Comparison of Pantomiming and Easy Onset Treatment
- Conditions
- Stammering
- Interventions
- Other: Easy onsetOther: Pantomiming
- Registration Number
- NCT04813588
- Lead Sponsor
- Riphah International University
- 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
- 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
- Participant failing to fall in this category would be excluded of the study.
- Participants with any other medical condition will be excluded
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Easy onset Easy onset In active comparator group easy onset method will be administered Pantomimng Pantomiming In experimental group pantomiming treatment will be administered
- Primary Outcome Measures
Name Time Method The real time analysis 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
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Maryam Nadir Kiyani
🇵🇰Rawalpindi, Punjab, Pakistan