Trial Study of an Exercise Program for Youth With Persistent Symptoms After Concussion

Comparing Active Rehabilitation to a Comprehensive Education Intervention for Youth With Persistent Post-concussion Symptoms Following Concussion.

The purpose of this randomized control trial study is to determine if an active rehabilitation (low intensity exercise program) in combination with a comprehensive education intervention (standard care) is more effective than the comprehensive education intervention alone in reducing post-concussion symptoms and improving participation in daily activities in youth who have persistent post-concussion symptoms.

Study Overview

Detailed Description

There is a portion of youth who continue to experience persistent post-concussion symptoms beyond the first few weeks of injury. There is limited evidence with respect to the best ways to treat persistent post-concussion symptoms in youth following concussion. There is a small amount of literature that suggests active rehabilitation as a positive intervention for promotion of recovery of persistent post-concussion symptoms. However, this approach to rehabilitation has yet to be explored using a randomized control trial protocol.

Therefore, this study aims to answer the following question: Is a 6 week active rehabilitation program in combination with a comprehensive education intervention (standard care) effective in reducing post-concussive symptoms and improving functional recovery compared to receiving comprehensive education intervention alone among youth experiencing persistent post-concussion symptoms?

We hypothesize:

  1. youth ages 10 to 18 years who present with persistent self-reported post-concussion symptoms 4 weeks after the initial injury and receive the active rehabilitation intervention, will present with decreased post-concussion symptoms at the completion of the intervention.
  2. youth ages 10 to 18 years who receive the active rehabilitation intervention, will present with more complete functional recovery and increased participation in unrestricted physical activity at the completion of the active rehabilitation intervention compared to children receiving the comprehensive education intervention only

Study Type

Interventional

Enrollment (Actual)

1

Phase

  • Not Applicable

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

    • Ontario
      • Toronto, Ontario, Canada, M4G 1R8
        • Holland Bloorview Kids Rehabilitation Hospital

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

10 years to 18 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • confirmed diagnosis of concussion
  • have at least one post-concussion symptom (as measured by the Post Concussion Symptom Inventory)
  • are at least 4 weeks post injury
  • between the ages of 10 and 18 years
  • ability to speak English
  • ability to demonstrate capacity to consent to study

Exclusion Criteria:

  • prior moderate or severe brain injury
  • neck pain/dysfunction or oculormotor/vestibular dysfunction, developmental delays, mental health disorders or chronic pain conditions that prevent participation in active rehabilitation, assessment of gait and balance, or participation in cognitive testing
  • participating in any other physical rehabilitation interventions for post-concussion symptoms (e.g., physiotherapy, massage therapy, chiropractic) at time of enrollment and throughout the duration of the study

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

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Active Rehabilitation
Active Rehabilitation Intervention and Comprehensive Education Intervention (Standard Care)
The active rehabilitation intervention is a 6-week graded rehabilitation program, consisting of four components that are anchored in neuroscience evidence.The four components include: 1) aerobic exercise 2) coordination exercise 3) visualization 4) home program.
An initial education session will be provided by an occupational therapist related to general concussion information and outcomes, as well as strategies for symptom management following concussion.
Active Comparator: Comprehensive Education Intervention
Comprehensive Education Intervention (Standard Care) only
An initial education session will be provided by an occupational therapist related to general concussion information and outcomes, as well as strategies for symptom management following concussion.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Post-Concussion Symptoms
Time Frame: Week 0 (Baseline)
The Post-Concussion Symptom Inventory will be used. This is a self report questionnaire that asks about subjectively experienced symptoms (presence and severity) such as headache, dizziness, memory troubles, after concussion.
Week 0 (Baseline)
Post Concussion Symptoms
Time Frame: Week 2
The Post-Concussion Symptom Inventory will be used. This is a self report questionnaire that asks about subjectively experienced symptoms (presence and severity) such as headache, dizziness, memory troubles, after concussion.
Week 2
Post Concussion Symptoms
Time Frame: Week 6 (upon completion of intervention)
The Post-Concussion Symptom Inventory will be used. This is a self report questionnaire that asks about subjectively experienced symptoms (presence and severity) such as headache, dizziness, memory troubles, after concussion.
Week 6 (upon completion of intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mood
Time Frame: Week 0 (Baseline)
The Beck Depression Inventory for Youth- Second Edition will be used. This is a screen that was designed for youth and provides insight into negative thoughts and feelings towards self, life and future.
Week 0 (Baseline)
Mood
Time Frame: Week 6 (upon completion of the intervention)
The Beck Depression Inventory for Youth- Second Edition will be used. This is a screen that was designed for youth and provides insight into negative thoughts and feelings towards self, life and future.
Week 6 (upon completion of the intervention)
Behavior
Time Frame: Week 0 (Baseline)
The Child Behavior Checklist will be used. It is designed to identify emotional and behavioral concerns in youth.
Week 0 (Baseline)
Behavior
Time Frame: Week 6 (upon completion of the intervention)
The Child Behavior Checklist will be used. It is designed to identify emotional and behavioral concerns in youth.
Week 6 (upon completion of the intervention)
Energy Level
Time Frame: Week 0 (Baseline)
Pediatric Quality of Life Multidimensional Fatigue Scale will be used to examine fatigue
Week 0 (Baseline)
Energy Level
Time Frame: Week 6 (upon completion of the intervention)
Pediatric Quality of Life Multidimensional Fatigue Scale will be used to examine fatigue
Week 6 (upon completion of the intervention)
Quality of Life Level
Time Frame: Week 0 (Baseline)
Pediatric Quality of Life Generic Module will be used to look at quality of life
Week 0 (Baseline)
Quality of Life Level
Time Frame: Week 6 (upon completion of the intervention)
Pediatric Quality of Life Generic Module will be used to look at quality of life
Week 6 (upon completion of the intervention)
SCAT Balance
Time Frame: Week 0 (Baseline)
Sport Concussion Assessment Tool- 3rd Edition Balance Subtest will be used. This measure looks at static balance and postural stability. Youth are asked to perform three different stances on a firm surface for 20 seconds each.
Week 0 (Baseline)
Balance
Time Frame: Week 0 (Baseline)
Bruininks-Oseretsky Test of Motor Proficiency, Second Edition Balance Subtest will be used. This is used to assess static and dynamic balance with focus on the youth's anticipatory postural control.
Week 0 (Baseline)
Balance
Time Frame: Week 6 (upon completion of the intervention)
Bruininks-Oseretsky Test of Motor Proficiency, Second Edition Balance Subtest will be used. This is used to assess static and dynamic balance with focus on the youth's anticipatory postural control.
Week 6 (upon completion of the intervention)
Neurocognitive
Time Frame: Week 0 (Baseline)
ImPACT testing will be done. This is a computer based program designed to assess multiple aspects of cognitive functioning following a concussion.
Week 0 (Baseline)
Neurocognitive
Time Frame: Week 6 (upon completion of the intervention)
ImPACT testing will be done. This is a computer based program designed to assess multiple aspects of cognitive functioning following a concussion.
Week 6 (upon completion of the intervention)
Anxiety
Time Frame: Week 0 (Baseline)
State Trait Anxiety Scale will be used to look at parental anxiety
Week 0 (Baseline)
Anxiety
Time Frame: Week 6 (upon completion of the intervention)
State Trait Anxiety Scale will be used to look at parental anxiety
Week 6 (upon completion of the intervention)
Activity Participation
Time Frame: Week 0 (Baseline)
Physical Activity Questionnaire for Children and Adolescents will be used to look at the physical activities performed in the 7 days prior to evaluation.
Week 0 (Baseline)
Satisfaction Level
Time Frame: Week 0 (Baseline)
Pediatric Quality of Life Health Care Satisfaction Generic Module will be used to gain an understanding of the participants' perceptions of the quality and effectiveness of the intervention.
Week 0 (Baseline)
Acute Concussion Evaluation
Time Frame: Week 0 (Baseline)
Acute Concussion Evaluation will be used to collect demographic information such as characteristics of the injury, signs and symptoms of the injury, and risk factors that may predict prolonged recovery.
Week 0 (Baseline)
Occupational Performance
Time Frame: Week 0 (Baseline)
The Canadian Occupational Performance Measure will be used to identify occupational performance issues as a platform for goal setting. Participants' rate their satisfaction and performance in self-identified activities that they would like to improve their satisfaction and performance in.
Week 0 (Baseline)
Occupational Performance
Time Frame: Week 6 (upon completion of the intervention)
Participants re-rate their satisfaction and performance in the three areas they self-identified as occupational concerns at week 0 (baseline)
Week 6 (upon completion of the intervention)
Balance
Time Frame: Week 6 (upon completion of intervention)
Sport Concussion Assessment Tool- 3rd Edition Balance Subtest will be used. This measure looks at static balance and postural stability. Youth are asked to perform three different stances on a firm surface for 20 seconds each.
Week 6 (upon completion of intervention)
Activity Participation
Time Frame: Week 6 (upon completion of the intervention)
Physical Activity Questionnaire for Children and Adolescents will be used to look at the physical activities performed in the 7 days prior to evaluation.
Week 6 (upon completion of the intervention)
Activity Participation
Time Frame: Week 2
Physical Activity Questionnaire for Children and Adolescents will be used to look at the physical activities performed in the 7 days prior to evaluation.
Week 2
Satisfaction Level
Time Frame: Week 6 (upon completion of the intervention)
Pediatric Quality of Life Health Care Satisfaction Generic Module will be used to gain an understanding of the participants' perceptions of the quality and effectiveness of the intervention.
Week 6 (upon completion of the intervention)

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Nick Reed, PhD, MSc(OT), Holland Bloorview Kids Rehabilitation Hospital/ Bloorview Research Institute

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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

January 1, 2016

Primary Completion (Actual)

December 1, 2017

Study Completion (Actual)

December 1, 2017

Study Registration Dates

First Submitted

October 2, 2014

First Submitted That Met QC Criteria

October 3, 2014

First Posted (Estimate)

October 6, 2014

Study Record Updates

Last Update Posted (Actual)

March 25, 2022

Last Update Submitted That Met QC Criteria

March 10, 2022

Last Verified

March 1, 2022

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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