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Smart Phone Application for Postconcussion Symptom Reduction

Smart Phone Application for Postconcussion Symptom Reduction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02501642
Enrollment
479
Registered
2015-07-17
Start date
2014-12-01
Completion date
2018-09-30
Last updated
2023-07-28

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

Conditions

Concussion

Brief summary

The proposed study will address a very important issue for the VA both currently and in the future -- the high percentage of OIF/OEF/OND Veterans who have been medically diagnosed with a mild traumatic brain injury (mild TBI) and experience distressing symptoms. Smart phone mobile applications have become a primary source of information and communication among large percentages of Americans, especially those of the OIF/OEF/OND generation. The proposed study is a 4-year randomized control trial investigating the utility of an interactive, self-management smartphone application, TBI Coach, one of a suite of mobile applications developed by VA. The primary goal of the proposed study is to evaluate the efficacy of TBI Coach for improving clinical outcomes in those with a history of mild TBI and to determine what aspects of TBI Coach are most useful to Veterans. An overarching goal of this line of research is to improve access among Veterans with mild TBI who still have symptoms months to years after injury. Objectives. The study will pursue the following objectives: 1. Evaluate the efficacy of TBI coach for improving clinical outcomes among recipients of TBI Coach. 2. Determine the aspects of TBI Coach most associated with positive outcomes. 3. Obtain qualitative information on factors associated with use of TBI coach or with deriving benefit from use of TBI Coach that can be used to inform future modifications of the application and wide scale implementation.

Detailed description

Patients who meet eligibility criteria and consent to participate in the study will be randomly assigned to one of two arms, either the Concussion Coach group, which will receive an iPod touch® with the Concussion Coach Explorer version, or into the no mobile app control group. Study personnel will explain the purpose of the study, complete the informed consent process, obtain the random treatment assignment from a randomization sheet, and introduce the participant to his/her baseline evaluator. The random assignment to intervention will be accomplished in blocks within each site. While small block sizes allow intervention group sizes to be very similar it may make the allocation process predictable. Therefore to reduce selection bias and achieve balance across the intervention arms sequence list of individual assignments by random block sizes will be generated. Both groups will be assessed in a pre/post intervention design and will be compensated for their time completing study surveys. During the 3 months that they are involved in the study, the intervention group will be sent (via Concussion Coach) reminders to engage with the app on a weekly basis. Their use (e.g., total time spent on each component of the app) will be collected electronically. Both groups will receive care as usual (meaning their regularly scheduled VA appointments and medications). At the completion of the study, both groups will be encouraged to download the App for their own use, with assistance from the study team if needed. Description of Intervention & Training The Concussion Coach is designed to provide psychoeducation, self-assessment, and treatment of PCS symptoms following a mild TBI. The PI and three of the co-investigators were co-developers of Concussion Coach. The public-facing Concussion Coach will be available for free download from a public marketplace and available for use with most mobile devices. The application has the advantage of privacy and anonymity, thus addressing the stigma often expressed as a barrier to seeking treatment. A mirror version of the public version, called Concussion Coach Explorer Version, will be developed within three months and used for this study. Unlike the public version, it will have the capacity to collect usage information, such as length of time spent on each part of the app, self-report ratings of symptoms and distress, and identification of favorites among the self-help tools. These data can be uploaded in a de-identified form to a HIPAA compliant server. Other than the ability to collect data, it will be exactly like the real Concussion Coach. The Explorer version will be developed by our collaborators, Vertical Product Development, which developed Concussion Coach, PTSD Coach, and PTSD Explorer version. Explorer versions are especially useful as they allow for unobtrusive, highly detailed, real-time data collection without relying on patient self-report. In addition, the Concussion Coach will be an 'opportunistic' exporter of data. It will upload data to the server whenever it has new data and is in a WiFi zone; participants do not have to have a home wireless network. If they never enter a WiFi area, the investigators will collect their data at study termination when the investigators collect the iPod touch®. The investigators will utilize ohmage, an existing open source technology stack, to port the app to the server.

Interventions

BEHAVIORALConcussion Coach

smart phone app with educational material on postconcussion symptoms and behavioral self-monitoring/strategies

OTHERTreatment as usual

Treatment as usual

Sponsors

VA Office of Research and Development
Lead SponsorFED

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* 18 or older * History of mild TBI (DoD/VA) as determined by trained, experienced staff via interview and medical record review via comprehensive evaluation process within PNS with current symptoms complaints operationally defined as at least two symptoms on the NSI endorsed at the 'moderate' level or a total score on the NSI greater than 25 * Must speak and read English * Not have a history of moderate to severe TBI * Not have a self-reported diagnosis of psychosis or be actively suicidal

Exclusion criteria

* Subjects who report prior experience with Concussion Coach will also be excluded

Design outcomes

Primary

MeasureTime frameDescription
Neurobehavioral Symptom Inventory3 monthsThe Neurobehavioral Symptom Inventory is a 22-item questionnaire developed to evaluate post-concussive symptom severity following mild TBI (Cicerone and Kalmar 1995). Participants are asked to rate each symptom on a scale of 0-4 (None, Mild, Moderate, Severe, Very Severe) with three different categories of symptoms: Affective/psychological/stress, somatic/physical and cognitive (reflecting three factors). Scores can range from 0-88, with higher scores indicating more severe symptom endorsement.

Countries

United States

Participant flow

Recruitment details

Enrollment closed on 9.30.2018

Pre-assignment details

Enrollment closed on 9.30.2018 N/A

Participants by arm

ArmCount
Concussion Coach Group
After informed consent and randomization, participants will complete baseline study measures and will receive an iPod touch® with the Concussion Coach Explorer version Concussion Coach: smart phone app with educational material on postconcussion symptoms and behavioral self-monitoring/strategies
238
Treatment as Usual
Treatment as usual: Treatment as usual
241
Total479

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up711

Baseline characteristics

CharacteristicTreatment as UsualTotalConcussion Coach Group
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
0 Participants0 Participants0 Participants
Age, Categorical
Between 18 and 65 years
241 Participants479 Participants238 Participants
Age, Continuous35 years
STANDARD_DEVIATION 15
35.5 years
STANDARD_DEVIATION 15.5
36 years
STANDARD_DEVIATION 16
Race (NIH/OMB)
American Indian or Alaska Native
1 Participants3 Participants2 Participants
Race (NIH/OMB)
Asian
1 Participants4 Participants3 Participants
Race (NIH/OMB)
Black or African American
41 Participants78 Participants37 Participants
Race (NIH/OMB)
More than one race
1 Participants2 Participants1 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
13 Participants15 Participants2 Participants
Race (NIH/OMB)
Unknown or Not Reported
13 Participants23 Participants10 Participants
Race (NIH/OMB)
White
171 Participants354 Participants183 Participants
Region of Enrollment
United States
241 Participants479 Participants238 Participants
Sex: Female, Male
Female
21 Participants42 Participants21 Participants
Sex: Female, Male
Male
207 Participants416 Participants209 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 2380 / 241
other
Total, other adverse events
0 / 2380 / 241
serious
Total, serious adverse events
0 / 2380 / 241

Outcome results

Primary

Neurobehavioral Symptom Inventory

The Neurobehavioral Symptom Inventory is a 22-item questionnaire developed to evaluate post-concussive symptom severity following mild TBI (Cicerone and Kalmar 1995). Participants are asked to rate each symptom on a scale of 0-4 (None, Mild, Moderate, Severe, Very Severe) with three different categories of symptoms: Affective/psychological/stress, somatic/physical and cognitive (reflecting three factors). Scores can range from 0-88, with higher scores indicating more severe symptom endorsement.

Time frame: 3 months

ArmMeasureValue (MEAN)Dispersion
Concussion Coach GroupNeurobehavioral Symptom Inventory33 score on a scaleStandard Deviation 16
Treatment as UsualNeurobehavioral Symptom Inventory33 score on a scaleStandard Deviation 17

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