Actively Recruiting

Phase Not Applicable
Age: 16Years - 65Years
All Genders
ID07176988

Deconstructing Voice Therapy: Towards Enhanced Communication Outcomes

Led by Emory University · Updated on 2025-10-20

120

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

E

Emory University

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating different methods of voice therapy to improve speech outcomes over 12 months in people with voice problems, specifically those diagnosed with primary muscle tension dysphonia (MTD) or benign vocal fold lesions. The study also explores how clear speech relates to vocal characteristics and patient-reported outcomes, as well as the connection between overall voice improvement and the use of clear speech. The study compares two approaches to voice therapy: a traditional hierarchical method and a new non-hierarchical Conversation Training Therapy (CTT). The hierarchical method involves four weekly sessions starting with simple sounds and progressing to full conversations, requiring mastery of each step before moving on. The non-hierarchical method also has four weekly sessions but introduces techniques like clear speech, awareness training, and embedded gestures in a flexible order, supported by daily practice using a mobile app. Participants will attend therapy sessions and follow-up visits over a year, during which voice outcomes are measured through questionnaires, acoustic tests, and laryngeal imaging at multiple time points. Researchers will track changes in voice handicap scores, vowel sounds, voice severity, vocal fold function, airflow, and adherence to therapy. The study aims to understand how these therapy methods affect voice quality and communication over time.

CONDITIONS

Brief Title

Deconstructing Voice Therapy: Towards Enhanced Communication Outcomes

Who Can Participate

Age: 16Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Non-smoking
  • Diagnosis of primary muscle tension dysphonia (hyperadducted type) or benign vocal fold lesions
  • No neuro-laryngologic or age-related vocal fold changes
  • No voice therapy or voice surgery in the last year
  • No serious chronic medical conditions affecting voice
  • Normal hearing as determined by pure tone audiometry
  • Suitable for behavioral voice intervention as determined by specialists
  • Willing to attend all therapy and follow-up sessions
  • Willing to use a smartphone to record practice
Not Eligible

You will not qualify if you...

  • History of voice therapy or voice surgery in the last year
  • Serious chronic medical condition affecting voice
  • Abnormal hearing despite amplification
  • Other laryngeal disorders not due to primary MTD or benign lesions
  • Not suitable for behavioral voice intervention as determined by specialists
  • Unwilling to attend therapy and follow-up sessions
  • Unwilling to use a smartphone to record practice
  • Pregnant women
  • Prisoners
  • Cognitive impairment or impaired decision-making capacity

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive behavioral voice therapy using either a hierarchical or non-hierarchical Conversation Training Therapy method. Therapy consists of four weekly sessions focused on improving voice use, with daily practice using a mobile app.

4 weekly visits (in-person) plus daily at-home practice

Follow-up

Duration - Up to 12 months post treatment

Participants are monitored for voice improvements and therapy adherence at multiple points after treatment to assess long-term outcomes.

Visits at 1 week, 3 months, 6 months, and 12 months post treatment

Trial Site Locations

Total: 1 location

1

Emory Voice Center at Emory University Hospital Midtown

Atlanta, Georgia, United States, 30308

Actively Recruiting

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Research Team

A

Amanda Gillespie, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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