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Early Sub-threshold Exercise Treatment for Concussion

Primary Purpose

Concussion, Mild

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Aerobic Exercise
Rest
Stretching
Sponsored by
State University of New York at Buffalo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Concussion, Mild

Eligibility Criteria

13 Years - 18 Years (Child, Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • 13-18 years; any race, ethnicity, or sex.
  • Concussion sustained 2-7 days prior to first clinical visit.
  • Symptom score (new symptoms) >3 on the Post-Concussion Symptom Inventory Scale.
  • Glasgow Coma Scale (GCS) of 13-15 (if available in medical record), an alteration in mental status, loss of consciousness (if present) of less than 30 minutes, and post-traumatic amnesia (if present) limited to <24 hours.
  • Low risk for cardiac disease and willing to exercise.
  • Medications, except for βeta- and calcium-blockers, are acceptable.

Exclusion Criteria:

  • GCS score <13 at time of injury.
  • Lesion on CT/MRI (via review of emergency department records) and/or focal neurologic deficit consistent with an intracerebral lesion (e.g., unilateral weakness, dilated pupil).
  • Inability to exercise because of orthopedic injury, significant vestibular dysfunction, visual abnormality, or increased cardiac risk.
  • Neurosurgical intervention, general anesthesia and previously diagnosed neurological or psychiatric diseases.
  • Additional head injury after study enrollment.
  • Active substance abuse/dependence.
  • Non-fluency in English.
  • βeta- and calcium blocker use.
  • Autism, metal braces or other metal that would interfere with ASL.
  • Unwilling to exercise.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Active Comparator

    Placebo Comparator

    Placebo Comparator

    Arm Label

    Aerobic Exercise

    Stretching

    Rest

    Arm Description

    Sub-threshold aerobic exercise.

    Stretching program that will not raise heart rate.

    Relative rest. Avoid all structured exercise.

    Outcomes

    Primary Outcome Measures

    Time to recovery
    Time to baseline level of symptoms on Post Concussion Symptom Inventory (PCSI) for 2 days in a row

    Secondary Outcome Measures

    Autonomic function
    Autonomic function as assessed by the Cold Pressor Test (CPT)
    Delayed recovery
    Persistence of increased symptoms on the PCSI at 1 and at 4 months after concussion
    Cerebral Blood Flow (CBF)
    CBF by Arterial Spin Labelling MRI

    Full Information

    First Posted
    June 5, 2018
    Last Updated
    October 16, 2020
    Sponsor
    State University of New York at Buffalo
    Collaborators
    Children's Hospital of Philadelphia, Harvard University, The Mind Research Network
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03569709
    Brief Title
    Early Sub-threshold Exercise Treatment for Concussion
    Official Title
    Guided Aerobic Exercise Therapy to Improve Recovery From Acute Concussion: A Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2020
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Not funded
    Study Start Date
    June 15, 2018 (Anticipated)
    Primary Completion Date
    December 15, 2020 (Anticipated)
    Study Completion Date
    December 15, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    State University of New York at Buffalo
    Collaborators
    Children's Hospital of Philadelphia, Harvard University, The Mind Research Network

    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
    Each year millions of Americans suffer concussions as a result of accidents in sports, at work or through military service. Adolescents take the longest to recover from the effects of concussion yet no therapy exists to help speed their recovery. This project aims to see if a program of early guided aerobic exercise can safely speed recovery from concussion in adolescents and investigates some reasons for why this type of therapy could be effective.
    Detailed Description
    Most children with concussion recover spontaneously within 2-4 weeks of injury but approximately 30% experience prolonged post-concussive symptoms (PPCS), impacting quality of life. There are no evidence-based therapies for acute pediatric concussion. Instead, current consensus-based-recommendations include physical and cognitive rest as the mainstays of treatment despite evidence to the contrary that excessive rest prolongs recovery and that early (first week) activity reduces PPCS incidence. The investigators were the first to demonstrate that a systematic evaluation of exercise tolerance using the Buffalo Concussion Treadmill Test (BCTT) to prescribe a guided exercise prescription in those with PPCS safely sped recovery. The investigators have preliminary data that exercise may speed recovery if administered within the first week after sport-related concussion (SRC). Concussion is associated with adverse effects on the autonomic nervous system (ANS) and control of cerebral blood flow (CBF). The investigators have shown that sub-threshold aerobic exercise reduces symptoms in PPCS in association with normalization of ANS function and CBF control, providing a potential mechanism of action as well as target engagement for this non-pharmacological therapy. An important translational aspect is that the BCTT would be for clinicians a clinical proxy of concussion physiology that would help make the difficult return-to-activity/play decision more objective and physiologically-based. The investigators' long-term goals are to develop therapies that safely speed recovery from concussion, return youth back to their typical activities, actively prevent PPCS, and develop practical physiological tools for clinicians. The overall objective of this application is to determine if early guided aerobic exercise speeds recovery from SRC. The investigators specifically test underlying mechanisms of action for faster recovery by measuring ANS function (the cold pressor test, CPT) and CBF (by Arterial Spin Labeling, ASL). Age- and sex-matched healthy controls will be recruited to quantify physiological CBF differences and serve as a normative control group. The investigators will examine these questions in a randomized, multisite controlled trial in adolescents aged 13-18y with acute SRC by pursuing the following two specific aims: (1) determine if guided aerobic exercise/education speeds recovery after acute concussion in adolescents compared with (a) rest/education with a gradual return to activities, (i.e., current recommendation) and (b) a progressive stretching program/education (attention placebo); and (2) as secondary aims the investigators will quantify the effects of each intervention in Aim 1 on CBF and on autonomic function (CPT), which serve as relevant and objective physiological measures of autonomic regulation of CBF following concussion. This project will provide critical evidence to support the role of guided aerobic exercise for the active treatment of acute concussion and for a physiological mechanism(s) for its effect, which would lead to a paradigm shift from the current passive approach to treatment. The translational aspect of the project is unique and would have immediate impact to help clinicians determine recovery based on physiology rather than symptoms. A controlled active approach to concussion treatment may also substantially reduce the incidence of PPCS in children.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Concussion, Mild

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomized Controlled Trial
    Masking
    Care ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Aerobic Exercise
    Arm Type
    Active Comparator
    Arm Description
    Sub-threshold aerobic exercise.
    Arm Title
    Stretching
    Arm Type
    Placebo Comparator
    Arm Description
    Stretching program that will not raise heart rate.
    Arm Title
    Rest
    Arm Type
    Placebo Comparator
    Arm Description
    Relative rest. Avoid all structured exercise.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Aerobic Exercise
    Intervention Description
    Progressive sub-threshold aerobic exercise
    Intervention Type
    Behavioral
    Intervention Name(s)
    Rest
    Intervention Description
    No structured exercise.
    Intervention Type
    Behavioral
    Intervention Name(s)
    Stretching
    Intervention Description
    Gentle progressive upper and lower extremity stretching program
    Primary Outcome Measure Information:
    Title
    Time to recovery
    Description
    Time to baseline level of symptoms on Post Concussion Symptom Inventory (PCSI) for 2 days in a row
    Time Frame
    up to 2 days
    Secondary Outcome Measure Information:
    Title
    Autonomic function
    Description
    Autonomic function as assessed by the Cold Pressor Test (CPT)
    Time Frame
    Within one week of injury and at 1 month after injury
    Title
    Delayed recovery
    Description
    Persistence of increased symptoms on the PCSI at 1 and at 4 months after concussion
    Time Frame
    1 and 4 months after concussion
    Title
    Cerebral Blood Flow (CBF)
    Description
    CBF by Arterial Spin Labelling MRI
    Time Frame
    Within one week of injury and at 1 month after injury

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    13 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: 13-18 years; any race, ethnicity, or sex. Concussion sustained 2-7 days prior to first clinical visit. Symptom score (new symptoms) >3 on the Post-Concussion Symptom Inventory Scale. Glasgow Coma Scale (GCS) of 13-15 (if available in medical record), an alteration in mental status, loss of consciousness (if present) of less than 30 minutes, and post-traumatic amnesia (if present) limited to <24 hours. Low risk for cardiac disease and willing to exercise. Medications, except for βeta- and calcium-blockers, are acceptable. Exclusion Criteria: GCS score <13 at time of injury. Lesion on CT/MRI (via review of emergency department records) and/or focal neurologic deficit consistent with an intracerebral lesion (e.g., unilateral weakness, dilated pupil). Inability to exercise because of orthopedic injury, significant vestibular dysfunction, visual abnormality, or increased cardiac risk. Neurosurgical intervention, general anesthesia and previously diagnosed neurological or psychiatric diseases. Additional head injury after study enrollment. Active substance abuse/dependence. Non-fluency in English. βeta- and calcium blocker use. Autism, metal braces or other metal that would interfere with ASL. Unwilling to exercise.

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

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