movement patterns will be collected during common sport-related activities over a single data collection session.
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
40
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Melissa Winter, DPT
- Phone Number: 2536975268
- Email: Melissa.Winter@multicare.org
Study Locations
-
-
Washington
-
Puyallup, Washington, United States, 98372
- Recruiting
- Mary Bridge Children's Therapy Unit
-
Contact:
- Adam Cyr, Phd
- Phone Number: 253-697-5402
- Email: ajcyr@multicare.org
-
Contact:
- Brenna Brandsma, DPT
- Phone Number: 253-697-5268
- Email: brenna.brandsma@multicare.org
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years to 25 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
A group of 40 neurotypical and healthy adolescent subjects who participate in organized "land-based" sports will be recruited for this data collection.
Adolescent subjects will be ages 13-25 with an equal number of male and female (gender assigned at birth).
Description
Inclusion Criteria:
- Age between 13-25 years.
- Participate in a "land-based" organized sport in the last 1 year with intent on continued participation in the next year.
- Perform sport-related activities such as running/sprinting, cutting maneuvers, and jumping.
- Tolerate adhesive markers placed on skin and clothing.
- Willing and interested in participating.
Exclusion Criteria:
- Neuromuscular disorders such as cerebral palsy, muscular dystrophy, myotonic dystrophy, spinal muscular atrophy, peripheral neuropathy, or other generalized muscle and/or nerve issues.
- Currently undergoing treatment or receiving medication that affects movement.
- Requires ankle/knee bracing to safely perform running, sprinting, jumping activities.
- History of orthopedic surgery to lower limbs.
- In last 6 months: receiving/seeking medical treatment for injury.
- Difficulty performing sport-related activities.
- Pain that has inhibited participation in sports/daily activities in the last 3 months.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Observation-based movement analyses
Time Frame: Baseline
|
The purpose of the sports normative data collection is to develop a baseline database from a normative population of adolescents who participate in organized "land-based" sports.
Observation-based analyses are performed with a trained practitioner identifying events (e.g.
max knee flexion) and general joint position (e.g.
knee valgus) through visual observation, or with the aid of video.
This project will recruit 40 patients between the ages of 13-25 years old.
Non-invasive measurements of movement patterns will be collected during common sport-related activities over a single data collection session.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 21, 2021
Primary Completion (Estimated)
December 31, 2024
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
September 23, 2021
First Submitted That Met QC Criteria
October 4, 2021
First Posted (Actual)
October 6, 2021
Study Record Updates
Last Update Posted (Estimated)
February 2, 2024
Last Update Submitted That Met QC Criteria
January 31, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2021/06/2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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