Effectiveness of ES and MT VS ES and PNF Technique Among Bells Palsy Patients
Effectiveness of Electrical Stimulation and Mime Therapy Versus Electrical Stimulation and PNF Technique Among Bells Palsy Patients
1 other identifier
interventional
56
1 country
1
Brief Summary
To determine the effectiveness of electrical stimulation with MIME therapy versus electrical stimulation with PNF technique for improving strength \& restoring lost motor function in the patients of Bell's palsy
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 18, 2023
CompletedStudy Start
First participant enrolled
April 1, 2023
CompletedFirst Posted
Study publicly available on registry
May 12, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2023
CompletedMay 12, 2023
May 1, 2023
2 months
March 18, 2023
May 2, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Facial disability index(FDI) Scale
Physical function, Difficulties
6 Months
Study Arms (2)
Electrical Stimulation and Mime Therapy
OTHERElectrical Stimulation and PNF Technique
EXPERIMENTALInterventions
electrical stimulation with the MIME therapy and protocol
electrical stimulation with the PNF technique with the routine physical therapy
Eligibility Criteria
You may qualify if:
- Acute, unilateral, lower motor neuron bells palsy patient with house-backmann scale 4
- Acute onset 1-3 weeks
- Age group 20-40 years
- Who were are willing to be a part of the study
- Patients with the Bell's palsy (Facial paralysis , idiopathic facial paralysis and the herpetic facial paralysis)
You may not qualify if:
- Patient who had the autoimmune disorder, tumors, recent head injury
- The subject long with the surgery for ear and the fascial nerve palsy
- Metal dental implants, and pregnant women
- The patient with any peripheral vascular diseases
- Central fascial palsy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Superior University CRC
Lahore, Punjab Province, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 18, 2023
First Posted
May 12, 2023
Study Start
April 1, 2023
Primary Completion
June 1, 2023
Study Completion
August 31, 2023
Last Updated
May 12, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share