- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04310436
Modifying Unconscious Tongue Movements in Adults With Developmental Stammer.
Modifying Unconscious Tongue Movements to Improve Fluency in Adults With a Confirmed Developmental Stammer. A Pilot Randomised Feasibility Study.
Study Overview
Status
Conditions
Detailed Description
Participants will be assessed for stammering severity either on line via video link or in the Institute of Technology Sligo Health Science & Exercise Physiology Lab (B2004) at three time points: before intervention, after a five-week trial period and three months post completion. Participants will complete two assessments at each time to cater for "off" days. Participants will be required to practice quick eye movements at the start of words / syllables where dysfluencies are predicted for 10 minutes twice a day for the treatment period. Training in eye movement (saccade) modification will occur following the initial assessment in IT Sligo, or video link.
Participants will be assigned to one of two treatment arms. An experimental arm, and a control (placebo) arm. All participants will be assessed regarding their premonitory awareness of anticipated dysfluencies both before training and at the three month Based on advice from Community Speech and language Manager (Ms Sinead Carthy), participants will voice/video message the principle investigator once per week for this five-week period to confirm compliance.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Co Sligo
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Sligo, Co Sligo, Ireland, F91YW50
- Institute of Technology, Sligo
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Adults age > 18 years.
- A diagnosis of confirmed developmental stammer from SALT characterized by stammering on ≥ 3% of syllables.
- A proficiency in the English Language.
- No diagnosis of any emotional, behavioural, learning or neurological disorder.
- Cognitive ability to take part.
- Have previously completed a course of outpatient treatment for confirmed developmental stammer.
Exclusion Criteria:
- Younger than 18 years.
- Not having completed a traditional intervention for stammer.
- This research is not intended to replace current interventions but provide additional possibilities for those adults who have completed a standard programme of intervention and their developmental stammer still persists and a rate of ≥ 3% of syllables
Study Plan
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: Looking down to naval.
Modifying Saccade origin by looking down to naval.
|
Paragraphs from list Provided by Researcher.
Participants to read out loud for 10 minutes twice per day for the five week period.
On any word they anticipate / experience dysfluencies look quickly down to their naval to reset the lateral tongue position.
|
|
Placebo Comparator: Looking up in the air.
Modifying Saccade origin by looking up in the air.
|
Paragraphs from list provided by Researcher.
Participants to read out loud for 10 minutes twice per day for the five week period.
On any word they anticipate / experience dysfluencies look quickly up to reset the lateral tongue position.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stammering Severity (SSI-4) (Howell et. al. 2011).
Time Frame: 10 minutes.
|
Measures stuttering severity in adults and children.
It measures the percentage of stuttered syllables versus fluent speech in the participant.
It also measures the frequency of repetition and prolongations, duration of blocks, and physical concomitants.
|
10 minutes.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stammering Experience Overall Assessment of the Speaker's Experience of Stuttering OASES-A (Yaruss & Quesal 2006).
Time Frame: 10 minutes.
|
Measures the impact of stuttering on a person's life.
Scores range between 1 (Mild) and 5 (Severe).
The impact is broken down to four sections: General Information, Speaker's reactions, Daily Communication and Quality of life.
There is also an overall impact score.
|
10 minutes.
|
|
Premonitory Awareness in Stuttering Scale (PAiS) (Cholin et. al. 2016).
Time Frame: 10 minutes.
|
Measures the anticipation effect in stuttering.
14 items assessing premonitory awareness of stuttering sensation to assess the individual's capacity, manner and style of anticipation.
Each item consists of a 4-point Likert scale ranging from "not at all" to "very much".
A higher score indicates a larger anticipation of stuttering by the participant.
|
10 minutes.
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Hilary Mc Donagh, MSc, Study Principal Investigator
Study record dates
Study Major Dates
Study Start (Actual)
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
- ITSligo HMcD
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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