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

The objective of this study is to evaluate the effectiveness of mime therapy and conventional therapy for improving facial functional mobility and coordination.

Study Overview

Detailed Description

This will be a Randomized Controlled Trial (RCT). Sample will be taken using Non-Probability Convenient Sampling. Sample size of 34 participants that will be randomly allocated into two groups using a coin toss method. Group A (intervention group) will receive mime therapy along with conventional therapy, while Group B (control group) will receive only conventional therapy were given 45 minutes per day for 3-4 sessions in a week for 3 weeks. Outcomes will be measured by using the Sunnybrook Facial Grading System for checking facial symmetry and the House-Brackmann Facial Grading System for measuring severity of paresis.

Study Type

Interventional

Enrollment (Actual)

34

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
      • Gujranwala, Punjab, Pakistan, 52250
        • Al Raee Hospital

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

  • Adult

Accepts Healthy Volunteers

No

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

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: 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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Rimza Safdar, DPT, Elite College of Management Sciences

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.

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)

April 1, 2025

Primary Completion (Actual)

June 1, 2025

Study Completion (Actual)

July 1, 2025

Study Registration Dates

First Submitted

May 30, 2025

First Submitted That Met QC Criteria

July 5, 2025

First Posted (Actual)

July 10, 2025

Study Record Updates

Last Update Posted (Actual)

July 10, 2025

Last Update Submitted That Met QC Criteria

July 5, 2025

Last Verified

July 1, 2025

More Information

Terms related to this study

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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