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Fitness to Aid the Brain and Cognitive Skills (Fit ABCS)

Primary Purpose

Pediatric Brain Tumor, Cognitive Impairment

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Web-based Aerobic Exercise Program
Sponsored by
The Hospital for Sick Children
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pediatric Brain Tumor focused on measuring Exercise, Physical functioning

Eligibility Criteria

6 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Between 6 years and 17 years and 11 months of age at time of enrollment
  2. Diagnosed with a brain tumour
  3. 1 to 15 years between diagnosis and time of study enrollment
  4. Medically stable (i.e. must be in remission) as determined by a permanent SickKids staff Neuro-Oncologist
  5. Either declare English as their native language or have at least two years of schooling in English at the time of their first assessment
  6. Have a parent or legal guardian willing to complete the Health and Quality of Life measures
  7. Informed consent (and assent, where applicable) will be obtained from the participants and/or their legal guardians

Exclusion Criteria:

  1. Any condition or diagnosis, that could in the opinion of the Principal Investigator or delegate, interfere with the participant's ability to comply with study instructions, might confound the interpretation of the study results, or put the participant at risk
  2. Diagnosed with a neurodevelopmental or neurological disorder, cerebral palsy, developmental delay or learning disability prior to initial brain tumour diagnosis that would preclude safe participation
  3. Receiving palliative care
  4. Require sedation for neuroimaging
  5. Have ferrous metal implants (i.e. cochlear implant, braces, etc.)
  6. Have a programmable shunt
  7. Pregnant
  8. Completed any prior cognitive rehabilitation intervention within three months of enrollment

Sites / Locations

  • The Hospital for Sick ChildrenRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FitABCS exercise

Arm Description

Web-based community-led, 12-week exercise program

Outcomes

Primary Outcome Measures

Feasibility of the exercise program: The probability that 30 eligible patients will be recruited
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory patient recruitment. The goal is to recruit n=30 participants (≥25% probability) Measure: The Bayesian probability statistic that 30 eligible patients will be recruited
Feasibility of the exercise program: The probability that a recruited participant will attend ≥60% of exercise training sessions
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant attendance. The goal is for a participant to attend ≥60% of exercise training sessions (≥80% probability of participants). Measure: The Bayesian probability statistic that participants will rate the therapeutic alliance between participant/instructor as cooperative and collaborative.
Feasibility of the exercise program: The probability that a recruited participant will complete all study procedures
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant adherence to study procedures (neuroimaging, cognitive, health and quality of life (QOL), cardiovascular fitness and physical functioning assessments). The goal is for a recruited participant to complete all study procedures (≥80% probability). Measure: The Bayesian probability statistic that a recruited participant will complete all study procedures
Feasibility of the exercise program: The probability that instructors will adhere to the web-based platform to deliver exercise training
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory instructor adherence to deliver the program. The goal is for instructors to adhere to the web-based platform to deliver exercise training (≥80% probability). Measure: The Bayesian probability statistic that instructors will adhere to the web-based platform to deliver exercise training
Feasibility of the exercise program: The probability that instructors will develop a therapeutic alliance with the participants
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory rating by the participant of the therapeutic alliance between participants and instructors. The goal is for participants to have a cooperative and collaborative relationship with the instructors, as rated by the Therapeutic Alliance Scales for Children-Revised questionnaire. Measure: The Bayesian probability statistic that the therapeutic alliance between participant/instructor will be comparable across cohorts.
Feasibility of the web-based platform: The probability that instructors will rate the platform as acceptable
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as acceptable (e.g. would recommend to others, would continue to use). The goal is for instructors to rate the the platform as acceptable, indicating ease of use and satisfaction (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as acceptable
Feasibility of the web-based platform: The probability that instructors will rate the platform as relevant
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as relevant (e.g. includes all necessary components to administer an exercise program, would choose to use such a tool to deliver an exercise program).The goal is for the instructors to rate the platform as relevant, indicating the presence of necessary information (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as relevant
Feasibility of the web-based platform: The probability that instructors will rate the platform as efficient
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as efficient (e.g. is useful). The goal is for the instructors to rate the platform as efficient, indicating its usefulness (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as efficient

Secondary Outcome Measures

Full Information

First Posted
April 22, 2022
Last Updated
February 10, 2023
Sponsor
The Hospital for Sick Children
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1. Study Identification

Unique Protocol Identification Number
NCT05367076
Brief Title
Fitness to Aid the Brain and Cognitive Skills
Acronym
Fit ABCS
Official Title
Development of a Web-based Exercise Training Program for Brain Repair and Cognitive Recovery for Paediatric Brain Tumour Survivors in the Community: a Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 7, 2021 (Actual)
Primary Completion Date
October 6, 2023 (Anticipated)
Study Completion Date
October 6, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The Hospital for Sick Children

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
The study will assess the feasibility of a pilot clinical trial of community-led aerobic exercise training for paediatric brain tumour survivors (PBTS) and the feasibility of a web-based platform to deliver this exercise training. It is hypothesized that 12 weeks of community-led exercise training will be feasible for PBTS and the web-based platform will be feasible to deliver exercise training by community-based instructors.
Detailed Description
PBTS will complete 12 consecutive weeks of exercise training. Exercise training will involve 90-minute group sessions of aerobic activity 3 times/week with a 30-minute snack/reward time. The investigators anticipate participants will complete the exercise training program in cohorts, each comprised of a minimum of 3 and maximum of 10 participants. With a minimum of 3 participants per cohort, in order for us to achieve the investigators' goal of recruiting 30 participants, the investigators anticipate running approximately 7 cohorts. Participants will be assigned to a cohort based on proximity to session location and availability to attend sessions. Site Description: This is a single-site trial, as participants will be recruited from SickKids. Community-led exercise training will be delivered at various locations across the Greater Toronto and Hamilton Area (GTHA). Exercise training sessions will be conducted in partnership with Wellspring, a network of community support services across the GTHA for individuals diagnosed and treated for cancer. The investigators have developed a web-based platform for Fitness Trainers/Therapists (FTTs) to i) educate them on working with PBTS, ii) build exercise session plans, and iii) provide feedback on sessions and overall web-based platform functionality and usability. The web-based platform will allow the administration of community-led exercise training in any location. To test the feasibility of the web-based platform, the investigators will be administering exercise training in approximately 5 locations associated with Wellspring centres (and/or surrounding gymnasiums or outdoor space) and Wellspring FTTs. Study Intervention Description: Exercise training will consist of group sessions of aerobic exercise. Each session will include five (5) components: Warm-up activities Aerobic training activities Group sports/games Cool-down activities Snack/reward time The goal of the intervention is to increase and maintain participants' heart rate for at least 30 minutes per session at a minimum of 80% of participants' peak heart rate achieved during a baseline fitness assessment. Increased heart rate will mainly take place during the aerobic circuit training and group sport/game components of each session. Heart rate will be measured using heart rate monitors. Description of study population: Sample size: n = 30 Age: 6-17 years Sex: males and females General health: Patients who have completed treatment for hemispheric or posterior fossa tumours and do not have severe neurological/motor dysfunction that would preclude safe participation in an exercise program Geographic location: Canada

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pediatric Brain Tumor, Cognitive Impairment
Keywords
Exercise, Physical functioning

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
FitABCS exercise
Arm Type
Experimental
Arm Description
Web-based community-led, 12-week exercise program
Intervention Type
Behavioral
Intervention Name(s)
Web-based Aerobic Exercise Program
Intervention Description
Community based FTTs will use a web-based platform to deliver a 12-week exercise training program (120-minute group sessions of aerobic activity 3 times/week). Each session will include: Warm-up activities Aerobic activities and fitness training in a game-like fashion Organized sports/games Cool down activity Snack/reward time
Primary Outcome Measure Information:
Title
Feasibility of the exercise program: The probability that 30 eligible patients will be recruited
Description
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory patient recruitment. The goal is to recruit n=30 participants (≥25% probability) Measure: The Bayesian probability statistic that 30 eligible patients will be recruited
Time Frame
24 Months
Title
Feasibility of the exercise program: The probability that a recruited participant will attend ≥60% of exercise training sessions
Description
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant attendance. The goal is for a participant to attend ≥60% of exercise training sessions (≥80% probability of participants). Measure: The Bayesian probability statistic that participants will rate the therapeutic alliance between participant/instructor as cooperative and collaborative.
Time Frame
24 weeks
Title
Feasibility of the exercise program: The probability that a recruited participant will complete all study procedures
Description
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory participant adherence to study procedures (neuroimaging, cognitive, health and quality of life (QOL), cardiovascular fitness and physical functioning assessments). The goal is for a recruited participant to complete all study procedures (≥80% probability). Measure: The Bayesian probability statistic that a recruited participant will complete all study procedures
Time Frame
24 weeks
Title
Feasibility of the exercise program: The probability that instructors will adhere to the web-based platform to deliver exercise training
Description
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory instructor adherence to deliver the program. The goal is for instructors to adhere to the web-based platform to deliver exercise training (≥80% probability). Measure: The Bayesian probability statistic that instructors will adhere to the web-based platform to deliver exercise training
Time Frame
24 weeks
Title
Feasibility of the exercise program: The probability that instructors will develop a therapeutic alliance with the participants
Description
In order to determine the feasibility of a 12 weeks of community-led exercise training for PBTS, there will be satisfactory rating by the participant of the therapeutic alliance between participants and instructors. The goal is for participants to have a cooperative and collaborative relationship with the instructors, as rated by the Therapeutic Alliance Scales for Children-Revised questionnaire. Measure: The Bayesian probability statistic that the therapeutic alliance between participant/instructor will be comparable across cohorts.
Time Frame
24 weeks
Title
Feasibility of the web-based platform: The probability that instructors will rate the platform as acceptable
Description
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as acceptable (e.g. would recommend to others, would continue to use). The goal is for instructors to rate the the platform as acceptable, indicating ease of use and satisfaction (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as acceptable
Time Frame
24 weeks
Title
Feasibility of the web-based platform: The probability that instructors will rate the platform as relevant
Description
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as relevant (e.g. includes all necessary components to administer an exercise program, would choose to use such a tool to deliver an exercise program).The goal is for the instructors to rate the platform as relevant, indicating the presence of necessary information (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as relevant
Time Frame
24 weeks
Title
Feasibility of the web-based platform: The probability that instructors will rate the platform as efficient
Description
In order to determine the feasibility of a web-based platform to be used by community-based FTTs to deliver exercise training to PBTS, instructors will rate the platform as efficient (e.g. is useful). The goal is for the instructors to rate the platform as efficient, indicating its usefulness (≥80% probability). Measure: The Bayesian probability statistic that instructors will rate the platform as efficient
Time Frame
24 weeks
Other Pre-specified Outcome Measures:
Title
Comparison of community-led vs. historical hospital-led exercise training program: Changes in hippocampal volume
Description
To compare community-led exercise training to historical data from a hospital-led exercise training for PBTS in terms of changes in hippocampal volume using MRI (magnetic resonance imaging). Measures: Anatomical T1 weighted MRI will acquire estimates of hippocampal volume
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led vs. historical hospital-led exercise training program: Changes in neural communication
Description
To compare community-led exercise training to historical data from a hospital-led exercise training for PBTS in terms of changes in neural communication, as estimated by functional connectivity during magnetoencephalography (MEG) recording. Measures: The weighted phase lag index (wPLI) will be used to measure functional connectivity during MEG recording as an estimate of neural communication
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in information processing speed
Description
To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in information processing speed. Measure: Scores on the Rapid Visual Information Processing subtest of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in controlled attention
Description
To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in controlled attention. Measure: Scores on the Match to Sample Visual Search Task subtest of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in declarative memory
Description
To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in declarative memory. Measures: Scores on the Delayed Matching to Sample Task subtest of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in cardiovascular fitness (heart rate, and sub-maximal and maximal work rates)
Description
To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in cardiovascular fitness, including heart rate, sub-maximal and and maximal work rates. Measures: 6-Minute Walk Test and electrically braked cycle ergometer to measure heart rate, and sub-maximal and maximal pro-rated work rates
Time Frame
Baseline, Week 13, and Week 25
Title
Comparison of community-led exercise training to historical data from a hospital-led exercise training program: Changes in physical functioning (bilateral coordination and balance, and running speed/agility and strength)
Description
To compare community-led exercise training to historical data from a hospital-led exercise training program for PBTS in terms of changes in physical functioning, including bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility). Measure: Bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility) using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition. Minimum points scored: 0, maximum points scored: 80; higher scores account for greater motor proficiency (better outcomes)
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in white matter microstructure
Description
To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in white matter microstructure using diffusion kurtosis imaging (DKI) Measures: DKI will acquire kurtosis measures of water diffusion in the brain (mean, axial, radial kurtosis)
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in hippocampal volume
Description
To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes hippocampal volume using Anatomical T1 MRI Measures: Hippocampal volume estimated using Anatomical T1 MRI
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in neural communication
Description
To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in neural communication as estimated by functional connectivity during MEG recording. Measures: The wPLI will be used to measure functional connectivity during MEG recording as an estimate of neural communication
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in information processing speed
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in information processing speed. Measures: Scores on the Pattern Comparison Processing Speed Test subtest of the National Institutes of Health Toolbox and Reaction Time Task subtest RTI subtest of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in controlled attention
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in controlled attention Measures: Scores on the Flanker Inhibitory Control & Attention Task subtest of the National Institutes of Health Toolbox, and the Stop Signal Task, Rapid Visual Information Processing, and Match to Sample Visual Search subtests of the of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in declarative memory
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in declarative memory Measures: Scores on the Children's Auditory Verbal and Learning Test-2 or Rey Auditory Verbal Learning Test (for participants who will be 18 years of age at the time of study completion) and Delayed Matching to Sample subtest of the Cambridge Neuropsychological Test Automated Battery
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in full scale intelligence
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in full scale intelligence. Measures: Scores on the Vocabulary and Matrix Reasoning subtests of the Wechsler Abbreviated Scale of Intelligence-Second Edition
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in MEG behavioural measures
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in MEG behavioural measures. Measures: Reaction time and accuracy scores on the Simple and Choice Visual-Motor Reaction Time Task, and Multi-Source Interference Task during MEG recording
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Health and QOL
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in health and QOL Measure: Scores on the Patient-Reported Outcomes Measurement Information System - Global health 7+2, Pediatric Quality of Life Scale generic core scale, physical activity preference questionnaire and Habitual Physical Activity Scale. All health and QOL measures are parent-proxy reports.
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in cardiovascular fitness (heart rate, and sub-maximal and maximal work rates)
Description
To investigate the impact of community-led exercise training on the following outcomes in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in cardiovascular fitness, including heart rate, sub-maximal and and maximal work rates. Measures: 6-Minute Walk Test and electrically braked cycle ergometer to measure heart rate, and sub-maximal and maximal pro-rated work rates
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in physical functioning (bilateral coordination and balance, and running speed/agility and strength, and ataxia)
Description
To investigate the impact of community-led exercise training in PBTS to provide preliminary data for a subsequent adequately powered randomized controlled trial in terms of changes in physical functioning, including bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility), and ataxia. Measure: Bilateral coordination and balance (body coordination), and running speed/agility and strength (strength and agility) using the Bruininks-Oseretsky Test of Motor Proficiency, Second Edition. Minimum points scored: 0, maximum points scored: 80; higher scores account for greater motor proficiency (better outcomes), strength assessment conducted by a registered Physiotherapist and the Scale for the Assessment and Rating of Ataxia. Minimum points scored: 0, maximum points scored: 40; higher scores indicate increased severity of ataxia (worse outcome)
Time Frame
Baseline, Week 13, and Week 25
Title
Impact of this study intervention on PBTS: Changes in physical functioning as reported by parent (PEDI-CAT)
Description
To investigate the impact of community-let exercise training in PBTS to improve physical functioning in the participant's daily life, as reported by their parent. Measure: Parent report the ease of physical (and cognitive) activities in their child's daily life.
Time Frame
week 25

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Between 6 years and 17 years and 11 months of age at time of enrollment Diagnosed with a brain tumour 1 to 15 years between diagnosis and time of study enrollment Medically stable (i.e. must be in remission) as determined by a permanent SickKids staff Neuro-Oncologist Either declare English as their native language or have at least two years of schooling in English at the time of their first assessment Have a parent or legal guardian willing to complete the Health and Quality of Life measures Informed consent (and assent, where applicable) will be obtained from the participants and/or their legal guardians Exclusion Criteria: Any condition or diagnosis, that could in the opinion of the Principal Investigator or delegate, interfere with the participant's ability to comply with study instructions, might confound the interpretation of the study results, or put the participant at risk Diagnosed with a neurodevelopmental or neurological disorder, cerebral palsy, developmental delay or learning disability prior to initial brain tumour diagnosis that would preclude safe participation Receiving palliative care Require sedation for neuroimaging Have ferrous metal implants (i.e. cochlear implant, braces, etc.) Have a programmable shunt Pregnant Completed any prior cognitive rehabilitation intervention within three months of enrollment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Donald J Mabbott, Ph.D.
Phone
416-813-7654
Ext
308875
Email
donald.mabbott@sickkids.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Cynthia de Medeiros, M.Sc.
Phone
416-813-7396
Ext
307396
Email
cynthia.demederios@sickkids.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Donald J Mabbott
Organizational Affiliation
The Hospital for Sick Children
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Hospital for Sick Children
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 1X8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Donald J Mabbott, Ph.D.
Phone
416-813-7654
Ext
308875
Email
donald.mabbot@sickkids.ca
First Name & Middle Initial & Last Name & Degree
Cynthia de Medeiros, M. Sc.
Phone
416-813-7396
Ext
307396
Email
cynthia.demederios@sickkids.ca

12. IPD Sharing Statement

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Fitness to Aid the Brain and Cognitive Skills

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