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Clinical Trials/NCT03129880
NCT03129880
Completed
Not Applicable

Voice-related Outcomes in Response to Intensive Versus Traditional Therapy Programs

University of Wisconsin, Madison1 site in 1 country15 target enrollmentMarch 13, 2016
ConditionsDysphonia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dysphonia
Sponsor
University of Wisconsin, Madison
Enrollment
15
Locations
1
Primary Endpoint
Self-efficacy and readiness scale Changes
Status
Completed
Last Updated
last year

Overview

Brief Summary

The purpose of this study is to determine if there are differences in treatment outcomes between traditional voice therapy, performed weekly for a maximum of 6 weeks versus intensive voice therapy, consisting of 4-6 therapy sessions performed within one day.

Detailed Description

The goal of voice therapy is optimal long-term vocal quality and communication function with minimal recurrence. Traditional voice therapy for dysphonia typically consists of one to two therapy sessions each week with a single clinician for about 8 weeks. Another approach of voice therapy is intensive short-term therapy also known as "boot camp." This approach, borrows from the disciplines of neurobiology, exercise physiology, motor learning, and psychotherapy which describe desirable learning and behavior changes influenced by practice that involves high-intensity overload, variability, and specificity of training. A few studies have showed that "Boot Camp" model of intensive therapy resulted in comparable gains in voice quality and vibratory mechanics and may promote better patient satisfaction and attendance. While such findings support the notion that intensive voice therapy may enhance voice therapy outcomes, no study to date has examined patient response to the "Boot Camp" approach to voice therapy. The investigators will compare the outcomes of traditional, weekly voice therapy and intensive voice therapy with multiple sessions in one day.

Registry
clinicaltrials.gov
Start Date
March 13, 2016
End Date
March 12, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with a Voice disorder
  • Diagnosed with benign vocal fold lesions and/or hyper-function
  • First/primary propose treatment modality is voice therapy
  • Patients who are appropriate for either standard of care treatment modality (traditional or intensive voice therapy)
  • Willingness to participate in either standard of care treatment modality
  • All races
  • Males and females
  • English speaking

Exclusion Criteria

  • Younger than 18
  • Inability or unwillingness to participate in one of the standard of care treatment modalities
  • Laryngeal Surgery or procedures during course of study
  • Prisoners

Outcomes

Primary Outcomes

Self-efficacy and readiness scale Changes

Time Frame: Baseline compared to Immediately post voice therapy

Pre to Post difference in participant's self-efficacy for voice practice and healthy voice technique between therapy groups and within subsets of subjects - readiness ruler of 0 (not at all) to 10 (extremely)

Self-efficacy and readiness scale Change

Time Frame: Baseline compared to 12 weeks post voice therapy

Pre to Post difference in participant's self-efficacy for voice practice and healthy voice technique between therapy groups and within subsets of subjects - readiness ruler of 0 (not at all) to 10 (extremely)

Study Sites (1)

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