The Test of Mastication and Swallowing Solids and the Timed Water Swallow Test

Sponsor
University of Haifa (Other)
Overall Status
Completed
CT.gov ID
NCT05132452
Collaborator
(none)
298
34.7

Study Details

Study Description

Brief Summary

This study aimed to gather more information regarding two clinically relevant tests: The Test of Mastication and Swallowing Solids (TOMASS) and the Timed Water Swallow Test (TWST). Both tests can be used clinically as part of swallowing disorders evaluation.

The aims of the study were to assess the reliability of the two tests, to document the effects of age and gender on the outcome measures of the TOMASS and TWST and to explore the relationship between participants' function in the two tests. To do that, 298 healthy participants were included. All of them did not have dysphagia. Most of them were elderly.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: The Test of Mastication and Swallowing Solids (TOMASS) and the Timed Water Swallow Test (TWST)

Detailed Description

Background: Quantitative measures of swallowing function can increase accuracy, reliability, and improve clinical decision making. The Test of Mastication and Swallowing Solids (TOMASS) and the Timed Water Swallow Test (TWST) are functional tests of swallowing that provide quantitative results.

Objectives: To explore the relationship between TOMASS and TWST; evaluate test-retest and interrater reliability; explore age and gender effects; and to gather normative data.

Methods: Healthy community dwelling participants (n = 298, ≥20 years old) were recruited. Of those, 126 were included in the reliability study. Participants completed the TWST and TOMASS.

Study Design

Study Type:
Observational
Actual Enrollment :
298 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Test of Mastication and Swallowing Solids and the Timed Water Swallow Test: Reliability, Associations, Age and Gender Effects, and Normative Data
Actual Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Dec 23, 2018
Actual Study Completion Date :
Dec 23, 2018

Arms and Interventions

Arm Intervention/Treatment
adults living in the community

Healthy community dwelling participants, aged 20 year old and above, without dysphagia.

Diagnostic Test: The Test of Mastication and Swallowing Solids (TOMASS) and the Timed Water Swallow Test (TWST)
Participants swallowed one cracker for the TOMASS. They swallowed 150 mL of water for the TWST.

Outcome Measures

Primary Outcome Measures

  1. duration [one-off assessment]

    length of time required to complete the task

  2. swallows [one-off assessment]

    number of swallows required to complete the task

  3. bites [one-off assessment]

    number of bites required to eat the cracker

  4. masticatory cycles [one-off assessment]

    number of masticatory cycles required to eat the cracker

  5. volume [one-off assessment]

    the amount of water swallowed

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • all participants were eligible to participate if they were over 20 years of age, with no known medical history of dysphagia, had an SDQ score of less than 11, indicating no suspicion for dysphagia, were able to give a written informed consent, and could follow simple verbal instructions. In addition, all participants indicated that they do not avoid eating crackers due to swallowing disorders or allergies.
Exclusion Criteria:
  • SDQ over 11 or medically reported dysphagia not eating crackers due to swallowing difficulty allergy to gluten

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Haifa

Investigators

  • Principal Investigator: oshrat sella, PhD, University of Haifa

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Oshrat Sella, Principal Investigator, University of Haifa
ClinicalTrials.gov Identifier:
NCT05132452
Other Study ID Numbers:
  • 1012
First Posted:
Nov 24, 2021
Last Update Posted:
Nov 24, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 24, 2021