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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06340009
Other study ID # REC/01743
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 22, 2024
Est. completion date August 25, 2024

Study information

Verified date March 2024
Source Riphah International University
Contact Mulazam Imran, MS-NMPT*
Phone 03236791525
Email mulazimimran04@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Bell's palsy, characterized by unilateral paralysis/paresis of facial muscles, is a condition with a significant impact on individuals' lives. It was first identified by scientist Sir Charles Bell, and its sudden onset can lead to social, psychological, and emotional distress. Left untreated, Bell's palsy can have long-lasting effects on a patient's quality of life, including loss of facial muscle control, emotional stress, and communication difficulties. Rehabilitation protocols encompass various physical therapy techniques, among which Mime therapy and Motor imagery technique have shown promise.


Description:

While rehabilitation protocols have shown promise in enhancing facial muscle control, reducing disability, and preventing long-term complications, there remains a critical gap in the literature regarding the comparative effectiveness of various rehabilitation techniques. Currently, there is limited empirical evidence to guide healthcare professionals in selecting the most suitable rehabilitation approach for individual patients. The purpose of this study is to address this gap in knowledge by comparing two specific rehabilitation techniques: Mime therapy and Motor imagery technique. Understanding which of these rehabilitation techniques is more effective can significantly influence clinical practice and patient care. By conducting a systematic comparison, this study aims to provide evidence-based recommendations to healthcare professionals in selection of appropriate rehabilitation protocol for Bell's palsy patients.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date August 25, 2024
Est. primary completion date August 22, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - Age 20-40 years - Both male and female - Patients diagnosed with Bell's Palsy - Paralysis/paresis of all muscle groups of one side of face Exclusion Criteria: - Patients diagnosed with facial palsy - Patients with impaired cognition - Patients diagnosed with other neurological diseases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
mime therapy
Facial Massage Frowning Close eyes Smile Fish Face Eyebrow raising Breathing exercise Blow cheeks Mouth opening and closing. Moving lips side to side Blow a candle. Nasal flaring Chewing exercise Rinse mouth Speaking vowels Fill mouth with water Fill rubber balloon Sucking water with straw
motor imagery
Raising your eyebrows Showing angry face Closing and opening eyes Pouting Blowing cheeks Smiling Nasal flaring Blowing candle Deviating lips side to side Chewing something Speaking vowels

Locations

Country Name City State
Pakistan Muzaffar Hospital Sargodha

Sponsors (1)

Lead Sponsor Collaborator
Riphah International University

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary House-Brackmann Scale (HBS) A widely used scale to assess facial nerve dysfunction.Grades facial muscle function from I (normal) to VI (total paralysis). - Higher scores indicate more severe dysfunction. week 6
Primary Facial Disability Index (FDI) A patient-reported outcome measure assessing the impact of facial palsy on daily life.Assesses physical, social, and emotional functioning - Uses a questionnaire. - Higher scores indicate a greater impact on daily life. week 6
Primary Sunnybrook Facial Grading System An assessment tool for evaluating facial muscle function, including static and dynamic aspects. week 6
Primary Synkinesis Assessment Questionnaire (SAQ) An assessment tool specifically designed to evaluate synkinesis- related symptoms. Assesses the presence and severity of synkinesis symptoms during voluntary actions. - Uses a questionnaire. - Higher scores indicate more severe synkinesis-related symptoms. week 6
See also
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