- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04813588
Comparison of Pantomiming and Easy Onset Treatment
March 21, 2021 updated by: Riphah International University
Comparison of Pantomiming and Easy Onset Treatment on Blocking in Stammering
This research will give in-depth understanding of pantomiming and easy onset method as an intervention of stuttering and especially blocking.
And by comparing both methods, It will also determine that which method is more effective.
This research will also improve the overall awareness regarding stuttering
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Research participants will be divided into two groups through randomization, Group A & Group B. Base line assessment will be conducted.
Intervention will be provided (thrice a week on alternative days).post
assessment will be taken and data will be analyzed through SPSS.
Study Type
Interventional
Enrollment (Anticipated)
20
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 Locations
-
-
Punjab
-
Rawalpindi, Punjab, Pakistan, 43600
- Recruiting
- Maryam Nadir Kiyani
-
Contact:
- Maryam Kiyani, MsSLP
- Email: maryam.Kiyani@riphah.edu.pk
-
Principal Investigator:
- Saba Imtiaz, MS/SLP
-
-
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
6 years to 18 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Participants falling in this category would be added into the study.
- School aged children and adolescents ages between 6 to 18 years(both genders) who stutter with blocking symptoms
- Participant who will be at moderate level of stammering will be included
Exclusion Criteria:
- Participant failing to fall in this category would be excluded of the study.
- Participants with any other medical condition will be excluded
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: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pantomimng
In experimental group pantomiming treatment will be administered
|
Pantomiming with fluency shaping techniques
|
|
Active Comparator: Easy onset
In active comparator group easy onset method will be administered
|
Easy onset method with breathing exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
The real time analysis
Time Frame: 12 weeks
|
Changes from base line "The Real time analysis will use.
It will use to assessed the changes in frequency ,duration types and severity of disfluencies in spontaneous speech.The total number of dysfluencies will be divided by the total number of syllables then multiply answer by 100 .Results between 2% showed normal range,8-15% will consider Moderate level, 12% will consider as severe level
|
12 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maryam Kiyani, MS/SLP, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Belyk M, Kraft SJ, Brown S. Stuttering as a trait or state - an ALE meta-analysis of neuroimaging studies. Eur J Neurosci. 2015 Jan;41(2):275-84. doi: 10.1111/ejn.12765. Epub 2014 Oct 28. Erratum In: Eur J Neurosci. 2017 Feb;45(4):622-624.
- 2. Mundada M, Gawali B, Kayte S. Recognition and classification of speech and its related fluency disorders. International Journal of Computer Science and Information Technologies (IJCSIT). 2014;5(5):6764-7.
- 3. Hudock D, Altieri N, Sun L, Bowers A, Keil C, Kalinowski J. The effect of single syllable silent reading and pantomime speech in varied syllable positions on stuttering frequency throughout utterance productions. Speech Communication. 2015 Dec 1;75:76-83.
- 4. Waghmare SD, Deshmukh RR, Shrishrimal PP, Waghmare VB, Janvale GB, Sonawane B. A Comparative Study of Recognition Technique Used for Development of Automatic Stuttered Speech Dysfluency Recognition System. Indian Journal of Science and Technology. 2017 Jul;10(21):1-4.
- Euler HA, Lange BP, Schroeder S, Neumann K. The effectiveness of stuttering treatments in Germany. J Fluency Disord. 2014 Mar;39:1-11. doi: 10.1016/j.jfludis.2014.01.002. Epub 2014 Jan 27.
- 6. Kordell J. Outcomes of a Combined Mindfulness, Stuttering Modification, and Fluency Shaping Intervention for Children Who Stutter
- 7. Keil CM, Hudock D, Altieri N, Seikel AT. The Effects of Pantomine Speech & Silent Reading in Varied Syllable Positions Throughout a Phrase on Stuttering
- 8. Rifaie NA, Saber AS, El-Din ST, Sallam YA, Algamal AM. Efficacy of the Arabic Modified Fluency Shaping Program in the treatment of stuttering. The Egyptian Journal of Otolaryngology. 2016 Oct 1;32(4):306.
- 9. Franklin CM. The Effect of Easy Onset Time Treatment on Voice Onset Time in Stuttering.
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)
March 1, 2021
Primary Completion (Anticipated)
May 1, 2021
Study Completion (Anticipated)
June 1, 2021
Study Registration Dates
First Submitted
February 16, 2021
First Submitted That Met QC Criteria
March 21, 2021
First Posted (Actual)
March 24, 2021
Study Record Updates
Last Update Posted (Actual)
March 24, 2021
Last Update Submitted That Met QC Criteria
March 21, 2021
Last Verified
March 1, 2021
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- REC/00897 Saba Imtiaz
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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