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BCAA's in Concussion (HIT HEADS)

Primary Purpose

Brain Concussion

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Branched Chain Amino Acids
Placebo solution
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Concussion focused on measuring Concussion, Branched chain amino acids, BCAA, HIT HEADS

Eligibility Criteria

11 Years - 34 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Males and females, ages 11 - 34 years, of any race.
  2. Subjects who had a concussion, as diagnosed by a qualified physician, within 72 hours prior to enrollment.
  3. Ability to have daily email and internet access.
  4. Females must have a negative urine pregnancy test and must use an acceptable method of contraception.
  5. Subjects must, in the opinion of the referring physician, have the capacity to provide informed consent.
  6. Informed consent by the subject, or for subjects <18 years old both informed consent by a parent/guardian and child assent.

Exclusion Criteria

  1. Witnessed seizure at the time of injury or penetrating head injury.
  2. Prior concussion or TBI within 90 days.
  3. Concussion or TBI severe enough to require admission to an intensive care unit for observation or intervention.
  4. Previous history of TBI or concussion requiring admission to the hospital, disabling stroke, epilepsy, brain tumor, neurodegenerative condition, or psychiatric disease.
  5. Subjects taking neurological or psychoactive medications as a regular daily prescription medication.
  6. Known history of maple syrup urine disease or known family history of maple syrup urine disease.
  7. Any investigational drug use within 30 days prior to enrollment.
  8. Allergy to Food, Drug, and Cosmetic (FD&C) Red #40 (red dye 40) or Sucralose.
  9. Lactating females.
  10. Parents/guardians or subjects who, in the opinion of the investigators, may be non-compliant with study schedules or procedures.

Sites / Locations

  • The Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm Type

Placebo Comparator

Experimental

Experimental

Experimental

Experimental

Arm Label

Placebo

Branched Chain Amino Acids (27g BID)

Branched Chain Amino Acids (22.5g BID)

Branched Chain Amino Acids (15g BID)

Branched Chain Amino Acids (7.5g BID)

Arm Description

Placebo will be administered orally twice daily for 21 days

27 grams of BCAA's will be administered twice-daily for 21 days

22.5 grams of BCAA's will be administered twice-daily for 21 days

15 grams of BCAA's will be administered twice-daily for 21 days

7.5 grams of BCAA's will be administered twice-daily for 21 days

Outcomes

Primary Outcome Measures

Reaction time difference between drug and placebo groups
Processing speed subtest of the Axon Sports Computerized Cognitive Assessment Tool

Secondary Outcome Measures

Clinical symptoms
Evaluate whether BCAA supplementation reduces the time to clinical symptom resolution.
Return to school and sports
Determine whether BCAA supplementation reduces the time to return to school or work, and participation in sports.
Neurocognitive recovery
Determine whether administration of BCAA's reduces the time for neurocognitive recovery for the cognitive domains of attention, learning, and working memory, which are the additional subcomponents of the Axon Sports Computerized Cognitive Assessment Tool.
Compliance and Adherence to Treatment
Adherence to treatment among dosage groups versus placebo and as a function of time.
Tolerability of BCAA's Based on Adverse Events
Assess the tolerability of BCAA doses based on subject reported adverse events.
Safety and BCAA Supplementation
Asses the safety of BCAA doses in concussed athletes through subject reported adverse events (AEs)and serious adverse events (SAEs).

Full Information

First Posted
May 20, 2013
Last Updated
February 2, 2023
Sponsor
Children's Hospital of Philadelphia
Collaborators
The Dana Foundation, Main Line Health, University of Pennsylvania, Pennsylvania Department of Health
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1. Study Identification

Unique Protocol Identification Number
NCT01860404
Brief Title
BCAA's in Concussion
Acronym
HIT HEADS
Official Title
Head Injury Treatment With Healthy and Advanced Dietary Supplements (HIT HEADS): A Randomized, Placebo-controlled, Double-blinded, Therapeutic Exploratory Clinical Trial of Branched Chain Amino Acids (BCAA's) in the Treatment of Concussion
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
January 2014 (Actual)
Primary Completion Date
January 2023 (Actual)
Study Completion Date
January 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
The Dana Foundation, Main Line Health, University of Pennsylvania, Pennsylvania Department of Health

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is a randomized, placebo-controlled, double-blinded, therapeutic exploratory clinical trial of branched chain amino acids (BCAA's) in the treatment of concussion. The aim of the study is to determine whether, compared to placebo treatment, administration of BCAA's, at one or more doses, after a concussion improves neurocognitive recovery at one or more time-periods post concussion.
Detailed Description
Annually, between 100,000 to 140,000 children present to the emergency department for concussion in the United States.1 The Centers for Disease Control now estimates that 1.6 - 3.8 million sports related concussions occur each year in the United States. A large proportion of these patients have enduring cognitive and neurobehavioral problems. Concussion is a heterogeneous insult to the brain that precipitates a complex pathophysiological process that can result in a cascade of deleterious side effects. At present, there are no proven therapies to mitigate or prevent the neurocognitive and neurobehavioral consequences of concussions. The limbic hippocampus, a brain structure crucial for learning and memory, is often damaged in concussion. In preclinical studies in our laboratory, analysis of ipsilateral hippocampi isolated from mice after traumatic brain injury (TBI) demonstrated that only the concentrations of the three BCAA's (valine, isoleucine, and leucine) were significantly altered (reduced) after injury. When these brain-injured animals received dietary supplementation with BCAA's, the concentrations of these amino acids were restored in the injured hippocampus and the injured animals demonstrated significant cognitive improvement to levels comparable to those obtained in non-injured control animals. In light of these results and the increasing awareness and morbidity associated with concussion, we are proposing a pilot therapeutic exploratory clinical trial to determine the effects of BCAA's in reducing the neurocognitive side effects of concussion injury.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Concussion
Keywords
Concussion, Branched chain amino acids, BCAA, HIT HEADS

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo will be administered orally twice daily for 21 days
Arm Title
Branched Chain Amino Acids (27g BID)
Arm Type
Experimental
Arm Description
27 grams of BCAA's will be administered twice-daily for 21 days
Arm Title
Branched Chain Amino Acids (22.5g BID)
Arm Type
Experimental
Arm Description
22.5 grams of BCAA's will be administered twice-daily for 21 days
Arm Title
Branched Chain Amino Acids (15g BID)
Arm Type
Experimental
Arm Description
15 grams of BCAA's will be administered twice-daily for 21 days
Arm Title
Branched Chain Amino Acids (7.5g BID)
Arm Type
Experimental
Arm Description
7.5 grams of BCAA's will be administered twice-daily for 21 days
Intervention Type
Drug
Intervention Name(s)
Branched Chain Amino Acids
Intervention Description
The three BCAA's will be combined together and dissolved in a flavored solution.
Intervention Type
Drug
Intervention Name(s)
Placebo solution
Intervention Description
The placebo solution will have similar taste, texture, consistency and appearance as the BCAA solution.
Primary Outcome Measure Information:
Title
Reaction time difference between drug and placebo groups
Description
Processing speed subtest of the Axon Sports Computerized Cognitive Assessment Tool
Time Frame
Days 3-6, 7-10, 11-14
Secondary Outcome Measure Information:
Title
Clinical symptoms
Description
Evaluate whether BCAA supplementation reduces the time to clinical symptom resolution.
Time Frame
Days 3-6, 7-10, 11-14
Title
Return to school and sports
Description
Determine whether BCAA supplementation reduces the time to return to school or work, and participation in sports.
Time Frame
Days 3-6, 7-10, 11-14
Title
Neurocognitive recovery
Description
Determine whether administration of BCAA's reduces the time for neurocognitive recovery for the cognitive domains of attention, learning, and working memory, which are the additional subcomponents of the Axon Sports Computerized Cognitive Assessment Tool.
Time Frame
Days 3-6, 7-10, 11-14
Title
Compliance and Adherence to Treatment
Description
Adherence to treatment among dosage groups versus placebo and as a function of time.
Time Frame
Day 21
Title
Tolerability of BCAA's Based on Adverse Events
Description
Assess the tolerability of BCAA doses based on subject reported adverse events.
Time Frame
Day 21
Title
Safety and BCAA Supplementation
Description
Asses the safety of BCAA doses in concussed athletes through subject reported adverse events (AEs)and serious adverse events (SAEs).
Time Frame
Day 21

10. Eligibility

Sex
All
Minimum Age & Unit of Time
11 Years
Maximum Age & Unit of Time
34 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Males and females, ages 11 - 34 years, of any race. Subjects who had a concussion, as diagnosed by a qualified physician, within 72 hours prior to enrollment. Ability to have daily email and internet access. Females must have a negative urine pregnancy test and must use an acceptable method of contraception. Subjects must, in the opinion of the referring physician, have the capacity to provide informed consent. Informed consent by the subject, or for subjects <18 years old both informed consent by a parent/guardian and child assent. Exclusion Criteria Witnessed seizure at the time of injury or penetrating head injury. Prior concussion or TBI within 90 days. Concussion or TBI severe enough to require admission to an intensive care unit for observation or intervention. Previous history of TBI or concussion requiring admission to the hospital, disabling stroke, epilepsy, brain tumor, neurodegenerative condition, or psychiatric disease. Subjects taking neurological or psychoactive medications as a regular daily prescription medication. Known history of maple syrup urine disease or known family history of maple syrup urine disease. Any investigational drug use within 30 days prior to enrollment. Allergy to Food, Drug, and Cosmetic (FD&C) Red #40 (red dye 40) or Sucralose. Lactating females. Parents/guardians or subjects who, in the opinion of the investigators, may be non-compliant with study schedules or procedures.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sage Myers, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19995960
Citation
Cole JT, Mitala CM, Kundu S, Verma A, Elkind JA, Nissim I, Cohen AS. Dietary branched chain amino acids ameliorate injury-induced cognitive impairment. Proc Natl Acad Sci U S A. 2010 Jan 5;107(1):366-71. doi: 10.1073/pnas.0910280107. Epub 2009 Dec 7. Erratum In: Proc Natl Acad Sci U S A. 2010 Feb 2;107(5):2373.
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BCAA's in Concussion

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