Kabat Rehabilitation Versus Mime Therapy on Facial Disability and Synkinesis in Patients of Bell's Palsy

Sponsor
University of Lahore (Other)
Overall Status
Recruiting
CT.gov ID
NCT06029855
Collaborator
(none)
85
1
2
5.5
15.5

Study Details

Study Description

Brief Summary

Bell's palsy, also called idiopathic facial paralysis, is a common cause of unilateral facial paralysis. It is one of the most common neurological disorders of the cranial nerves.

Condition or Disease Intervention/Treatment Phase
  • Other: Kabat Therapy
  • Other: Mime Therapy
N/A

Detailed Description

Bell's palsy is an alarming condition of rapid onset, which paralyzes half of the facial muscles. Kabat rehabilitation is a manual resistance technique that promotes a basic pattern of movement through facilitation, inhibition, and resistance of a group of muscles. It increases the functioning and power of facial muscles while Mime therapy results in immediate improvement of function and integrity of facial muscles. It also mitigates synkinesis in Bell's palsy. Both techniques are easy to apply. They are clinically important techniques that are easily understood by patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
85 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects Of Kabat Rehabilitation Versus Mime Therapy On Facial Disability And Synkinesis In Patients Of Bell's Palsy
Actual Study Start Date :
May 1, 2023
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Oct 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Kabat Therapy

Kabat exercises primarily assist functional response in defective muscles through the general structure of muscles experiencing resistance. After 6th week, resting and voluntary symmetries were recorded.

Other: Kabat Therapy
The participants of group A will receive Kabat Rehabilitation with routine physical therapy. The protocol will be given to the participants for three sessions/week for six weeks. Each session will be of 30 minutes.

Experimental: Mime Therapy

Mime therapy utilizes emotional input to access better movement patterns. It is beneficial as it improves circulation and maintains muscle properties.

Other: Mime Therapy
The participants of group B will receive Mime Therapy in addition to routine physical therapy. The protocol will be given to the participants once a week for six weeks, while physical therapy will be given on alternate days. Each session will be of 30 minutes.

Outcome Measures

Primary Outcome Measures

  1. Change in Synkinesis [It will be assessed at baseline, at the third week and at six week.]

    Synkinesis will be accessed through the "House-Brackmann Scale". It is classified as a universal scale. This scale analyses the symmetry, synkinesis, stiffness, and global mobility of the face. It is divided into six categories (normal, mild dysfunction, moderate dysfunction, moderately severe dysfunction, severe dysfunction, and total paralysis) and is a 0-6-point scale with 6 representing total paralysis.

  2. Level of Facial Disability [Change in functional status will be measured at the baseline, at 3rd week and at 6th week.]

    The level of Facial disability will be measured through the "Facial Disability Index Scale". This scale has ten items that evaluate the patient's physical and social aspects (mastication, deglutition, communication, labial mobility, emotional alterations, and social integration). It uses a hundred-point scale with a higher score indicating less impairment. 24 Minimum score for physical functioning: 0, Maximum score for physical functioning: 25, Minimum score for social and well-being: 5, Maximum score for social and well-being.

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age group 25-50 years.

  2. Both male and female.

  3. Unilateral bell's paralysis.

  4. Not congenital in origin.

  5. Sub-acute and chronic cases.

Exclusion Criteria:
  1. Other neurological deficits include epilepsy and Alzheimer's disease.

  2. Traumatic onset.

  3. Surgical reconstruction (nerve or muscle reconstruction).

  4. Mental and psychological disorders i.e., schizophrenia, bipolar disorders.

  5. Skin diseases (eczema, urticarial) as electrical stimulation may affect the results.

  6. Any contraindications for massage like sunburn, bruising, or cuts.

Contacts and Locations

Locations

Site City State Country Postal Code
1 The University of Lahore Lahore Punjab Pakistan 5400

Sponsors and Collaborators

  • University of Lahore

Investigators

  • Study Chair: Ashfaq Dr Ahmed, PhD, The University of Lahore

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Lahore
ClinicalTrials.gov Identifier:
NCT06029855
Other Study ID Numbers:
  • REC-UOL-406-05-2023
First Posted:
Sep 8, 2023
Last Update Posted:
Sep 13, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of Lahore
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 13, 2023