Development of a Concussion Management Platform for Children and Youth (Back2PlayApp)
Primary Purpose
Concussion, Brain
Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Back2Play App
Sponsored by
About this trial
This is an interventional treatment trial for Concussion, Brain focused on measuring youth or children, mHealth
Eligibility Criteria
Inclusion Criteria:
- diagnosed concussion
- symptomatic
- within 4 weeks of diagnosis
Exclusion Criteria:
- developmental delay
- significant brain injury requiring resuscitation, admission to PCCU or surgical intervention
- multisystem injury
Sites / Locations
- McMaster Children's HospitalRecruiting
- Montreal Children's HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
App group
Usual Care
Arm Description
Participants will use the Back2Play App to support them in following the guidelines for recovery from concussion
Participants will receive usual care which often means they are provided concussion recovery guidelines in handout format and receive whatever follow up is deemed necessary by treating physician
Outcomes
Primary Outcome Measures
Rate of re-injury
Survey-report on whether another concussion has occurred. Yes/No response
Change in number and severity of Post-concussive symptoms (PCSS)
Daily surveys of 22 concussion symptoms (1symptom/0 no symptoms) for # of symptoms. Included in these surveys is report of symptom changes (gone, better, same or worst) that will help to evaluate changes by stage of recovery and over the course of recovery.
Secondary Outcome Measures
Time to recovery from concussion
Measurement of time from injury to when youth have recovered (return to activity stage 6/return to school stage 5)
System Usability Scale (SUS) (for the App group only)
10 item questionnaire using a Likert scale with five response options for measuring usability of a system (App) 1=strongly disagree 5= strongly agree; Scores are converted to an overall percentage with 70% and above a good score
Full Information
NCT ID
NCT05471791
First Posted
April 14, 2022
Last Updated
February 28, 2023
Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR), Natural Sciences and Engineering Research Council, Canada, McMaster Children's Hospital, Montreal Children's Hospital of the MUHC, Hamilton-Wentworth Catholic District School Board
1. Study Identification
Unique Protocol Identification Number
NCT05471791
Brief Title
Development of a Concussion Management Platform for Children and Youth
Acronym
Back2PlayApp
Official Title
Development of a Concussion Management Platform for Children and Youth: Bridging the Gap Between Research and Practice
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 6, 2022 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR), Natural Sciences and Engineering Research Council, Canada, McMaster Children's Hospital, Montreal Children's Hospital of the MUHC, Hamilton-Wentworth Catholic District School Board
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This multi-centred, randomized controlled trial will evaluate the effectiveness of a pilot tested mobile device Application built to guide youth in recovery from concussion. The Back2Play App was developed based on the published and researched CanChild Return to Activity (RTA) and Return to School (RTS) guidelines, which outline graduated steps in returning to play and school for youth after a concussion. It is hypothesized that participants who use the App will have better outcomes from concussion, primarily less reinjury during the vulnerable period throughout their recover up to 3- 6 months after concussion. They may also experience reduced frequency and severity of symptoms and recover more quickly from their concussion.
Detailed Description
Children 10- 18 years of age will be recruited from Emergency departments in Hamilton, Ontario and Montreal, Quebec as well as from community physicians, school boards and sporting organizations. All participants will be randomized to either the App (intervention) group or to Usual care (control) group.
Those in the App group will be loaned an Apple watch (and iPhone if they don't have one). The App is designed to monitor self-reported symptoms and stages of recovery and combine these results with their activity and heart rate data collected by the watch. Notifications are sent through the App based on this data that may help youth adhere to the Return to Activity and Return to School (RTA/RTS) guidelines. Participants will fill out symptom surveys in the App up to 3 times daily, record their physical and cognitive activities and assign themselves a stage of recovery; RTA 1-6, RTS 1-5. The homepage of the App reminds them of what stage they are in of RTA and RTS as well as how much light, moderate and vigorous activity is encouraged for their individual stage of recovery. They will receive notifications about activity level and heart rate if these go outside the recommended limits. App users will also receive motivational statements and encouragement.
Participants will by directed by the Back2Play App to a companion App called Braingames triggered by recording progress in their stage of returning to school. The Braingames App is a cognitive screen made up of 5 neuro-cognitive tests; 1) Finger tapping, 2) Divided Attention, 3) Memory for Designs, 4) Path tracing and 5) Face emotion matching. These tasks appear to be particularly sensitive in detecting deficits post-concussion. The tasks are in a game format on the App and responses are collected and feedback provided to the youth as to their readiness to progress to greater cognitive challenges by demonstrating that If these tests provoke more symptoms, participants may want to consider if they are ready to move up a stage in return to school.
The control group will receive usual care with the approach provided in health care systems in their community. This often involves a handout with some type of graduated rest and return to play advice. These participants will complete the initial Post Concussion Symptom Scale at their entry into the study and will be sent daily symptom and activity surveys by our secure data capture system (REDCap) to complete. They will also be asked to self-select their stage of concussion recovery daily for both activity and school.
All participants will be scheduled for a zoom interview after their symptoms are gone, or 3 months after enrolling for those who do not achieve full recovery during the study. They will be asked questions about: 1) their understanding and experience with concussion recovery, 2) whether they experienced another head injury and 3) if those who used the App liked it and found it helpful. 3 months after study completion, participants will receive another survey asking if they have experienced any additional head injuries. Those using the App will be given the System Usability Scale (SUS) to objectively rate the App for potential future commercialization.
All data will be analyzed as discussed in the study protocol. Data may also be used fill in the architecture of a machine learning algorithm running in the background of the Back2Play App to use in predicting RTA/RTS stages for participants in future iterations of the App.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Concussion, Brain
Keywords
youth or children, mHealth
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized control trial comparing treatment (use of mobile App) to usual care
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
App group
Arm Type
Experimental
Arm Description
Participants will use the Back2Play App to support them in following the guidelines for recovery from concussion
Arm Title
Usual Care
Arm Type
No Intervention
Arm Description
Participants will receive usual care which often means they are provided concussion recovery guidelines in handout format and receive whatever follow up is deemed necessary by treating physician
Intervention Type
Device
Intervention Name(s)
Back2Play App
Intervention Description
This App uses the Apple watch to monitor activity level and heart rate and combines this with self reported symptoms and stage of recovery to send notifications, suggestions and provide resources to help participants adhere to the guidelines.
Primary Outcome Measure Information:
Title
Rate of re-injury
Description
Survey-report on whether another concussion has occurred. Yes/No response
Time Frame
Surveyed 3 months after completion of study (6 months maximum from enrollment)
Title
Change in number and severity of Post-concussive symptoms (PCSS)
Description
Daily surveys of 22 concussion symptoms (1symptom/0 no symptoms) for # of symptoms. Included in these surveys is report of symptom changes (gone, better, same or worst) that will help to evaluate changes by stage of recovery and over the course of recovery.
Time Frame
Throughout the study until recovered or up to a maximum of 3 months after enrolment
Secondary Outcome Measure Information:
Title
Time to recovery from concussion
Description
Measurement of time from injury to when youth have recovered (return to activity stage 6/return to school stage 5)
Time Frame
Through study completion, an average of 1 month, up to 6 months post-enrollment
Title
System Usability Scale (SUS) (for the App group only)
Description
10 item questionnaire using a Likert scale with five response options for measuring usability of a system (App) 1=strongly disagree 5= strongly agree; Scores are converted to an overall percentage with 70% and above a good score
Time Frame
upon completion of study (max 3 months post enrollment)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
10 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
diagnosed concussion
symptomatic
within 4 weeks of diagnosis
Exclusion Criteria:
developmental delay
significant brain injury requiring resuscitation, admission to PCCU or surgical intervention
multisystem injury
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Kathy Stazyk, MSc
Phone
289-208-1139
Email
stazyk@mcmaster.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Samantha Perrotta, MPH
Phone
365-366-5620
Email
perros2@mcmaster.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carol A DeMatteo, MSc
Organizational Affiliation
McMaster University FHS
Official's Role
Principal Investigator
Facility Information:
Facility Name
McMaster Children's Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 3Z5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Redjana Carciumaru, MSc
Phone
905-521-2100
Email
carcir@mcmaster.ca
Facility Name
Montreal Children's Hospital
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3Z 1X3
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joanna Mazza
Email
joanna.mazza@muhc.mcgill.ca
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
The plan is to share all IPD that underlie results in a publication.
IPD Sharing Time Frame
Data will be available 9 months and ending 36 months after article publication.
IPD Sharing Access Criteria
Proposals for data analysis will be considered if there is a methodologically sound request. All requests should go through the PI dematteo@mcmaster.ca
Citations:
PubMed Identifier
31876794
Citation
DeMatteo CA, Lin CA, Foster G, Giglia L, Thabane L, Claridge E, Noseworthy MD, Hall GB, Connolly JF. Evaluating Adherence to Return to School and Activity Protocols in Children After Concussion. Clin J Sport Med. 2021 Nov 1;31(6):e406-e413. doi: 10.1097/JSM.0000000000000800.
Results Reference
background
PubMed Identifier
32153982
Citation
DeMatteo C, Bednar ED, Randall S, Falla K. Effectiveness of return to activity and return to school protocols for children postconcussion: a systematic review. BMJ Open Sport Exerc Med. 2020 Feb 24;6(1):e000667. doi: 10.1136/bmjsem-2019-000667. eCollection 2020.
Results Reference
background
PubMed Identifier
31625406
Citation
DeMatteo C, Randall S, Falla K, Lin CY, Giglia L, Mazurek MF, Koelink E. Concussion Management for Children Has Changed: New Pediatric Protocols Using the Latest Evidence. Clin Pediatr (Phila). 2020 Jan;59(1):5-20. doi: 10.1177/0009922819879457. Epub 2019 Oct 18.
Results Reference
background
PubMed Identifier
31396150
Citation
DeMatteo CA, Randall S, Lin CA, Claridge EA. What Comes First: Return to School or Return to Activity for Youth After Concussion? Maybe We Don't Have to Choose. Front Neurol. 2019 Jul 23;10:792. doi: 10.3389/fneur.2019.00792. eCollection 2019.
Results Reference
background
Links:
URL
https://www.canchild.ca/en/research-in-practice/current-studies/the-back2play-app-study
Description
CanChild Research centre website with Back2Play App study updates
URL
https://canchild.ca/en/resources/249-concussion-mild-traumatic-brain-injury-guideline-brochures
Description
CanChild published Return to Activity and Return to School guidelines for Youth recovering from concussion
Learn more about this trial
Development of a Concussion Management Platform for Children and Youth
We'll reach out to this number within 24 hrs