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Not yet recruiting NCT06996470

The Relationship Between Cervical Endurance Time and Eye Gaze

— Observational Endurance Time During Gazing

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: - Cervical Vestibular-Evoked Myogenic Potential (cVEMP) along the Sternocleidomastoid.
Who it may be relevant to
Registry conditions: Endurance Time During Gazing. Basic parameters: 18 years — 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

The Relationship Between Cervical Endurance Time and Eye Gaze Dual Time in University Students

Overview

46 normal students will participate at the study; they will be randomly divided (male and female) into 2 groups (23 for each group) The study will be conducted in physical therapy lab and Speech and hearing center at Allied medical school.

Interventions

  • Other - Cervical Vestibular-Evoked Myogenic Potential (cVEMP) along the Sternocleidomastoid
    Endurance time during gazing

Primary outcome measures

  • Endurance time during gazing [Time frame: at base line]
  • Endurance time without gazing gazing [Time frame: at base line]
  • Attention Span Scale for Students [Time frame: at base line]
  • Cervical Vestibular-Evoked Myogenic Potential (cVEMP) [Time frame: at base line]

Eligibility criteria

Inclusion criteria

  • Normal students

Exclusion criteria

  • subjects achieving less than 20 mmHg in the CCFT test
  • Students with cervical pain within the last six months

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06996470 · 1979

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗