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Comparison of Pantomiming and Easy Onset Treatment

Comparison of Pantomiming and Easy Onset Treatment on Blocking in Stammering

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04813588
Enrollment
20
Registered
2021-03-24
Start date
2021-03-01
Completion date
2021-06-01
Last updated
2021-03-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stammering

Keywords

Pantomiming, Easy onset method, Blocking

Brief summary

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

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.

Interventions

OTHERPantomiming

Pantomiming with fluency shaping techniques

OTHEREasy onset

Easy onset method with breathing exercises

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

RCT

Eligibility

Sex/Gender
ALL
Age
6 Years to 18 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The real time analysis12 weeksChanges 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

Countries

Pakistan

Contacts

Primary ContactImran Amjad, Phd
imran.amjad@riphah.edu.pk03324390125

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 12, 2026