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NCT03674398 · ClinicalTrials.gov registry record · NA

Aerobic Exercise and Cognitive Training Effects on Postconcussive Symptomology

A NA study of Post-Concussion Syndrome and Acquired Brain Injury, sponsored by University of Illinois at Urbana-Champaign.

Completed
Registry status
NA
Development phase
34
Enrollment target
1
Study location

NCT03674398 is a NA study of Post-Concussion Syndrome and Acquired Brain Injury that has completed, run by University of Illinois at Urbana-Champaign. The registered enrollment target is 34 participants, below the 58-participant average among 14 other Post-Concussion Syndrome trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03674398, a NA study of Post-Concussion Syndrome and Acquired Brain Injury, has completed, sponsored by University of Illinois at Urbana-Champaign.

COMPLETED
Registry status
NA
Development phase
34 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to compare a 4-week, moderately intensive, lab and home-based aerobic exercise program versus exercise plus cognitive training. Participants will include individuals who experience lingering symptoms of a head injury or concussion.

Conditions Studied

Post-Concussion Syndrome Acquired Brain Injury Head Injury Post-Traumatic Headache mTBI - Mild Traumatic Brain Injury Post-Concussive Syndrome, Chronic Closed Head Injury

Interventions

  • BEHAVIORAL Exercise+CT
  • BEHAVIORAL Exercise only

Study Locations (1)

Illinois

  • University of Illinois at Urbana-Champaign - Urbana

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2018-10-01
Est. Completion 2019-05-03
Phase NA

Sponsor

University of Illinois at Urbana-Champaign

129 total trials

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What the Registry Record Tells You About NCT03674398

The ClinicalTrials.gov registry entry for NCT03674398 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 58-participant average among 14 other Post-Concussion Syndrome trials with a reported enrollment target (41% lower). The listed sponsor is University of Illinois at Urbana-Champaign, which has 129 total studies on file at ClinicalTrials.gov.

The record links to 7 conditions, with Post-Concussion Syndrome appearing as the primary indexed condition, and to 2 interventions - of which Exercise+CT is the first listed.

NCT03674398 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.

Frequently Asked Questions

What is clinical trial NCT03674398 about?

NCT03674398 is a clinical study titled "Aerobic Exercise and Cognitive Training Effects on Postconcussive Symptomology". The purpose of this study is to compare a 4-week, moderately intensive, lab and home-based aerobic exercise program versus exercise plus cognitive training. Participants will include individuals who experience lingering symptoms of a head injury or concussion.

What is the current status of trial NCT03674398?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2018-10-01. Estimated completion is 2019-05-03.

What conditions does trial NCT03674398 study?

This clinical trial studies the following conditions: Post-Concussion Syndrome, Acquired Brain Injury, Head Injury, Post-Traumatic Headache, mTBI - Mild Traumatic Brain Injury.

What interventions are being tested in trial NCT03674398?

The interventions under investigation include: Exercise+CT (BEHAVIORAL), Exercise only (BEHAVIORAL).

Who is sponsoring clinical trial NCT03674398?

This trial is sponsored by University of Illinois at Urbana-Champaign, which has 129 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03674398 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.