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One Team: Changing the Culture of Youth Sport With Pregame Safety Huddles

Not Applicable
Completed
Conditions
Concussion, Brain
Interventions
Behavioral: Pre-game Safety Huddles
Registration Number
NCT04099329
Lead Sponsor
Seattle Children's Hospital
Brief Summary

Randomized controlled trial of a behavioral intervention (Pre-Game Safety Huddles) designed to study the impact of huddles on concussion safety in youth sport, primarily regarding intention to report concussive symptoms.

Detailed Description

More than 1 million youth sustain a sport-related concussion (SRC) each year. The middle school age range is particularly concerning because it is a time when children have both a unique susceptibility to brain injury and high participation rates in organized sports with concussion risk, such as soccer and football. There are two avenues to decrease concussion risk: (1) minimizing the number and force of collisions to decrease concussion incidence (primary prevention) and (2) improving concussion identification to decrease morbidity (secondary prevention). The goal of this study is to utilize Pre-Game Safety Huddles to discuss sportsmanship (primary prevention) and concussion reporting (secondary prevention) with a goal of improving concussion safety.

To assess the efficacy of Pre-Game Safety Huddles as a tool for injury prevention, we will conduct a Randomized controlled trial with youth sport teams. We will recruit leagues in the Seattle area (girls' soccer, boys' soccer and football) and randomize them to either intervention or control. Coaches in the intervention group will then be trained to lead Pre-Game Safety Huddles before each game over the course of the season (9-12 weeks). Youth and coaches will be surveyed at three time points and data will be analyzed to determine impact of the intervention on two outcomes: 1) expectations regarding reporting concussive symptoms (CR-E) and 2) expectations regarding engaging in potentially injurious play (IP-E).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
500
Inclusion Criteria
  • Participating on a team in one of the recruited leagues and willing to complete surveys
Exclusion Criteria
  • Not willing to complete surveys

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pre-game Safety HuddlesPre-game Safety HuddlesPre-game safety huddles will occur before each game and athletes and coaches will be surveyed.
Primary Outcome Measures
NameTimeMethod
Change, Expectations regarding concussion reporting (CR-E)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey of Athlete expectations regarding reporting concussive symptoms

Secondary Outcome Measures
NameTimeMethod
Change, Perceived coach, parent and peer norms regarding concussion reporting (PN-PWCS)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey, Athlete perception of norms regarding concussion reporting

Change in Perceived coach (TN-C), parent (TN-P) and peer norms (TN-T) regarding sportsmanshipBaseline, 4-6 weeks, 9-12 weeks

Self-report survey, Athlete perception of norms regarding sportsmanship

Change, Youth sport values (YSV)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey, Athlete values regarding sport participation

Performed behavior, concussion reporting (PB--CR)9-12 weeks

Self-report survey, Athlete concussion symptoms following potential concussion during season

Self-report of concussion diagnosis9-12 weeks

Athlete report of concussion diagnosis during the season

Change, Expectations of engaging in potentially injurious play (IP-E)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey of Athlete rating of expectations of engaging in potentially risky sport behavior

Change, Expectations regarding reporting teammate concussion (bystander reporting) (E-BR)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey, Athlete intention to report teammate concussive symptoms

Change, Prosocial and Antisocial Behavior in Sport Scale (PABSS)Baseline, 4-6 weeks, 9-12 weeks

Self-report survey, Standardized measure of sportsmanship

Acceptability of Intervention Measure (AIM-2) and Feasibility of Intervention Measure (AIM-2, FIM-2)9-12 weeks

Self-report survey, Standardized measures of acceptability and feasibility

Trial Locations

Locations (1)

Sara P Chrisman

🇺🇸

Seattle, Washington, United States

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