Masticatory Side-switch and Mixing Ability.

NCT05173259 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2022-11-03

No results posted yet for this study

Summary

The main aim of this cross-over intervention study is to assess the effect of masticatory side-switch frequency on different aspects of masticatory function, including masticatory mixing ability and rhythm. A secondary aim is to explore the subjective perception of taste, muscular fatigue, and saliva production through a VAS. Thirty-six volunteers recruited for convenience, among students of the Degree of Dentistry of the Faculty of Medicine and Health Sciences of the University of Barcelona, will perform 6 tests, each consisting of 2 assays, chewing a two-coloured chewing gum, during 40 masticatory cycles. The tests will be randomised masticatory sequences of "free-style", "unilateral-right", "unilateral-left", switching the chewing side at 5% "G05", at 15% "G15" and at 25% "G25". Video recordings of these tests will be made to later assess, on slow playback, the change of the chewing side and the masticatory rhythm. The masticatory mixing ability will be determined through the scanning and posterior analysis of the red-channel in the histogram plug-in in "ImageJ" (R).

Conditions

  • Chewing Problem
  • Mastication Disorder

Interventions

BEHAVIORAL

F

The participant will be asked to chew the two-coloured chewing gum naturally.

BEHAVIORAL

R

The participant will be asked to chew the two-coloured chewing gum on the right-side.

BEHAVIORAL

L

The participant will be asked to chew the two-coloured chewing gum on the left-side.

BEHAVIORAL

G05

The participant will be asked to chew the two-coloured chewing gum changing the side in 5%.

BEHAVIORAL

G15

The participant will be asked to chew the two-coloured chewing gum changing the side in 15%.

BEHAVIORAL

G25

The participant will be asked to chew the two-coloured chewing gum changing the side in 25%.

Sponsors & Collaborators

  • University of Barcelona

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-12-01
Primary Completion
2022-03-31
Completion
2022-09-28

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05173259 on ClinicalTrials.gov