Association of History of Concussion With Vestibular Impairment and Cognitive Function in Sports Athletes

March 25, 2024 updated by: Riphah International University
This study investigates the potential relationship between prior concussions and their impact on both vestibular function and cognitive abilities in athletes participating in sports.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

The association of a history of concussions with vestibular impairment and cognitive function in sports athletes is a significant area of research due to the potential long-term consequences of head injuries in contact sports.

Vestibular impairment refers to disruptions in the balance and spatial orientation system of the inner ear, which can result from head trauma. Cognitive function encompasses various mental processes, including memory, attention, and decision-making, which may be affected by concussions.

This study aims to examine how prior concussions relate to both vestibular impairment and cognitive function in athletes participating in sports. Researchers typically employ a combination of self-reported concussion history, clinical assessments of vestibular function, and standardized cognitive tests to evaluate participants.

Findings from such studies can provide valuable insights into the potential effects of concussions on athletes' balance, spatial awareness, and cognitive abilities. Understanding these associations can inform concussion management protocols, rehabilitation strategies, and preventive measures in sports settings.

Furthermore, this research may contribute to the development of targeted interventions aimed at improving vestibular rehabilitation and cognitive training for athletes with a history of concussions. By identifying and addressing these potential deficits early, athletes may reduce their risk of long-term complications and optimize their performance and well-being in sports.

Study Type

Observational

Enrollment (Estimated)

115

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Pakistan
    • Khyber Pakhtun Khawan
      • Peshawar, Khyber Pakhtun Khawan, Pakistan, 24730
        • Recruiting
        • Hayatabad Sports Complex
        • Contact:
        • Contact:
          • MAHEEN GUL, MSSPT*
          • Phone Number: +923319533510
        • Principal Investigator:
          • Maheen Gul, MS*SPT

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

N/A

Sampling Method

Probability Sample

Study Population

This includes information such as age, gender, and ethnicity of the athletes. Understanding the demographics of the population helps in assessing the generalizability of the study findings across different groups.

The number, severity, and timing of previous concussions experienced by each athlete. This helps in stratifying the participants based on concussion history and assessing potential cumulative effects.

Pre-existing medical conditions, history of previous injuries (e.g., musculoskeletal injuries), and baseline cognitive and physical performance measures. This information allows for controlling potential confounding variables and assessing the impact of concussion independently.

Description

Inclusion Criteria:

  • athletes actively involved in sports at age of 18 to 35
  • active players in contact sports

Exclusion Criteria:

  • Concussion other than sports
  • History of recent fractures.
  • Participants having neurological deficits

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
concussed contact sports athlete

Informed Consent: Participants are provided with information about the study, including its purpose, procedures, potential risks, and benefits. They are given the opportunity to ask questions and provide informed consent before participating.

Baseline Assessments: Before any interventions or assessments, participants undergo baseline evaluations of their vestibular function and cognitive abilities. This helps establish a starting point for comparison and allows researchers to identify any pre-existing impairments.

Concussion History Questionnaires: Participants complete questionnaires or interviews to provide detailed information about their history of concussions, including the number, severity, and timing of each injury.
Other: find association between vestibular impairment , cognitive fiunction with concussin
SCOAT 6 is a standardized tool used for evaluating athletes suspected of having a concussion. It includes a variety of components such as symptom evaluation, cognitive assessment, balance evaluation, and a neck examination. it helps in assessing the severity of the injury, tracking recovery, and making return-to-play decisions. Dr. Robert Cantu, a prominent figure in sports concussion research, has proposed guidelines for the management of concussions. These guidelines typically involve recommendations for the evaluation, treatment, and return-to-play decisions for athletes who have sustained concussions
Other Names:
  • identify concussion and find asociation through scoat 6 ad Cantu

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
CANTU
Time Frame: 3 DAYS
The Cantu guidelines, named after Dr. Robert Cantu, are a set of recommendations for the management of concussions in sports. Dr. Cantu, a renowned neurosurgeon and concussion expert, has contributed significantly to the understanding and treatment of concussions, particularly in the field of sports medicine. While there isn't a single document titled "Cantu Description," Dr. Cantu's work encompasses various aspects of concussion management, including diagnosis, treatment, and return-to-play protocols.
3 DAYS
Sports concussion office assesment tool 6
Time Frame: 3-30days
SCOAT 6 is a standardized tool used for evaluating athletes suspected of having a concussion. It includes a variety of components such as symptom evaluation, cognitive assessment, balance evaluation, and a neck examination. it helps in assessing the severity of the injury, tracking recovery, and making return-to-play decisions.
3-30days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Riphah International University

Investigators

  • Principal Investigator: Maheen gul, MSSPT*, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 23, 2024

Primary Completion (Estimated)

April 23, 2024

Study Completion (Estimated)

June 2, 2024

Study Registration Dates

First Submitted

March 25, 2024

First Submitted That Met QC Criteria

March 25, 2024

First Posted (Actual)

April 1, 2024

Study Record Updates

Last Update Posted (Actual)

April 1, 2024

Last Update Submitted That Met QC Criteria

March 25, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • REC/MS-PT/01832

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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