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Kabat Rehabilitation Versus Kinesiology Taping in Bell's Palsy

Effects of Kabat Rehabilitation Versus Kinesiology Taping Combined With Conventional Therapy on Facial Asymmetry and Functional Disability in Patients With Unilateral Bell's Palsy: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07436624
Enrollment
38
Registered
2026-02-27
Start date
2025-12-11
Completion date
2026-04-12
Last updated
2026-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bell's Palsy, Facial Paralysis

Keywords

Kabat Rehabilitation, Proprioceptive Neuromuscular Facilitation, Kinesiology Taping, Facial Asymmetry, Sunnybrook Facial Grading System, Facial Disability Index, House-Brackmann Scale, Physiotherapy

Brief summary

This randomized controlled trial aims to compare the effects of Kabat rehabilitation versus kinesiology taping, both combined with conventional therapy, on facial asymmetry and functional disability in patients with unilateral Bell's palsy. A total of 38 participants will be recruited from the University of Lahore Teaching Hospital. Participants will be randomly assigned into two groups using a lottery method. Outcomes will be assessed using the Sunnybrook Facial Grading System and the Facial Disability Index at baseline, 4 weeks, and 8 weeks.

Detailed description

This single-blinded randomized clinical trial will be conducted at the University of Lahore Teaching Hospital, Lahore. Participants aged 30-50 years diagnosed with unilateral Bell's palsy will be recruited using purposive sampling. After obtaining informed consent, 38 eligible participants will be randomly allocated into two parallel groups using the lottery method. Group A will receive conventional therapy (facial massage and electrical muscle stimulation) combined with Kabat rehabilitation using proprioceptive neuromuscular facilitation (PNF) techniques. Group B will receive conventional therapy combined with kinesiology taping applied according to a standardized protocol targeting affected facial muscles. Treatment will be administered for 8 weeks, 5 sessions per week, with each session lasting approximately 40 minutes. Assessments will be conducted at baseline, at 4 weeks, and at 8 weeks. Data will be analyzed using SPSS version 27.0.

Interventions

OTHERConventional Facial Therapy

Conventional therapy will consist of facial massage and electrical muscle stimulation (EMS). Massage techniques will include light stroking, tapping, and kneading of affected facial muscles for approximately 5 minutes. Electrical muscle stimulation will be delivered using interrupted galvanic current with a pulse width of 150 μs, frequency of 1-10 Hz, and intensity of 2-5 mA for 15 minutes. Small surface electrodes will be placed on key facial muscles including frontalis, zygomaticus major, orbicularis oris, and mentalis. Total duration of conventional therapy will be approximately 20 minutes per session.

OTHERKabat Rehabilitation

Kabat rehabilitation will be administered using proprioceptive neuromuscular facilitation (PNF) techniques. Manual resistance will be applied to stimulate contraction of affected facial muscles through three fulcrum points (upper, intermediate, and lower). Each muscle group (frontalis, corrugator supercilii, orbicularis oculi, procerus, orbicularis oris, and mentalis) will perform 10 repetitions for 2 sets. The Kabat component will last approximately 20 minutes per session. Treatment will be provided 5 sessions per week for 8 weeks.

Sponsors

University of Lahore
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

Age between 30-50 years Both genders Unilateral Bell's palsy House-Brackmann grade greater than 3 Sufficient physical and mental ability to follow instructions

Exclusion criteria

Facial skin lesions or contraindications for procedures Cranial or facial trauma within past 3 months Prior episodes of facial paralysis Craniofacial deformities or degenerative diseases Head and neck malignancy Active infection History of upper motor neuron lesion

Design outcomes

Primary

MeasureTime frameDescription
Facial Asymmetry (Sunnybrook Facial Grading System)Baseline, 4 weeks, and 8 weeksScores range from 0 to 100, where higher scores indicate better facial symmetry.

Secondary

MeasureTime frameDescription
Functional Disability (Facial Disability Index - FDI)Baseline, 4 weeks, and 8 weeksAssesses physical and social well-being related to facial function. Higher scores indicate better function.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026