- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07058246
- Original Trial
Effectiveness of Mime Therapy vs Conventional Therapy for Bell's Palsy
Effectiveness of Mime Therapy and Conventional Therapy for the Patients of Bell's Palsy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab
-
Gujranwala, Punjab, Pakistan, 52250
- Al Raee Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Patient diagnosed with acute bell's palsy
- All genders and intact taste sensations
- No other neurological deficit involving face
Exclusion Criteria:
- Uncontrolled hypertension
- Stroke patients
- Patient with mental and dental implants
- Patient with recurrent facial palsy
- Patient with tumors, congenital defects, open wound
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: Group A
Group A is the experimental group having 17 participants randomly chosen by using coin toss method according to inclusion and exclusion criteria. Baseline Treatment include DL2 electric stimulation at 20-50Hz for 90 repetitions and Infrared lamp placed 30-45cm away from the body for 10-15 minutes. Mime Therapy along with Conventional Therapy. |
Experimental group was given mime therapy along with conventional therapy. Mirror therapy, Raising eyebrows as if surprised, Widening eyes in shock, blinking rapidly, Extreme smiling, Eye closure with dramatic expressions, exaggeration nose wrinkling. pouting and mouth opening, expression transitions. Total sessions given are 4-5 per week in 3 weeks consist of 45 mins. Number of repetitions are 5-10 with the hold of 5 second x 2 sets. |
|
Active Comparator: Group B
Group B is the active comparator group having 17 participants randomly chosen by using coin toss method according to inclusion and exclusion criteria. Baseline Treatment include DL2 electric stimulation at 20-50Hz for 90 repetitions and Infrared lamp placed 30-45cm away from the body for 10-15 minutes. Conventional Therapy. |
Raising and lowering eyebrows, Wrinkling nose, smiling, frowning, massage. Total sessions given are 4-5 per week in 3 weeks consist of 45 mins. Number of repetitions are 5-10 with the hold of 5 second x 2 sets. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Facial Disability Index
Time Frame: 4 months
|
it includes physical well being scale which consist of 5 questions with a 0-5 scoring and social functional scale which consist of 5 questions with a 1-6 scoring.
|
4 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
House Brackmann Facial Grading Scale
Time Frame: 4 months
|
It classifies facial nerve function into six grades, ranging from Grade 1(normal function) to Grade 6 (complete paralysis).
It is widely used for assessing facial nerve recovery.
|
4 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Rimza Safdar, DPT, Elite College of Management Sciences
Publications and helpful links
Helpful Links
- In 2025, Islam Hussain and M Samir conducted a systemic review and meta analysis in which He concluded the effectiveness of mime therapy in improving clinical and functional outcomes.
- In 2019, A.F. D'Souza, S.R. Rebello conducted a study in order to compare the effectiveness of mime therapy with neuromuscular in patients with acute Bell's Palsy.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-GCUF-079255
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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