Optimal Method for Tongue Strengthening

NCT04809558 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 87

Last updated 2023-11-22

No results posted yet for this study

Summary

The research team will conduct a multi-site, randomized controlled trial examining the effectiveness of exercise intensity progression compared to standard practice (no progression) in the context of swallowing rehabilitation. The study will also determine the impact of using biofeedback during resistance training on tongue strength. The study is a first step in determining an optimal delivery of tongue strengthening exercise in typically aging older persons, with the plan to develop a framework for guiding clinical practice of tongue strengthening in various dysphagic populations. Participants will be randomized into one of four treatment groups and complete 8 weeks of tongue resistance training.

Conditions

  • Focus of Study is Tongue Strength

Interventions

BEHAVIORAL

Tongue resistance exercise

Participant will complete tongue resistance exercises.

Sponsors & Collaborators

  • Case Western Reserve University

    collaborator OTHER
  • Emerson College

    collaborator OTHER
  • James Madison University

    collaborator OTHER
  • Texas Christian University

    collaborator OTHER
  • Samford University

    lead OTHER

Principal Investigators

  • Sarah H Szynkiewicz, Ph.D. · Samford University

  • Erin Kamarunas, Ph.D. · James Madison University

  • Teresa Drulia, Ph.D. · Texas Christian University

  • Lindsay Griffin, Ph.D. · Emerson College

  • Rachel Mulheren, Ph.D. · Case Western Reserve University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-06-01
Primary Completion
2022-08-15
Completion
2022-08-15

Countries

  • United States

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 NCT04809558 on ClinicalTrials.gov