- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06266403
Evaluating Verbal Communication in Structured Interactions: Theoretical and Clinical Implications
The goal of this clinical trial is to learn about the effect of communicative interaction on verbal communication in people with amyotrophic lateral sclerosis (ALS) and age-matched speakers.
The question is, What are the effects of communicative interaction on verbal communication in people with ALS?
Participants will read words and sentences while they are in a solo setting and interactive setting.
Study Overview
Status
Conditions
Detailed Description
PALS and age-matched adults will participate in one solo speech production task (clear speech) and three interactive tasks (structured communicative interaction, unstructured communicative interaction, and clear speech structured communicative interaction) in which they work with an unfamiliar, naive interlocutor. This study is designed to examine the differences in speech produced in the four tasks. Comparisons of speech produced by PALS and age-matched adults will clarify whether differences in speech observed across the four tasks are a function of the speech difficulties experiences by PALS.
Plans for Assignment - This is a single group study in which all participants will engage in the same tasks.
Delivery of Intervention: Using tablets and audio recording devices provided to them, participants will complete this task in the comfort of their home. Study protocols will be explained via videoconferencing by experimenters. Produced speech will be recorded using solid-state audio recorders as well as remotely through the video conferencing software.
Adequacy of Sample size. Assuming medium effect sizes (Cohen's f = 0.3) based on our pilot data, for 80% power at an alpha of .05, the investigators will require 76 speakers. The investigators propose n = 100 PALS in order to account for speech variability that is common for PALS. The investigators plan to recruit 50 age-matched speakers. The investigators anticipate that this sample size will be sufficient to make appropriate comparison to the PALS group because there will be considerably less variability in these speakers.
Adequacy of Analyses. The proposed statistical analyses (Generalized mixed effects regressions) are standard and will be used to analyze the effect of the intervention on the outcome measures described below. Severity of condition (for PALS) will be included in the analyses and by-subject slopes and intercepts will be used to account for variability across participants.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Anne Olmstead, Ph.D.
- Phone Number: 814-867-3373
- Email: ajo150@psu.edu
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Speakers with ALS (PALS)
- diagnosis of ALS following the revised EL Escorial criteria
- no history of other neurological conditions (e.g., stroke)
- no cognitive impairment assessed by Telephone Montreal Cognitive Assessment (mini MoCA)
- detectable speech disturbance according to the ALS Functional Rating Scale-Revised (ALSFRS-R)
- the ability to produce single words
- being a native speaker of American English (AE).
Age-matched Speakers
- passing the remote hearing screening
- having no known speech, language, or neurological disorders per self-report
- no cognitive impairment assessed by Telephone Montreal Cognitive Assessment (mini MoCA)
- being a functionally native monolingual speaker of American English.
Unfamiliar Interlocutors
- passing the remote hearing screening
- having no known speech, language or neurological disorders per self-report
- being a native monolingual speaker of AE
- having no experience communicating with people with dysarthria
- being between the ages of 18 and 40.
Exclusion Criteria:
- None - if volunteer meets the inclusion criteria, then they will be enrolled
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: People with amyotrophic lateral sclerosis, age-matched speakers
People with ALS and age-matched speakers will participate in structured communicative interaction.
|
Two interlocutors, one with ALS and a typical, unfamiliar interlocutor or an age-matched speaker and a typical interlocutor, will work together.
On each trial, one of the interlocutors will be randomly chosen to be the "speaker" and the other will be the "listener".
Each participant in the pair will view the same set of words on their screens.
After one second, one of the words will be highlighted on the speaker's screen, they will say the word in the phrase "Click on the ____ this time", and the listener will click on it.
After the listener has made their selection, both participants will receive feedback on trial success.
PALS and age-matched speakers will read critical words consisting of target segments (e.g., "hid", "ship", "net") in random order four times.
These words will be embedded in the carrier phrase "Click on the ___ this time."
Participations will be instructed to overenunciate the critical words.
Two interlocutors, one with ALS and a typical, unfamiliar interlocutor or an age-matched speaker and a typical interlocutor, will work together.
The pairs will be presented with two different versions of the same picture with eight differences chosen to elicit the same target segments (e.g., "hid", "ship", "net").
These pictures will be modified from the LUCID corpus.
In total, pairs will complete four picture sets per session.
Pairs will be given 5 minutes for each picture set.
Two interlocutors, one with ALS and a typical, unfamiliar interlocutor or an age-matched speaker and a typical interlocutor, will work together.
On each trial, one of the interlocutors will be randomly chosen to be the "speaker" and the other will be the "listener".
Each participant in the pair will view the same set of words on their screens.
After one second, one of the words will be highlighted on the speaker's screen, they will say the word in the phrase "Click on the ____ this time", and the listener will click on it.
The speaker will be instructed to overenunciate the critical words.
After the listener has made their selection, both participants will receive feedback on trial success.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Formant frequencies of speech sounds
Time Frame: two 60 minute sessions
|
Formant frequencies that characterize speech sounds will be made on speech recorded in the intervention task.
|
two 60 minute sessions
|
Intelligibility of recorded speech
Time Frame: two 60 minute sessions
|
Perceptual judgments will be provided by solo, naïve listeners who did not participate in the interactions.
Listeners will hear recorded speech of PALS and age-matched speakers recorded across the different tasks and indicate what they heard.
The score will be expressed in percent.
The possible range is between 0-100%.
The higher scores mean a better outcome.
|
two 60 minute sessions
|
Syntactic properties
Time Frame: One 60 minute session
|
Syntactic complexity in the unstructured communication task will be measured through mean length of grammatical units, clausal density, and clause type.
Each variable will be assessed at both the dyadic level (e.g., clausal density for both interlocutors together) and at the level of the individual speaker (e.g., clausal density of each speaker).
A composite of these measures will provide an index of the syntactic complexity of the conversation.
|
One 60 minute session
|
Pragmatic Properties
Time Frame: One 60 minute session
|
The investigators will count the number and duration of silent portions of speech, filled pauses, linguistic mazes, speaking turns, and interruptions in the unstructured communication task. A composite measure of the individual measures will provide an index of an individual's contribution to the conversation. |
One 60 minute session
|
Duration of speech sounds
Time Frame: two 60 minute sessions
|
Durations that characterize speech sounds will be made on speech recorded in the intervention task.
|
two 60 minute sessions
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jimin Lee, PhD, The Pennsylvania State University
- Principal Investigator: Navin Viswanathan, PhD, The Pennsylvania State University
- Principal Investigator: Anne Olmstead, PhD, The Pennsylvania State University
Publications and helpful links
General Publications
- Olmstead AJ, Lee J, Viswanathan N. The Role of the Speaker, the Listener, and Their Joint Contributions During Communicative Interactions: A Tripartite View of Intelligibility in Individuals With Dysarthria. J Speech Lang Hear Res. 2020 Apr 27;63(4):1106-1114. doi: 10.1044/2020_JSLHR-19-00233. Epub 2020 Apr 17.
- Olmstead, A. J., Viswanathan, N., Cowan, T., & Yang, K. (2021). Phonetic adaptation in interlocutors with mismatched language backgrounds: A case for a phonetic synergy account. Journal of Phonetics, 87, 101054.
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- STUDY00024154
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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