- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06815263
Listener Training for Improved Intelligibility of People With Parkinson's Disease
April 22, 2026 updated by: Utah State University
Listener training offers a promising avenue for improving communication for people with dysarthria due to Parkinson's disease by offsetting the intelligibility burden from the patient onto their primary communication partners.
Here, we employ a repeated-measures, randomized controlled trial to establish the efficacy of listener training for patients with PD and their primary communication partners.
This translational work will establish a new realm of clinical practice in which the intelligibility impairments in PD are addressed by training partners to better understand dysarthric speech, thus elevating communication outcomes and participation in daily life.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
People with dysarthria due to Parkinson's disease (PD) frequently present with reduced intelligibility, which can have significant consequences, including reduced participation in situations involving communicating with others and resulting in social isolation.1-5
Few effective treatments exist to ease the intelligibility burden of dysarthria in PD, and most require significant cognitive and physical effort on the part of the speaker to achieve and maintain gains.6,7
Once people with PD have progressed beyond the early stages of the disease, and their cognitive and physical impairments limit their ability to use traditional speech therapy techniques, they are not realistic treatment candidates for current interventions; and no other interventions are available to support their communication.
This is a serious and consequential gap in clinical care for people with PD.
The current proposal addresses this critical gap by shifting the weight of behavioral change from the speaker to the listener, specifically key communication partners such as family.
Indeed, for older adults, most of their time spent with others is spent with family members.8
Further, key partners of patients with PD wish to have a more significant and active role in communication rehabilitation.9,10
A listener-targeted remediation approach for intelligibility impairments in people with dysarthria and PD is firmly grounded in theoretical models of perceptual learning11-13 and rigorously supported by our decade-long research program targeting perceptual learning of dysarthric speech.14-30
To date, this line of investigation has chiefly targeted the theory of listener adaptation to the degraded signal; however, robust intelligibility improvements of up to 20 percent across studies have been observed.15
With a rigorous account of how and what listeners adapt to, we are ideally positioned to move this work from bench to bedside, establishing listener (i.e., perceptual) training as a clinical intervention to improve intelligibility in people with PD.
Here, we establish the efficacy of listener training for patients with PD and their primary communication partners using a repeated-measures, randomized controlled trial (SA1).
Immediate acquisition and retention of intelligibility improvements will be examined as a function of speaker severity.
We then evaluate three theoretically and empirically-motivated communication benefits of listener training that extend beyond intelligibility, including listening effort, comprehension, and communicative participation (SA2).
Finally, we engage stakeholder input to inform clinical implementation of listener training using qualitative semi-structured interviews (SA3) with patients with PD and their partners.
This will provide insights into the effectiveness and feasibility of the intervention approach, ensuring that their needs and preferences are considered and that they feel empowered and motivated for a listener training approach.
Thus, in three independent aims, this proposal will address a current void in our clinical toolbox, establishing a new realm of clinical practice in which communication challenges in PD are managed by training partners to better understand the degraded speech.
Study Type
Interventional
Enrollment (Estimated)
360
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Stephanie Borrie, PhD
- Phone Number: 435-797-1388
- Email: stephanie.borrie@usu.edu
Study Contact Backup
- Name: Morgan Robertson, PhD
- Phone Number: 435-797-1388
- Email: morgan.robertson@usu.edu
Study Locations
-
-
Florida
-
Tallahassee, Florida, United States, 32306
- Recruiting
- Florida State University
-
Contact:
- Kaitlin Lansford, PhD
- Phone Number: 850-644-8443
- Email: klansford@fsu.edu
-
Principal Investigator:
- Kaitlin Lansford, PhD
-
-
Utah
-
Logan, Utah, United States, 43221
- Recruiting
- Utah State University
-
Contact:
- Stephanie Borrie, PhD
- Phone Number: 435-797-1388
- Email: stephanie.borrie@usu.edu
-
Principal Investigator:
- Stephanie Borrie, PhD
-
Sub-Investigator:
- Sarah Leopold, PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- Primary language is English
- 18 years or older
- medical diagnosis of Parkinson's disease (patient participants)
- speech diagnosis of hyperkinetic dysarthria, exhibiting hallmark characteristics (patient participants)
Exclusion Criteria:
- Severe cognitive impairment
- Less than 18 years of age
- Primary language other than English
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Condition
Listener receives speech of patient with dysarthria
|
Partner participants are presented with individual audio phrases that make up passage reading speech stimuli and orthographic transcriptions of what the patient is saying.
Partners are asked to listen carefully to the audio files and use the written subtitles to help them understand what is being said.
|
|
Sham Comparator: Control condition
Listener receives speech of speaker with no speech disorder
|
Partner participants are presented with individual audio phrases that make up passage reading speech stimuli and orthographic transcriptions of what the patient is saying.
Partners are asked to listen carefully to the audio files and use the written subtitles to help them understand what is being said.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Speech intelligibility
Time Frame: pretest, during training, immediate posttest, one week posttest, one month posttest
|
Percent words correct (PWC)
|
pretest, during training, immediate posttest, one week posttest, one month posttest
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Communicative Participation Item Bank
Time Frame: Pretest, one month posttest
|
Patient and partner reported summed score across different communication situations
|
Pretest, one month posttest
|
|
Listening effort
Time Frame: Pretest, one week posttest, one month posttest
|
Rating scale, 0-100 scale with question "how easy is this speech to understand", with endpoints of 'difficult' on the zero side and 'easy' on the 100 side
|
Pretest, one week posttest, one month posttest
|
|
Comprehension
Time Frame: Pretest, one week posttest, one month posttest
|
Story comprehension accuracy score, listeners answer a series of multiple choice comprehension questions, accuracy is defined as how many correct responses they choose for each story
|
Pretest, one week posttest, one month posttest
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Stephanie Borrie, PhD, Utah State University
- Principal Investigator: Kaitlin Lansford, PhD, Florida State University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
April 7, 2025
Primary Completion (Estimated)
January 1, 2029
Study Completion (Estimated)
May 1, 2029
Study Registration Dates
First Submitted
February 3, 2025
First Submitted That Met QC Criteria
February 3, 2025
First Posted (Actual)
February 7, 2025
Study Record Updates
Last Update Posted (Actual)
April 23, 2026
Last Update Submitted That Met QC Criteria
April 22, 2026
Last Verified
April 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14004 (City of Hope Medical Center)
- 1R01DC020930 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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