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Sports Related ConcussionSRCNCT07175753

Chiropractic Neuroscience Care in Sports Concussion

An observational study of Sports Related Concussion, run by Life University at 1 site in United States.

Enrolling by invitation

Enrolling by invitation. The study team selects and invites participants, usually from an existing group of patients.

Sites and contacts
Official record
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Trial summary

The goal of this study is to evaluate our study design and the potential effect of chiropractic-applied clinical neuroscience care on individuals with sports-related concussion (SRC) in individuals between the ages 18 and 40.The main question it aims to answer is: Is there any potential effect of chiropractic… Read more about this study

Who is it for?
Ages 18 to 40 years
Conditions the study is for
Sports Related Concussion
What is being tested?
chiropractic applied clinical neuroscience care
How many people
20 participants
Where
1 siteUnited States
Study dates
7 Nov 2025to 16 Jul 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 40 years
  • All sexes
  • No healthy volunteers
  • Adult

Study population: Individuals between the ages 18 and 40 experiencing sports related concussion and symptoms such as headache, nausea, dizziness, loss of consciousness, amnesia, balance impairment, irritability, visual disturbance, slowed reaction times, etc.

Who may be able to join

  • Currently active athletes affiliated with the Life University Athletics Department
  • Aged between 18 and 40 years
  • Experiencing sport-related concussion symptoms, including but not limited to:
  • Headache
  • Nausea
  • Dizziness
Show all 12Show fewer
  • Loss of consciousness
  • Amnesia
  • Balance impairment
  • Irritability
  • Visual disturbance
  • Slowed reaction times

Who cannot join

  • Not affiliated with the Life University Athletics Department
  • Younger than 18 or older than 40 years
  • No current symptoms of sport-related concussion

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

United States1 site
  • NeuroLife Institute

    Marietta, Georgia, 30060

Other trials in United States

About this study

Official title: The Effects of Chiropractic Applied Clinical Neuroscience Care on Sports-Related Concussion Patients: An Observational Study

The goal of this study is to evaluate our study design and the potential effect of chiropractic-applied clinical neuroscience care on individuals with sports-related concussion (SRC) in individuals between the ages 18 and 40.The main question it aims to answer is:

  • Is there any potential effect of chiropractic neuroscience care on sports related concussion patients?

Participants will be assessed on their attention, processing speed, fine motor function, standing balance, auditory function, and emotional state as part of the study using the NIH toolbox.

Read the detailed description

The investigators shall recruit 20 participants for this study who are currently active athletes affiliated with the Life University Athletics Department, aged between 18 and 40 years and have sport-related concussion symptoms such as headache, nausea, dizziness, loss of consciousness, amnesia, balance impairment, irritability, visual disturbance, slowed reaction times, etc.

Subjects will do the following tasks:

  1. Attention and Self-Control Test: In this test participants will look at rows of five fish on a screen and choose the direction of the middle fish while ignoring the others and press a button to show the direction of the middle fish.
  2. Processing Speed Test: Participants will see two pictures side by side and decide if the pictures are the same or different and press a button as fast as they can.
  3. Hand Skill Test: Subjects will be asked to do a hand skill/coordination test (called the 9-Hole Pegboard Test), where they place small pegs into holes and take them out as quickly as they can.
  4. Standing Balance Test: In this test participants will stand still in various positions, sometimes with your eyes open and sometimes closed, on both hard ground and a soft foam pad, while trying to remain as still as possible. On one part of the test, they will stand with one foot in front of the other.
  5. Hearing in Noise Test: Subjects will listen to words through headphones while background noise is playing. They will repeat the words they hear.
  6. Emotion Surveys: They will answer questions about their feelings and relationships. These include how often they feel angry, sad, or lonely, and how happy or satisfied they feel with their life.

Assessments will be approximately 80 minutes over two sessions.

Being tested
chiropractic applied clinical neuroscience care
Keywords
Sports related concussion, Chiropractic clinical care

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • chiropractic applied clinical neuroscience careOther

    Standard chiropractic care with physiotherapy and phototherapy over two sessions

Study groups in NCT07175753
Study groupRoleWhat they receive
SRC GroupThose who have sport-related concussion symptoms such as headache, nausea, dizziness, loss of consciousness, amnesia, balance impairment, irritability, visual disturbance, slow reaction times, etc.
Receives: Other: chiropractic applied clinical neuroscience care

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of Participants Who Complete All Study Visits and Procedures

    The number of participants who complete all scheduled study visits, tests, and treatments without early withdrawal. This measure assesses participant tolerability and compliance with the full study protocol. The unit of measure is the number of participants completing full study protocol.

    Measured: 1 year

  2. Recruitment

    Number of participant enrolled in the study within the recruitment period.

    Measured: 1 year

  3. Retention

    Number of participants who remain enrolled and complete the study protocol.

    Measured: 1 year

  4. Adherence

    Number of completed required study visits and treatments per participant.

    Measured: 1 year

Secondary outcomes (10)
  1. Change in Executive Function, Attention, and Inhibitory Control

    Change from baseline in Flanker Inhibitory Control and Attention Test (FICAT) scores using the NIH Toolbox. The unit of measure is the T score on FICAT.

    Measured: 1 year

  2. Change in Visual Processing Speed

    Change from baseline in Pattern Comparison Processing Speed Test (PCPS) scores using the NIH Toolbox. The unit of measure is T score of the PCPS.

    Measured: 1 year

  3. Change in Fine Motor Skills and Dexterity

    Change from baseline in 9-Hole Pegboard Dexterity Test scores using the NIH Toolbox. Unit of measure is time in seconds to complete task (9-Hole Pegboard Test, NIH Toolbox)

    Measured: 1 year

  4. Change in Postural Stability and Balance

    Change from baseline in Balance Test scores using the NIH Toolbox Balance V3, Unit of measure is time in seconds using the NIH Toolbox Balance V3.

    Measured: 1 year

  5. Change in Auditory Processing and Speech Recognition in Noise

    Change from baseline in Words-In-Noise (WIN) Test scores using the NIH Toolbox. Unit of measure is T score from WIN Test.

    Measured: 1 year

  6. Change in Negative Affect of Anger and Sadness

    Change from baseline in Emotional Battery Test scores using the NIH toolbox. Unit of measure is T score of Emotional Battery Test using NIH toolbox.

    Measured: 1

  7. Change in Emotional Support and Loneliness

    Change from baseline in social relationships using Emotional Battery Test scores using the NIH toolbox. Unit of measure is T score of Emotional Battery Test.

    Measured: 1

  8. Change in Psychological Well-being (General Life Satisfaction and Positive Affect)

    Change from baseline in psychological well-being using the Emotional Battery Test scores using the NIH toolbox. Unit of measure is T score of Emotional Battery Test using NIH toolbox.

    Measured: 1 year

  9. Acceptability from Participant Perspective

    Participant ratings of acceptability of Sports Related Concussion intervention using a structured questionnaire. Unit of measure is the score of participants acceptability questionnaire using Likert scale (1-5) 1- Not at all, 2 - A little bit, 3 - Somewhat, 4 - Quite a bit, 5 - Very much

    Measured: 1 year

  10. Acceptability from Clinician Perspective

    Clinician ratings of acceptability of the Sports Related Concussion intervention, using a structured questionnaire. Unit of measure is the score of clinicians acceptability questionnaire using Likert scale 1- Strongly disagree, 2 - Disagree, 3 - No opinion, 4 - Agree, 5 - Strongly agree

    Measured: 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Sep 2025
  2. Study start7 Nov 2025
  3. Primary completion16 Jun 2026 (estimated)
  4. Study completion16 Jul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
20 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07175753
Sponsor's protocol ID
I-0033
Acronym
SRC
Status last verified
Sep 2025
First submitted
21 Jul 2025
Last updated
18 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Sports Related Concussion, run by Life University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 12 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: enrolling by invitation, as of the sponsor's last update on 18 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of Participants Who Complete All Study Visits and Procedures (time frame: 1 year). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Dec 2025.

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