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TerminatedNCT07414303POCKITUpdated Feb 17, 2026

Implementation of an Evidence-Based Educational Resource for Children With Mild Traumatic Brain Injury

An observational study in Concussion, Mild Traumatic Brain Injury, sponsored by Baylor Research Institute. Terminated at 3 sites in United States. Open to participants aged 8 Years to 99 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-17.

Sponsored by Baylor Research Institute · Observational

Why this study was terminated
PI transitioned to a new institution
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
14
Ages
8 Years to 99 Years
Sex
All
01

Study summary

The goal of this prospective, observational study is to (1) collaborate with our stakeholders to identify essential mTBI-information from existing evidence-based materials to develop a Post-mTBI Educational Resource for children with mTBI and their parents and (2) implement our Post-mTBI Educational Resource into clinical practice to determine feasibility, acceptability, and appropriateness at Baylor Scott and White (BSW) clinical sites that treat children with mTBI.

02

Conditions studied

  • Concussion, Mild Traumatic Brain Injury

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Keywords

  • concussion
  • mTBI
03

In context

Brain Concussion

530 studies on the registry are indexed under Brain Concussion; 151 are open to participants now.

This study's enrollment of 14 is below the median of 180 across 146 observational studies indexed under Brain Concussion.

Browse Brain Concussion studies →

Lead sponsor

Baylor Research Institute is the lead sponsor of 219 studies on the registry; 49 are open to participants now.

Of its 23 completed or terminated interventional studies of FDA-regulated products, 9 (39%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
8 Years to 99 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Potential stakeholders will be between the ages of 8 and 99 years.

Inclusion criteria

  • children and young adults who are student athletes
  • they have experienced a mTBI
  • parents, coaches, and professional stakeholders (e.g., athletic trainers, school nurses, school administrators, physicians, healthcare administrators, local and national entities, community partners).
  • Stakeholders were part of our previous Engagement Award.

Exclusion criteria

Exclusion Criteria:

  • Individuals younger than 8 years old
  • Anyone who does not meet the above criteria
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
14 participants (actual)
Patient registry
No

Groups and cohorts

  • Advisory Board (AB)

    Our target AB of stakeholders include children and young adults who are student athletes and have experienced mTBI, parents, coaches, and professional stakeholders (e.g., athletic trainers, school nurses, school administrators, physicians, healthcare administrators, local and national entities, community partners)

    Other: Post-mTBI Educational Resource

Interventions

  • OtherPost-mTBI Educational Resource

    Activate clinicians and clinic administrators at BSW clinical sites that treat children with mTBI to implement the Post-mTBI Educational Resource.

06

What researchers measure

Primary outcomes

  1. Engagement

    \# of Advisory Board members

    Time frame: through study completion, an average of 3 years

  2. Engagement

    \# of Engagment Partners

    Time frame: through study completion, an average of 3 years

  3. Engagement

    Feedback and Satisfaction on The Patient Engagement in Research Scale (PEIRS). Total scores are calculated on a scale of 0 to 100, where higher scores indicate more meaningful engagement.

    Time frame: through study completion, an average of 3 years

07

Study locations

3 sites
  • BSW Primary Care at The Star
    Frisco, Texas 75034, United States
  • BSW Sports Concussion Program
    Frisco, Texas 75034, United States
  • McLane Children's Hospital at BSW Temple Medical Center
    Temple, Texas 76502, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 17, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07414303
Lead sponsor
Baylor Research Institute
Responsible party
Sponsor
First posted
Feb 17, 2026
Start date
Mar 4, 2025
Primary completion
Dec 8, 2025
Completion
Dec 8, 2025
Last update
Feb 17, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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