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Acute Concussion Therapy Intervention Training in Healthy and Concussed Participants (ACTIVE)

Primary Purpose

Cerebral Concussion

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ACTIVE Training
Sponsored by
University of North Carolina, Chapel Hill
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebral Concussion focused on measuring Concussion, Exercise

Eligibility Criteria

18 Years - 30 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Diagnosed as having a concussion by a physician within three days of study enrollment (concussed participants only)
  • Glasgow Coma Scale >13 (concussed participants only)
  • Participants must be active, which is defined as 30 or more minutes of moderate to vigorous physical activity 3 or more days per week. All healthy participants must met this definition and concussed participants should have met this definition prior to injury.
  • Good cardiovascular health (subject to approval from study physician)

Exclusion Criteria:

  • Recreational drug use over the course of study participation
  • Associated injuries (broken bones, etc.) that would limit the ability to successfully complete ACTIVE training
  • For healthy participants, no history of concussion within the last year
  • For concussed participants, skull fracture or brain bleed at time of the injury
  • UNC Varsity athletes

Sites / Locations

  • University of North Carolina at Chapel Hill

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

ACTIVE Training

Control

Arm Description

Healthy participants will be progressed from 60-80% of their VO2max as determined by the progressive exercise test over the course of 6 30-minute training sessions. Concussed participants will begin 30-minute training sessions at 60% of the VO2 achieved at symptom exacerbation of the exercise test. Intensity will be progressed as tolerated by the participant and training sessions will continue until the participant is asymptomatic for 24 consecutive hours (total number of sessions variable based on clinical recovery).

Healthy controls will be asked to follow their normal routine for rest and physical activity. Concussed controls will be asked to follow the guidance for rest and activity as prescribed by the physicians and athletic trainers overseeing their clinical care.

Outcomes

Primary Outcome Measures

Average Days to Recovery
Average number of days from injury to recovery (recovery is defined as full clearance by physician)

Secondary Outcome Measures

Average Change in Mental Status
SAC Total Score (Out of 30 possible points; combination of scores from orientation (5), immediate memory (15), concentration (5), and delayed memory (5) sections; higher scores are indicative of better results)
Average Changed in Balance
BESS Total Score (Participants are given errors for positions of poor postural control; out of 60 points; higher scores are indicative of poorer performance)
Average Change in Cognition
CNS Composite Score (percentile of participant's overall achievement on a computerized neurocognitive test; higher percentiles indicate better performance)
Average Change in Near-Point Convergence
Near-point convergence distance (average distance- over three trials- of convergence during vision, higher scores indicate poorer convergence)
Average Change in Concussive Symptoms
GSC Total Score (incorporates presence and severity for a total score on 27-items, each item rated from 0 (not present) to 6 (severe); higher scores indicate worse symptoms

Full Information

First Posted
July 27, 2016
Last Updated
February 15, 2017
Sponsor
University of North Carolina, Chapel Hill
Collaborators
American College of Sports Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT02872480
Brief Title
Acute Concussion Therapy Intervention Training in Healthy and Concussed Participants
Acronym
ACTIVE
Official Title
The Effect of ACTIVE Training in Improving Clinical Outcomes in Healthy and Acutely Concussed College-aged Participants
Study Type
Interventional

2. Study Status

Record Verification Date
February 2017
Overall Recruitment Status
Completed
Study Start Date
August 2016 (undefined)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
February 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of North Carolina, Chapel Hill
Collaborators
American College of Sports Medicine

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Healthy (non-injured) and concussed college-aged participants will complete two testing sessions that include (1) clinical symptom, balance, and cognitive evaluations and (2) a progressive exercise session to establish symptom exacerbation or maximal exercise capacity. Individuals randomized to the control group will receive no intervention between sessions, while individuals randomized to the intervention group will complete 30 minutes of stationary bike exercise at least 3 days/week.
Detailed Description
Healthy and concussed participants will be randomized to ACTIVE training (intervention) or control (no intervention) groups. Participants, regardless of group assignment, will receive clinical symptom, balance, and cognitive evaluations as well as a progressive exercise assessment at study outset. Concussed participants will enroll into the study within three days of injury and study participation will termination following 24 consecutive hours with no reported concussive symptoms. Healthy participants will have arbitrary start dates and will terminate the study 10-14 days later to approximate the general length of concussion recovery and, therefore, make the time between session in the healthy and concussed cohorts as equivalent as possible. Participants in the intervention group will complete stationary cycle ergometer workouts for 30 mins at least 3 days per week between testing sessions. Healthy participants will complete six ACTIVE training sessions, while concussed participants will complete ACTIVE training at least three days per week until asymptomatic. Concussed control participants will follow physician guidelines for rest and activity, while healthy control participants will be asked to follow their typical routines for rest and activity. Participants will repeat the identical testing session assessments prior to study termination.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebral Concussion
Keywords
Concussion, Exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ACTIVE Training
Arm Type
Experimental
Arm Description
Healthy participants will be progressed from 60-80% of their VO2max as determined by the progressive exercise test over the course of 6 30-minute training sessions. Concussed participants will begin 30-minute training sessions at 60% of the VO2 achieved at symptom exacerbation of the exercise test. Intensity will be progressed as tolerated by the participant and training sessions will continue until the participant is asymptomatic for 24 consecutive hours (total number of sessions variable based on clinical recovery).
Arm Title
Control
Arm Type
No Intervention
Arm Description
Healthy controls will be asked to follow their normal routine for rest and physical activity. Concussed controls will be asked to follow the guidance for rest and activity as prescribed by the physicians and athletic trainers overseeing their clinical care.
Intervention Type
Other
Intervention Name(s)
ACTIVE Training
Intervention Description
Participants will be asked to complete aerobic exercise on a stationary bike during 30-minute sessions. Intensity will progress under a standard procedure for healthy participants (60-80% of VO2max) and as tolerated by concussed participants (starting at 60% of symptom exacerbation).
Primary Outcome Measure Information:
Title
Average Days to Recovery
Description
Average number of days from injury to recovery (recovery is defined as full clearance by physician)
Time Frame
Assessed every 24 hours from baseline to study termination for each participant (approximately 10-14 days)
Secondary Outcome Measure Information:
Title
Average Change in Mental Status
Description
SAC Total Score (Out of 30 possible points; combination of scores from orientation (5), immediate memory (15), concentration (5), and delayed memory (5) sections; higher scores are indicative of better results)
Time Frame
Each participant will complete the SAC at baseline (first testing session) and recovery (full clearance by physician)- approximately 10-14 days apart
Title
Average Changed in Balance
Description
BESS Total Score (Participants are given errors for positions of poor postural control; out of 60 points; higher scores are indicative of poorer performance)
Time Frame
Each participant will complete the BESS at at baseline (first testing session) and recovery (full clearance by physician)- approximately 10-14 days apart
Title
Average Change in Cognition
Description
CNS Composite Score (percentile of participant's overall achievement on a computerized neurocognitive test; higher percentiles indicate better performance)
Time Frame
Each participant will complete CNS at at baseline (first testing session) and recovery (full clearance by physician)- approximately 10-14 days apart
Title
Average Change in Near-Point Convergence
Description
Near-point convergence distance (average distance- over three trials- of convergence during vision, higher scores indicate poorer convergence)
Time Frame
Each participant will complete the VOMS at at baseline (first testing session) and recovery (full clearance by physician)- approximately 10-14 days apart
Title
Average Change in Concussive Symptoms
Description
GSC Total Score (incorporates presence and severity for a total score on 27-items, each item rated from 0 (not present) to 6 (severe); higher scores indicate worse symptoms
Time Frame
Healthy participants will complete the GSC at at baseline (first testing session) and recovery (full clearance by physician)- approximately 10-14 days apart

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosed as having a concussion by a physician within three days of study enrollment (concussed participants only) Glasgow Coma Scale >13 (concussed participants only) Participants must be active, which is defined as 30 or more minutes of moderate to vigorous physical activity 3 or more days per week. All healthy participants must met this definition and concussed participants should have met this definition prior to injury. Good cardiovascular health (subject to approval from study physician) Exclusion Criteria: Recreational drug use over the course of study participation Associated injuries (broken bones, etc.) that would limit the ability to successfully complete ACTIVE training For healthy participants, no history of concussion within the last year For concussed participants, skull fracture or brain bleed at time of the injury UNC Varsity athletes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth F Teel, M.S.
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jason P Mihalik, Ph.D.
Organizational Affiliation
University of North Carolina, Chapel Hill
Official's Role
Study Chair
Facility Information:
Facility Name
University of North Carolina at Chapel Hill
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
27599
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30562056
Citation
Teel EF, Register-Mihalik JK, Appelbaum LG, Battaglini CL, Carneiro KA, Guskiewicz KM, Marshall SW, Mihalik JP. Randomized Controlled Trial Evaluating Aerobic Training and Common Sport-Related Concussion Outcomes in Healthy Participants. J Athl Train. 2018 Dec;53(12):1156-1165. doi: 10.4085/1062-6050-7-18. Epub 2018 Dec 18.
Results Reference
derived

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Acute Concussion Therapy Intervention Training in Healthy and Concussed Participants

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