Actively Recruiting

Phase Not Applicable
Age: 65Years +
All Genders
NCT06441136

Characterizing the Impact of Presbyphonia on Social Interaction

Led by Matthew R. Hoffman · Updated on 2025-07-17

25

Participants Needed

1

Research Sites

85 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to determine if presbyphonia, or voice disorder caused by age-related change in the larynx, is associated with change in social interaction. This proposal investigates the impact of voice impairment in older adults on social interaction, loneliness, social disconnectedness, and depression. A series of questionnaires, voice assessments, and interviews will be performed to improve our understanding of how voice disorders affect older adults and how treatment of voice impairment with voice therapy may improve quality of life.

CONDITIONS

Official Title

Characterizing the Impact of Presbyphonia on Social Interaction

Who Can Participate

Age: 65Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of presbyphonia with presbylaryngis on videostroboscopy showing bilateral true vocal fold atrophy and normal vocal fold motion bilaterally
  • Ability to complete all questionnaires and voice assessment tasks
  • Normal to mild hearing loss in aided condition (with hearing aids)
Not Eligible

You will not qualify if you...

  • Liquid dysphagia or pneumonia within the last year
  • Presence of vocal fold lesion, scar, or motion impairment
  • Neurologic disorder affecting the voice
  • Montreal cognitive assessment score less than 26, or less than 25 if 12 or fewer years of formal education

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University of Iowa Hospitals & Clinics

Iowa City, Iowa, United States, 52242

Actively Recruiting

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Research Team

M

Matthew R Hoffman, MD, PhD

CONTACT

E

Emma L Thayer, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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