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Neck Strengthening Program for the Prevention or Mitigation of Sports Concussion

Effectiveness of a Neck Strengthening Program for the Prevention or Mitigation of Sports Concussion Injuries in Student Athletes

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03237468
Acronym
PCONS
Enrollment
1500
Registered
2017-08-02
Start date
2017-08-11
Completion date
2022-07-31
Last updated
2021-02-03

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

Conditions

Concussion, Brain

Keywords

concussion, football, student, athlete, sports

Brief summary

Study looks to determine effectiveness of neck strengthening to reduce the incident, duration, and severity of sports related concussion in student athletes.

Detailed description

After recruitment, subjects will have neck strength measured as baseline in addition to doing SCAT5 for baseline and eye tracking, funding pending, in order to compare later assessment for concussion. Throughout study, subject will perform basic, unweighted and weighted neck strengthening exercises twice a week. Periodic re evaluations of neck strength will be performed in order to determine progress. Any time a subject incurs a sports related concussion, a SCAT5 assessment, and eye tracking funding pending, will be done and compared to baseline to measure severity of injury. Weekly follow ups will be done to assess duration of concussion. All measurements, assessments, and exercises are non-invasive and provide minimal risk to subjects.

Interventions

OTHERNeck strengthening exercise to prevent concussion

Neck strengthening exercise to prevent concussion in student athletes.

Sponsors

CentraCare
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
12 Years to 22 Years
Healthy volunteers
Yes

Inclusion criteria

* Involved in programmatic athletic activities with an ongoing duration of at least 4 weeks. * Written informed consent obtained by the subject or subject's legal guardian. * Written assent from subjects ages 8 years old and above * Subject is between the ages of 5 and 22 years, male or female. * Subjects from all racial and ethnic origins will have an opportunity to participate.

Exclusion criteria

\- Corrected vision less than 20/500.

Design outcomes

Primary

MeasureTime frameDescription
Effect of increase in neck strength in reducing risk of concussionOne yearNeck strength, as measured by a dynamometer, will be assessed and compared to baseline. Magnitude in strength will be analyzed in relation to incidence, severity, and duration of concussion.

Secondary

MeasureTime frameDescription
Effect of baseline neck strength on risk of concussionOne yearRisk of concussion will be analyzed in relation to baseline strength measurements to assess overall effect of neck strength.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026