Field Implementation of iDETECT

March 3, 2016 updated by: Tamara Espinoza, MD, Emory University

Implementation of iDETECT for Field Triage of mTBI in Football Players

The purpose of this study is to assess a new screening tool for sideline evaluation of concussion injuries in athletes. iDETECT is a new technology that combines several elements of recommended concussion screening tools into a single, portable device.

Study Overview

Detailed Description

The goal of the research is to evaluate the use of a multimodal platform (iDETECT) for immediate post-injury neuropsychological, balance and oculomotor assessment, and to evaluate the iDETECT platform as a return-to-play assessment tool during the post injury management period following concussion.

Study Type

Observational

Enrollment (Actual)

124

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Georgia
      • Atlanta, Georgia, United States, 30327
        • Westminster High School
      • College Park, Georgia, United States, 30337
        • Woodward Academy
      • Marietta, Georgia, United States, 30064
        • Marietta High School
      • Roswell, Georgia, United States, 30075
        • Blessed Trinity Catholic High School

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

iDETECT will be used to assess neuro-functional outcomes known to be impaired after mTBI in competitive high school athletic teams over a standard season.

Eligible participants include: a) all football athletes at participating high schools; b) all non-football athletes who sustain a concussion during the Fall 2015 season; c) interested non-collision sport athletes without a concussion (to serve at controls).

Description

Inclusion Criteria:

  • Athletes participating in the Fall 2015 high school season
  • Aged 14 years or older
  • No concussion injuries within prior 2 months
  • Provide signed and data consent and/or assent form(s)

Exclusion Criteria:

  • Non-English speaking
  • History of seizures or prior brain surgery (excluding facial and TM surgery)
  • Concussion within last 2 months
  • Poor Effort on baseline iDETECT test

Non-Collision Sport Group

  • current concussion or history of current concussion during the Fall 2015 athletic season

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Football Athlete Group

All football athlete participants in this arm will take the integrated Display Enhanced Testing for Cognitive Impairment and mild traumatic brain injury (iDETECT) test. Participants who sustain a concussion during the football season will complete the iDETECT test and a standing balance test (BESS assessment) four times after injury. Participants in this arm are eligible to receive the Riddell High Impact Technology (HIT) System or the i1 Biometrics Vector Mouth Guard.

NOTE: Football athletes who sustain a concussion during the football season will be evaluated and managed according to standard concussion screening and return-to-play (RTP) protocols. Performance on iDETECT or other study related tasks will NOT be used to make diagnosis, management, or return to play decisions. Study staff will not assist with or influence diagnosis, management, or return-to-play decision making by teams' medical personnel.

iDETECT offers an open platform for an evaluation of cognitive, balance, and oculomotor performance after mild traumatic brain injury (mTBI). It is a rugged, portable, neurocognitive assessment tool designed specifically for use in field and triage settings for the rapid evaluation of functional neurologic impairment after potential concussive injury.
The Riddell HIT system incorporates six acceleration sensors into standard football helmets worn during practice and game play. A computerized sideline system captures information on linear and rotational acceleration, as well as magnitude, duration, and location of impact for each player
The i1 Biometrics Vector Mouth Guard is an impact intelligence system that contains a collection of impact sensing mouth guards, housing accelerometer and gyroscope technology that allows real-time collection and storage of biomechanical impact data. Sensors in the mouth guard communicate directly with a sideline assessment base station and allows for immediate assessment and evaluation of hit exposure.
Non-Collision Sport Athlete Group

Non-collision sport athletes who are active in a school's Fall athletic program will be take the integrated Display Enhanced Testing for Cognitive Impairment and mild traumatic brain injury (iDETECT) test, standing balance test (BESS assessment), and complete a questionnaire at the beginning of the sport season. Participants will be asked to take the iDETCT test up to 5 more times during the season. Participants who sustain a concussion during the athletic season will be asked to take additional iDETECT tests four times after the injury.

NOTE: Non-collision sport athletes who sustain a concussion during the season will be evaluated and managed according to standard concussion screening and return-to-play (RTP) protocols. Performance on iDETECT or other study related tasks will NOT be used to make diagnosis, management, or return to play decisions. Study staff will not assist with or influence diagnosis, management, or return-to-play decision making by teams' medical personnel.

iDETECT offers an open platform for an evaluation of cognitive, balance, and oculomotor performance after mild traumatic brain injury (mTBI). It is a rugged, portable, neurocognitive assessment tool designed specifically for use in field and triage settings for the rapid evaluation of functional neurologic impairment after potential concussive injury.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Area under the curve (AUC) for iDetect total score of neuropsychological assessment (NP) compared to the trainer's determination of clinical concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for total score of NP will be computed and compared with the trainer's determination of clinical concussion to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDetect NP total score compared to the Immediate Post-Concussion Assessment and Cognitive Testing (ImPACT) score
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for total score of NP will be computed and compared to the ImPACT score to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDetect NP response time to stimuli compared to the trainer's determination of clinical concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for NP response will be computed and compared trainer's determination of clinical concussion to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDetect NP response time to stimuli compared to Immediate Post-Concussion Assessment and Cognitive Testing (ImPACT) score
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for NP response will be computed and compared the ImPACT score to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT total score compared to final clinical determination of concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for iDETECT total score will be compared to the trainer's final clinical determination of concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT total score compared to the Sport Concussion Assessment Tool (SCAT3)
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for iDETECT total score will be compared to the SCAT 3 score. SCAT3 is a standardized tool for evaluating injured athletes for concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Area under the curve (AUC) for iDETECT Non-postural Balance/Sensory Integration (SI) battery time to balance compared to trainer's determination of clinical concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for SI battery time will be computed and compared to the trainer's determination of clinical concussion to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Non-postural Balance/Sensory Integration (SI) battery time to balance compared to Balance Error Scoring System (BESS) score
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for SI battery time will be computed and compared to BESS score to find out if iDETECT is as accurate in diagnosing concussion.The SI battery requires participants to utilize primary sensory inputs to assess the state of a virtual balance beam displayed within the iDETECT visor immersive environment without standing.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Non-postural Balance/Sensory Integration (SI) battery number of overshoots compared to BESS score
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for SI battery number of overshoots will be computed and compared to the BESS score to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Vestibular and Oculomotor (VO) battery angle difference in target motion prediction compared to trainer's determination of clinical concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for VO battery angle distance in target motion prediction will be computed and compared to the trainer's determination of clinical concussion to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Vestibular and Oculomotor (VO) battery angle difference in target motion prediction compared to King-Devick score (time and number of errors)
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) will be computed and compared to the King-Devick score (time and number of errors).
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Vestibular and Oculomotor (VO) battery angle difference in target motion interefence compared to trainer's determination of clinical concussion
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for VO battery angle difference in target motion interference will be computed and compared to the trainer's determination of clinical concussion to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Area under the curve (AUC) for iDETECT Vestibular and Oculomotor (VO) battery angle difference in target motion interefence compared to King-Devick score (time and number of errors)
Time Frame: Baseline, throughout duration of sport season (an expected average of 4 months)
The area under the receiver operator characteristic (ROC) curve (the concordance index) for VO battery angle difference in target motion interference will be computed and compared to the to King-Devick score (time and number of errors) to find out if iDETECT is as accurate in diagnosing concussion.
Baseline, throughout duration of sport season (an expected average of 4 months)
Change in iDETECT total score from baseline to time of injury
Time Frame: Baseline, time of concussion
Difference in iDETECT total score from baseline to time of concussion will be used to calculate the degree of discrimination in concussed athletes.
Baseline, time of concussion
Change in iDETECT total score from baseline to end of season to assess subconcussion
Time Frame: Baseline, end of sport season (an expected average of 4 months)
Mean scores between cases and controls will be compared on iDETECT. Change is defined as the difference in scores from baseline to the end of the season.
Baseline, end of sport season (an expected average of 4 months)
Change in Sport Concussion Assessment Tool 3 (SCAT3) total score from baseline to end of season to assess subconcussion
Time Frame: Baseline, end of sport season (an expected average of 4 months)
Mean scores between cases and controls will be compared using the SCAT3. Change is defined as the difference in scores from baseline to the end of the season.
Baseline, end of sport season (an expected average of 4 months)
iDETECT word recall score post injury
Time Frame: 3 days post injury (3 minutes)
Subjects are asked to remember a group of 12 words displayed one at a time. They are then shown 24 words and asked to respond 'YES' for a word in the original list and 'NO' for a word that was not in the original list. Subjects are scored on the number of words they correctly remember being on the list.
3 days post injury (3 minutes)
Change in iDETECT mean word recall score post injury, 10 days
Time Frame: 3 days post injury (3 minutes), 10 days post injury (3 minutes)
Subjects are asked to remember a group of 12 words displayed one at a time. They are then shown 24 words and asked to respond 'YES' for a word in the original list and 'NO' for a word that was not in the original list. Subjects are scored on the number of words they correctly remember being on the list. Change is defined as the difference in scores from 3 days post injury to 10 days post injury.
3 days post injury (3 minutes), 10 days post injury (3 minutes)
Change in iDETECT mean word recall score post injury, 30 days
Time Frame: 10 days post injury (3 minutes), 30 days post injury (3 minutes)
Subjects are asked to remember a group of 12 words displayed one at a time. They are then shown 24 words and asked to respond 'YES' for a word in the original list and 'NO' for a word that was not in the original list. Subjects are scored on the number of words they correctly remember being on the list. Change is defined as the difference in scores from 10 days post injury to 30 days post injury.
10 days post injury (3 minutes), 30 days post injury (3 minutes)
iDETECT shapes test score post injury
Time Frame: 3 days post injury (2 minutes)
Subjects are presented a shape stimulus with 3 characteristics: shape, color, and crosshatch orientation and asked to remember the object. The subject selects the correct shape with 'YES' and each incorrect shape with 'NO'. Score is calculated by correctly selecting the shape.
3 days post injury (2 minutes)
Change in iDETECT mean shapes test score post injury, 10 days
Time Frame: 3 days post injury (2 minutes), 10 days post injury (2 minutes)
Subjects are presented a shape stimulus with 3 characteristics: shape, color, and crosshatch orientation and asked to remember the object. The subject selects the correct shape with 'YES' and each incorrect shape with 'NO'. Score is calculated by correctly selecting the shape. Change is defined as the difference in scores from 3 days post injury to 10 days post injury.
3 days post injury (2 minutes), 10 days post injury (2 minutes)
Change in iDETECT mean shapes test score post injury, 30 days
Time Frame: 10 days post injury (3 minutes), 30 days post injury (3 minutes)
Subjects are presented a shape stimulus with 3 characteristics: shape, color, and crosshatch orientation and asked to remember the object. The subject selects the correct shape with 'YES' and each incorrect shape with 'NO'. Score is calculated by correctly selecting the shape. Change is defined as the difference in scores from 10 days post injury to 30 days post injury.
10 days post injury (3 minutes), 30 days post injury (3 minutes)
iDETECT arrows test score post injury
Time Frame: 3 days post injury (2 minutes)
Subjects are asked to respond to an arrow with 2 characteristics: orientation and color. If the arrow is blue, they select the side that the arrow is pointing. If the arrow is red, they select the side opposite from where it is pointing. Score is calculated by the number of correct responses.
3 days post injury (2 minutes)
Change in iDETECT mean arrows test score post injury, 10 days
Time Frame: 3 days post injury (2 minutes), 10 days post injury (2 minutes)
Subjects are asked to respond to an arrow with 2 characteristics: orientation and color. If the arrow is blue, they select the side that the arrow is pointing. If the arrow is red, they select the side opposite from where it is pointing. Score is calculated by the number of correct responses. Change is defined as the difference in scores from 3 days post injury to 10 days post injury.
3 days post injury (2 minutes), 10 days post injury (2 minutes)
Change in iDETECT mean arrows test score post injury, 30 days
Time Frame: 10 days post injury (2 minutes), 30 days post injury (2 minutes)
Subjects are asked to respond to an arrow with 2 characteristics: orientation and color. If the arrow is blue, they select the side that the arrow is pointing. If the arrow is red, they select the side opposite from where it is pointing. Score is calculated by the number of correct responses. Change is defined as the difference in scores from 10 days post injury to 30 days post injury.
10 days post injury (2 minutes), 30 days post injury (2 minutes)
iDETECT N-BACK (1-back and 2-back) test post injury
Time Frame: 3 days post injury (2 minutes)
Subjects view a series of faces one at a time and choose if the face has been shown before. The subject selects 'YES' if the face shown is the same as the previous or 'NO' if it is not. Score is calculated by the number of correct responses.
3 days post injury (2 minutes)
iDETECT Delayed Word Recall Test
Time Frame: 3 days post injury (2 minutes)
Subjects are asked to recite words from the word recall test after a five minute delay. Score is calculated by the number of words correctly recalled.
3 days post injury (2 minutes)
Change in iDETECT Delayed Word Recall Test
Time Frame: 3 days post injury (2 minutes), 10 days post injury (2 minutes)
Subjects are asked to recite words from the word recall test after a five minute delay. Score is calculated by the number of words correctly recalled. Change is defined as the difference in scores from 3 days post injury to 10 days post injury.
3 days post injury (2 minutes), 10 days post injury (2 minutes)
Change in iDETECT Delayed Word Recall Test
Time Frame: 10 days post injury (2 minutes), 30 days post injury (2 minutes)
Subjects are asked to recite words from the word recall test after a five minute delay. Score is calculated by the number of words correctly recalled. Change is defined as the difference in scores from 10 days post injury to 30 days post injury.
10 days post injury (2 minutes), 30 days post injury (2 minutes)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Collaborators

Investigators

  • Principal Investigator: Tamara Espinoza, MD, MPH, Emory University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2015

Primary Completion (Actual)

February 1, 2016

Study Completion (Actual)

February 1, 2016

Study Registration Dates

First Submitted

August 19, 2015

First Submitted That Met QC Criteria

August 19, 2015

First Posted (Estimate)

August 20, 2015

Study Record Updates

Last Update Posted (Estimate)

March 4, 2016

Last Update Submitted That Met QC Criteria

March 3, 2016

Last Verified

March 1, 2016

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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