- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04748718
Serial Movement Assessment in Collegiate Athletes Who Perform Injury Prevention Training
March 29, 2024 updated by: Eleanor Beltz, Northern Vermont University
Serial Movement Assessment in Athletes Who Perform Injury Prevention Training
Athletic injury can result in decreased athletic performance or removal from sport participation.
There may also be psychological and financial impacts of athletic injury.
Additionally, there can be long-term consequences, such as increased risk of subsequent injury or arthritis.
Therefore, determining ways to prevent athletic injury from occurring is critical.
Movement quality during sport is related to injury risk.
Athletes who move poorly are generally at increased risk of injury compared to athletes who move well.
Movement quality can be improved through exercise-based injury prevention training, thereby decreasing injury risk.
This purposed of this study is to evaluate movement quality multiple times over the course of an athletic season in collegiate athletes who perform injury prevention training.
The hypothesis is that movement quality will improve over the course of an athletic season.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Neuromuscular control, or quality of movement, during sport is related to injury risk.
Athletes who move poorly are generally at increased risk of injury compared to athletes who move well.
Neuromuscular control can be improved through exercise-based injury prevention training (called preventive training programs, or PTPs), thereby decreasing injury risk.
Neuromuscular control is dynamic and therefore should be evaluated regularly; however, no study has serially evaluated neuromuscular control in athletes who perform PTPs.
The overall objective of the proposed study is to longitudinally evaluate multiple aspects of neuromuscular control (i.e., movement quality, balance) across several time points during a single athletic season in collegiate athletes who perform PTPs.
Therefore, two specific aims are proposed: Specific Aim 1: Evaluate neuromuscular control at multiple time points during an athletic season in collegiate athletes who perform PTPs.
Specific Aim 2: Evaluate multiple measures of neuromuscular control over the course of an athletic season in collegiate athletes who perform PTPs.
A field-based, experimental, cohort study will be used to address both specific aims.
Subjects will be recruited from NCAA-Division III men's and women's soccer, volleyball and basketball teams.
Neuromuscular control will be assessed four times during the athletic season using the Landing Error Scoring System (LESS), the Balance Error Scoring System (BESS), and the Star Excursion Balance Test (SEBT).
The LESS evaluates movement quality, while the BESS and the SEBT evaluate static and dynamic balance, respectively.
Subjects will perform PTPs for about 10 minutes/day, at least 4 days/week.
Study Type
Interventional
Enrollment (Actual)
62
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Vermont
-
Johnson, Vermont, United States, 05665
- Northern Vermont University
-
-
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
18 years to 24 years (Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- National Collegiate Athletics Association (NCAA) Division III Athlete
- Coach and athletic trainer elect to receive injury prevention services
- Ages 18-24
Exclusion Criteria:
-Does not participate on NCAA Division III Athletic Team
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
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Injury Prevention Arm
exercise-based neuromuscular training injury prevention program
|
~10-minute, 4+ times/week exercise-based injury prevention program.
Includes flexibility, strengthening, balance, agility and plyometric exercises.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Landing Error Scoring System (LESS) Score
Time Frame: assessing change over 3 timepoints: baseline (week 0), midseason (weeks 4-6), end-of-season (weeks 10-12)
|
number of errors; scale is 0-17; lower score indicates better outcome
|
assessing change over 3 timepoints: baseline (week 0), midseason (weeks 4-6), end-of-season (weeks 10-12)
|
Balance Error Scoring System (BESS) Score
Time Frame: assessing change over 3 timepoints: baseline (week 0), midseason (weeks 4-6), end-of-season (weeks 10-12)
|
number of errors; scale is 0-60; higher score indicates worse outcome
|
assessing change over 3 timepoints: baseline (week 0), midseason (weeks 4-6), end-of-season (weeks 10-12)
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Eleanor Beltz, PhD, ATC, Northern Vermont University
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)
August 17, 2021
Primary Completion (Actual)
March 29, 2022
Study Completion (Actual)
March 29, 2022
Study Registration Dates
First Submitted
January 31, 2021
First Submitted That Met QC Criteria
February 8, 2021
First Posted (Actual)
February 10, 2021
Study Record Updates
Last Update Posted (Actual)
April 1, 2024
Last Update Submitted That Met QC Criteria
March 29, 2024
Last Verified
March 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Beltz FAW2122 NMC PTP
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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