NCT07129577

Brief Summary

Traumatic brain injury (TBI) is estimated to have the highest incidence of all common neurological disorders, affecting 50 to 60 million people worldwide each year. In the UK, approximately one million people attend an Emergency Department (ED) annually following a head injury, and 80-90% of these are classified as mild TBI (mTBI), also referred to as concussion. In the acute setting, mTBI is typically defined by a Glasgow Coma Scale (GCS) score of 13-15 on presentation. Current acute management focuses primarily on identifying which patients require a CT head scan to detect life threatening injuries that may need neurosurgical intervention, observation, or neurocritical care. However, there is increasing recognition that the term "mild" can be misleading. Many patients, including those with normal CT scans,experience persistent functional, cognitive, and symptomatic deficits that may benefit from further intervention and follow-up care. Blood biomarkers offer significant potential to improve the early diagnosis, risk stratification, and prognostication of mTBI in the ED setting. While these biomarkers are increasingly being developed and evaluated in moderate and severe TBI, their clinical utility in mild TBI has not yet been definitively demonstrated. To fully assess their potential value, it is essential to understand the current care pathways for mTBI in the ED, how they are implemented in practice, and where biomarker information could meaningfully enhance clinical decision making and improve patient outcomes. The POCKET study will use a systems engineering approach, in combination with health economic evaluation, to assess the potential role and utility of point-of-care blood biomarkers in the management of mild TBI in UK emergency departments. This research will be conducted using the Abbott biomarker platform.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
400

participants targeted

Target at P75+ for all trials

Timeline
4mo left

Started Sep 2025

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress69%
Sep 2025Aug 2026

First Submitted

Initial submission to the registry

August 12, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

August 19, 2025

Completed
13 days until next milestone

Study Start

First participant enrolled

September 1, 2025

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 29, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 29, 2026

Last Updated

August 19, 2025

Status Verified

August 1, 2025

Enrollment Period

12 months

First QC Date

August 12, 2025

Last Update Submit

August 12, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Understanding of the current clinical pathway and how use of point of care biomarkers may change this.

    From enrolment to 6 months

Eligibility Criteria

Age18 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients who present to Emergency Departments (EDs) with mild traumatic brain injury (mTBI) defined as Glasgow Coma Score \>12.

You may qualify if:

  • Adult patients (≥ 18 years of age)
  • Glasgow Coma Score \>12
  • Presentation within 24 hours of head injury
  • Meet criteria to be assessed using NICE NG232 clinical decision support tool (CDST).
  • Patients with a prior history of TBI may still be included.

You may not qualify if:

  • Participant without capacity and no available patient legal representative or professional consultee.
  • Participant with capacity unwilling to provide informed consent
  • Unable to adequately understand written and verbal English.
  • Prisoners currently in custody of HM Prison Service

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Craniocerebral TraumaBrain Injuries, Traumatic

Condition Hierarchy (Ancestors)

Trauma, Nervous SystemNervous System DiseasesWounds and InjuriesBrain InjuriesBrain DiseasesCentral Nervous System Diseases

Central Study Contacts

POCkET Study Coordinator

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Honorary Consultant in Critical Care and Emergency Medicine / Clinician Scientist Fellow

Study Record Dates

First Submitted

August 12, 2025

First Posted

August 19, 2025

Study Start

September 1, 2025

Primary Completion (Estimated)

August 29, 2026

Study Completion (Estimated)

August 29, 2026

Last Updated

August 19, 2025

Record last verified: 2025-08