NCT07366216

Brief Summary

This study aims to investigate the effects of visual, auditory, and motor dual-task conditions on chewing performance in individuals with multiple sclerosis, compared with healthy controls.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
48

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

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

First Submitted

Initial submission to the registry

January 9, 2026

Completed
17 days until next milestone

First Posted

Study publicly available on registry

January 26, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

January 26, 2026

Completed
20 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 15, 2026

Completed
14 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2026

Completed
Last Updated

January 26, 2026

Status Verified

January 1, 2026

Enrollment Period

20 days

First QC Date

January 9, 2026

Last Update Submit

January 16, 2026

Conditions

Outcome Measures

Primary Outcomes (5)

  • Test of Masticating and Swallowing Solids

    Test of Masticating and Swallowing Solids (TOMASS) is a standardized clinical assessment used to evaluate solid bolus mastication and swallowing performance.

    Baseline (single-task and dual-task conditions assessed on the same day)

  • Mini-Mental State Examination (MMSE)

    The MMSE is a brief, widely used screening tool for assessing global cognitive function.

    Baseline

  • Go/No-Go Test

    The Go/No-Go Test is a neuropsychological assessment used to evaluate response inhibition and sustained attention.

    Baseline (single-task and dual-task conditions assessed on the same day)

  • Auditory Reaction Time Test

    The Auditory Reaction Time Test is used to assess auditory attention and the speed of motor response to auditory stimuli.

    Baseline (single-task and dual-task conditions assessed on the same day)

  • Tap Tool

    The Tap Tool is a neuropsychological and motor performance assessment used to evaluate psychomotor speed and fine motor control.

    Baseline (single-task and dual-task conditions assessed on the same day)

Study Arms (2)

Multiple Sclerosis

Healthy Control

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consisted of individuals with multiple sclerosis and age-matched healthy controls.

You may qualify if:

  • Individuals aged between 18 and 65 years
  • Mini-Mental State Examination (MMSE) score of 24 or higher
  • Right-hand dominance

You may not qualify if:

  • Presence of visual and/or hearing impairment
  • Presence of difficulties in solid food intake and/or complaints related to mastication
  • Presence of neurological, psychological, cognitive, and/or chronic conditions that may affect mastication or chewing function
  • History of interventions affecting oral structure (e.g., oral/maxillofacial surgery or radiotherapy) within the last month
  • Known allergy to the food used in the test

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ondokuz Mayis University

Samsun, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Multiple Sclerosis

Condition Hierarchy (Ancestors)

Demyelinating Autoimmune Diseases, CNSAutoimmune Diseases of the Nervous SystemNervous System DiseasesDemyelinating DiseasesAutoimmune DiseasesImmune System Diseases

Central Study Contacts

Seda Nur Kemer, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
CROSS SECTIONAL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator, PT, PhD

Study Record Dates

First Submitted

January 9, 2026

First Posted

January 26, 2026

Study Start

January 26, 2026

Primary Completion

February 15, 2026

Study Completion

March 1, 2026

Last Updated

January 26, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations