Concussion, Mild Traumatic Brain InjuryPOCKITNCT07414303
Implementation of an Evidence-Based Educational Resource for Children With Mild Traumatic Brain Injury
An observational study of Concussion, Mild Traumatic Brain Injury, run by Baylor Research Institute at 3 sites in United States.
Trial 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… Read more about this study
- Who is it for?
- Ages 8 to 99 yearsHealthy volunteers can take part
- Conditions the study is for
- Concussion, Mild Traumatic Brain Injury
- What is being tested?
- Post-mTBI Educational Resource
- How many people
- 14 participants
- Where
- 3 sitesUnited States
- Study dates
- 4 Mar 2025to 8 Dec 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 8 to 99 years
- All sexes
- Healthy volunteers accepted
- Child, Adult, Older adult
Study population: Potential stakeholders will be between the ages of 8 and 99 years.
Who may be able to join
- 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.
Who cannot join
- Individuals younger than 8 years old
- Anyone who does not meet the above criteria
Trial locations and contacts
3 sites in 1 country.
United States3 sites
BSW Primary Care at The Star
Frisco, Texas, 75034
BSW Sports Concussion Program
Frisco, Texas, 75034
McLane Children's Hospital at BSW Temple Medical Center
Temple, Texas, 76502
About this study
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.
- Conditions
- Concussion, Mild Traumatic Brain Injury
- Being tested
- Post-mTBI Educational Resource
- Keywords
- concussion, mTBI
- Medical subject headings
- Brain Concussion
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Post-mTBI Educational ResourceOther
Activate clinicians and clinic administrators at BSW clinical sites that treat children with mTBI to implement the Post-mTBI Educational Resource.
| Study group | Role | What they receive |
|---|---|---|
| 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) Receives: Other: Post-mTBI Educational Resource |
What is being measured
The primary outcome is the main question the study is designed to answer.
Engagement
# of Advisory Board members
Measured: through study completion, an average of 3 years
Engagement
# of Engagment Partners
Measured: through study completion, an average of 3 years
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.
Measured: through study completion, an average of 3 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Feb 2026
- Study start4 Mar 2025
- Primary completion8 Dec 2025
- Study completion8 Dec 2025
Why it stopped: PI transitioned to a new institution
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Concussion, Mild Traumatic Brain InjuryStudies of the same condition, open and under way.
- More trials run by Baylor Research InstituteThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 14 participants (actual)
Sponsor and investigators
- Lead sponsor
- Baylor Research Institute
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07414303
- Sponsor's protocol ID
- 90IFDV0035
- Acronym
- POCKIT
- Status last verified
- Feb 2026
- First submitted
- 3 Mar 2025
- Last updated
- 17 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 17 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Implementation of an Evidence-Based Educational Resource for Children With Mild Traumatic Brain Injury
- ClinicalTrials.gov ID
- NCT07414303
- Acronym / sponsor ID
- POCKIT / 90IFDV0035
- Conditions
- Concussion, Mild Traumatic Brain Injury
- Keywords
- concussion, mTBI
- Study type
- Observational
- Recruitment status
- TerminatedReason stopped: PI transitioned to a new institution
- Enrolment
- 14 participants (actual)
- Lead sponsor
- Baylor Research InstituteUniversity, hospital or other
- Study start
- 4 Mar 2025 (actual)
- Primary completion
- 8 Dec 2025 (actual)
- Study completion
- 8 Dec 2025 (actual)
- First posted
- 17 Feb 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Advisory Board (AB) | – | Other: Post-mTBI Educational ResourceOur 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) |
Who may qualify
- Ages
- 8 to 99 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult, Older adult
- Study population
- Potential stakeholders will be between the ages of 8 and 99 years.
Key inclusion criteria (4 listed)
- 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.
Key exclusion criteria (2 listed)
- Individuals younger than 8 years old
- Anyone who does not meet the above criteria
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Post-mTBI Educational ResourceActivate clinicians and clinic administrators at BSW clinical sites that treat children with mTBI to implement the Post-mTBI Educational Resource. | Other | Advisory Board (AB) |
Primary outcome
Engagement
Time frame: through study completion, an average of 3 years
# of Advisory Board members
Engagement
Time frame: through study completion, an average of 3 years
# of Engagment Partners
Engagement
Time frame: through study completion, an average of 3 years
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.
Results and safety
The study was stopped early (reason given: PI transitioned to a new institution). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Feb 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Concussion, Mild Traumatic Brain Injury, run by Baylor Research Institute at 3 sites in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 17 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study was stopped early (reason given: PI transitioned to a new institution). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Engagement (time frame: through study completion, an average of 3 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Feb 2026.