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Australian University of California San Francisco (UCSF) Concussion in Athletes (AUSSIE-2)

Australian UCSF Concussion in Athletes Studied With Cranial Accelerometry Part 2

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05771051
Acronym
AUSSIE-2
Enrollment
68
Registered
2023-03-16
Start date
2022-03-01
Completion date
2022-10-01
Last updated
2023-03-16

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

Conditions

Concussion, Mild

Keywords

headpulse, mTBI

Brief summary

Analysis of cardiac induced brain forces using cranial accelerometry has been shown to diagnose concussion in high school athletes. This trial expands on this observation by recording headpulse signals in a recently concussed athletes playing Australian rules football.

Detailed description

Recently concussed athletes will have headpulse measurements obtained as soon after the clinically identified concussion as is feasible and at 1-3 day intervals over the course of a month. These recordings will pair with a self administered neurological symptom inventory (NSI) to track the athletes subjective concussion symptoms. Data from the prior study (AUSSIE-1) will be used to confirm the predictive value of the established algorithm

Interventions

Placement of headset on subject

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Concussion Subjects: Inclusion Criteria: * Diagnosed with sport related concussion * first recording obtained within one week * willingness to have multiple recordings in the month following concussion Exclusions: \- head laceration Control subjects: Inclusion Criteria * athletes without concussion over the last year * willingness to have single or multiple recordings

Exclusion criteria

* head laceration

Design outcomes

Primary

MeasureTime frameDescription
Accuracy of model for the detection of concussion1 monthSensitivity of headpulse measurements confirming concussion

Secondary

MeasureTime frameDescription
Time to recovery of headpulse following concussion1 MonthTime (hours) when the headpulse biometric returns to within 1 SD of normal values

Countries

United States

Outcome results

None listed

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