NCT07175753

Brief 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 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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
20

participants targeted

Target at below P25 for all trials

Timeline
2mo left

Started Nov 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress72%
Nov 2025Jul 2026

First Submitted

Initial submission to the registry

July 21, 2025

Completed
2 months until next milestone

First Posted

Study publicly available on registry

September 16, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

November 7, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 16, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 16, 2026

Last Updated

December 18, 2025

Status Verified

September 1, 2025

Enrollment Period

7 months

First QC Date

July 21, 2025

Last Update Submit

December 10, 2025

Conditions

Keywords

Sports related concussionChiropractic clinical care

Outcome Measures

Primary Outcomes (4)

  • 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.

    1 year

  • Recruitment

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

    1 year

  • Retention

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

    1 year

  • Adherence

    Number of completed required study visits and treatments per participant.

    1 year

Secondary Outcomes (10)

  • Change in Executive Function, Attention, and Inhibitory Control

    1 year

  • Change in Visual Processing Speed

    1 year

  • Change in Fine Motor Skills and Dexterity

    1 year

  • Change in Postural Stability and Balance

    1 year

  • Change in Auditory Processing and Speech Recognition in Noise

    1 year

  • +5 more secondary outcomes

Study Arms (1)

SRC Group

Those who have sport-related concussion symptoms such as headache, nausea, dizziness, loss of consciousness, amnesia, balance impairment, irritability, visual disturbance, slow reaction times, etc.

Other: chiropractic applied clinical neuroscience care

Interventions

Standard chiropractic care with physiotherapy and phototherapy over two sessions

SRC Group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)
Sampling MethodNon-Probability Sample
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.

You may qualify if:

  • 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
  • Loss of consciousness
  • Amnesia
  • Balance impairment
  • Irritability
  • Visual disturbance
  • Slowed reaction times

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

NeuroLife Institute

Marietta, Georgia, 30060, United States

Location

Study Officials

  • Taha Begum, MBBS, PhD

    Life University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 21, 2025

First Posted

September 16, 2025

Study Start

November 7, 2025

Primary Completion (Estimated)

June 16, 2026

Study Completion (Estimated)

July 16, 2026

Last Updated

December 18, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations