Biomarkers for Concussion Recovery
Primary Purpose
Concussion, Brain
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
High Volume Aerobic Exercise
Low Volume Aerobic Exercise
Sponsored by
About this trial
This is an interventional treatment trial for Concussion, Brain focused on measuring adolescent, exercise, aerobic, biomarker, recovery
Eligibility Criteria
Inclusion Criteria:
• Adolescent and adult athletes (age 13-18) diagnosed with SRC within 10 days of injury.
Exclusion Criteria:
- Evidence of focal neurological deficit;
- Inability to exercise because of orthopedic or cervical spine injury;
- Increased cardiac risk according to American College of Sports Medicine criteria;
- History of moderate or severe TBI, defined as brain injury with a Glasgow Coma Scale score of 12 or less;
- Current medication treatment for ADHD, learning disorders, depression, anxiety, or other medications that can affect HR;
- Symptom severity score of less than 5 on the initial visit Post Concussion Symptom Scale questionnaire. (7) currently pregnant (8) have any contraindications to exercise (Physical Activity Readiness-Questionnaire)
Sites / Locations
- UB MD Orthopeadics & Sports Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Experimental
Experimental
Active Comparator
Active Comparator
Arm Label
Concussed Participants Group 1
Concussed Participants Group 2
Healthy controls Group 1
Healthy Controls Group 2
Arm Description
High Volume Group
Low Volume Group
High Volume Group
Low Volume Group
Outcomes
Primary Outcome Measures
Persistent Post Concussion Symptoms (PPCS) (Yes/No)
PPCS is defined as more than 28 days from the day of concussive injury (yes) or before 28 days (no). Recovery is defined as asymptomatic, exercise tolerant and confirmation by independent medical examination.
Secondary Outcome Measures
Full Information
NCT ID
NCT05379920
First Posted
March 1, 2022
Last Updated
March 2, 2023
Sponsor
State University of New York at Buffalo
1. Study Identification
Unique Protocol Identification Number
NCT05379920
Brief Title
Biomarkers for Concussion Recovery
Official Title
Epigenetic and Cytokine Biomarkers During Recovery From Sports-Related Concussion
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
March 22, 2022 (Actual)
Primary Completion Date
January 13, 2023 (Actual)
Study Completion Date
January 13, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York at Buffalo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The overarching purpose of this proposed research is to determine whether BDNF and/or specific miRNAs can serve as biomarkers for recovery from a concussion during prescribed exercise. The investigators hypothesize salivary BDNF and specific miRNA signatures will change in a statistically significant manner as participants proceed from injury to recovery and participants who show recovery in ANS regulation will show significant differences in salivary BDNF and specific miRNA expression. This study also aims to determine if BDNF and/or specific miRNA can serve as biomarkers of the return of ANS function in concussed patients. The basic premise here is that the volume of exercise will significantly affect the rate of change in the expression of salivary BDNF and miRNA from injury to recovery.
Detailed Description
This is a four-arm randomized control trial that investigates the changes in expression of BDNF/ miRNA after prescribed exercise intervention in concussed adolescents. Potential participants will be selected from incoming patients to the University Concussion Management Clinic. For a patient to become a potential participant in the "concussed participant" group, a sports medicine physician must first confirm the diagnosis of an acute concussion within 10 days of injury. Healthy controls will be recruited at local high schools (pediatric) and from the UB Clinical Trial registry (pediatric and adult). Concussion diagnosis is based on history, a concussion symptom questionnaire, and a concussion-specific physical examination. If the participant's medical history and demographic information meet eligibility criteria, they will be asked if they would like to participate. All potential participants will be informed of all study procedures verbally. If participants are willing and eligible to participate, they will be asked to consent/ assent to the study procedure.
Participants will be asked to fill out the documentation regarding their demographics, concussion symptoms/history (Concussion Symptom Evaluation, Post-Concussion Symptom Inventory), and motivation to exercise (Modified Perceived Competence Scale, Modified Treatment Self-Regulation Questionnaire). Additionally, to determine if participants have any contraindications to exercise, the Physical Activity Readiness Questionnaire (PAR-Q) will be completed by all participants.
Participants will undergo the Buffalo Concussion Physical Exam (BCPE), a short examination to used determine if a patient is concussed. This examination includes vital signs, a head and neck examination, cranial nerve testing, oculomotor testing, and a balance test.
A trained examiner will complete an Oral Hygiene Index-Simplified (OHI-S) and will collect saliva. The Oral Hygiene Index is a short evaluation of the calculus and debris on selected teeth to assess the oral hygiene of a participant. Saliva will be collected using a Genotek Swab (miRNA) and a Salimetrics Cryovial (BDNF). Saliva will be collected with a swab (Genotek) and passive drool (Salimetrics) techniques.
After saliva is obtained, the participant will be asked to complete the Buffalo Concussion Treadmill Test (BCTT). The BCTT is a graded exercise test that is used to determine concussion-related exercise intolerance. Although it is standard for patients from the Concussion Clinic to require a BCTT assessment as a part of their standard visit, participants will be made aware that their BCTT data will be used for this study. During the BCTT participants will be asked to wear an HR monitor (Polar H10) for the collection of HR and Heart Rate Variability (HRV) data.
After completion of the BCTT, the examiner will use the results of the exercise test to create an individualized exercise prescription. The prescription will be randomized for high and low volumes and even split between male and female participants in healthy and concussed groups.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Concussion, Brain
Keywords
adolescent, exercise, aerobic, biomarker, recovery
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly assigned into 4-arms: (1) Concussed participants: high volume exercise, (2) Concussed participants: low volume exercise, (3) Healthy controls: high volume exercise, (4) Healthy controls: low volume exercise. Each group will consist of 50% males and 50% females. Exercise interventions for all participants are adjusted to the 90% Heart rate threshold (HRt) collected on the BCTT. The high-volume group will exercise aerobically at 90% of their HRt for 5 days a week for 30 minutes. The low volume group will exercise aerobically at 90% of their HRt for 3 days a week for 30 minutes. The intervention will last 2 weeks. Participants will return to the clinic and repeat testing on Days 7 and 14. Recovery is defined as (1) resolution of concussion symptoms (2) physical examination within normal limits; (3) ability to exercise to at least 80% of age-appropriate maximum HR without exacerbation of concussion-like symptoms on the BCTT.
Masking
Care Provider
Allocation
Randomized
Enrollment
60 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Concussed Participants Group 1
Arm Type
Experimental
Arm Description
High Volume Group
Arm Title
Concussed Participants Group 2
Arm Type
Experimental
Arm Description
Low Volume Group
Arm Title
Healthy controls Group 1
Arm Type
Active Comparator
Arm Description
High Volume Group
Arm Title
Healthy Controls Group 2
Arm Type
Active Comparator
Arm Description
Low Volume Group
Intervention Type
Behavioral
Intervention Name(s)
High Volume Aerobic Exercise
Intervention Description
Aerobic exercise is completed for 30 minutes, 5 days a week. Exercise intensity is adjusted weekly to 90% of the heart rate threshold. Exercise interventions for all participants are adjusted to the 90% Heart rate threshold (HRt) collected on the BCTT.
Intervention Type
Behavioral
Intervention Name(s)
Low Volume Aerobic Exercise
Intervention Description
Aerobic exercise is completed for 20 minutes, 3 days a week. Exercise intensity is adjusted weekly to 90% of the heart rate threshold. Exercise interventions for all participants are adjusted to the 90% Heart rate threshold (HRt) collected on the BCTT.
Primary Outcome Measure Information:
Title
Persistent Post Concussion Symptoms (PPCS) (Yes/No)
Description
PPCS is defined as more than 28 days from the day of concussive injury (yes) or before 28 days (no). Recovery is defined as asymptomatic, exercise tolerant and confirmation by independent medical examination.
Time Frame
28 days
10. Eligibility
Sex
All
Gender Based
Yes
Gender Eligibility Description
Self-representation of gender identity
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
• Adolescent and adult athletes (age 13-18) diagnosed with SRC within 10 days of injury.
Exclusion Criteria:
Evidence of focal neurological deficit;
Inability to exercise because of orthopedic or cervical spine injury;
Increased cardiac risk according to American College of Sports Medicine criteria;
History of moderate or severe TBI, defined as brain injury with a Glasgow Coma Scale score of 12 or less;
Current medication treatment for ADHD, learning disorders, depression, anxiety, or other medications that can affect HR;
Symptom severity score of less than 5 on the initial visit Post Concussion Symptom Scale questionnaire. (7) currently pregnant (8) have any contraindications to exercise (Physical Activity Readiness-Questionnaire)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Leddy, MD
Organizational Affiliation
University at Buffalo
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Barry Willer, PhD
Organizational Affiliation
University at Buffalo
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Praveen Arany, DDS, PhD
Organizational Affiliation
University at Buffalo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mohammad Nadir, MD, PhD
Organizational Affiliation
University at Buffalo
Official's Role
Study Director
Facility Information:
Facility Name
UB MD Orthopeadics & Sports Medicine
City
Buffalo
State/Province
New York
ZIP/Postal Code
14214
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
No plan to share IPD currently
Learn more about this trial
Biomarkers for Concussion Recovery
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