Actively Recruiting
Effect of Neuromuscular Electrical Stimulation on Unilateral Central Facial Palsy
Led by University of Aarhus · Updated on 2026-03-09
130
Participants Needed
1
Research Sites
250 weeks
Total Duration
On this page
Sponsors
U
University of Aarhus
Lead Sponsor
D
Danish Association of Occupational Therapist
Collaborating Sponsor
AI-Summary
What this Trial Is About
Background Central facial palsy (CFP) is a common condition in stroke, with an estimated prevalence of 45%. CFP can lead to facial asymmetry, problems with mouth closure and food processing, bite marks on the cheek, social isolation, and reduced quality of life. CFP is seen as an important area of rehabilitation, and training is therefore often carried out to reduce the consequences of CFP. In a recent systematic review conducted by the principal investigator, the results showed that very few studies have been conducted that have investigated the effect of training for CFP, and there is currently no scientific evidence to support the effect of the various training interventions. Objective To investigate the effect of Neuromuscular electrical stimulation (NMES) on facial symmetry compared to usual practice, in participants with CFP as a result of stroke. Hypothesis: Participants who receive training with NMES together with usual training for facial paralysis have greater improvement in facial symmetry than participants who only receive usual training for facial paralysis. Trial design Randomized controlled trial (RCT) with a nested pilot trial. A pilot trial/RCT will be conducted in order to power calculation in an RCT. The protocol for the pilot trial and RCT will be the same, and participants from the pilot trial and their outcome data are thus expected to be included in the RCT.
CONDITIONS
Official Title
Effect of Neuromuscular Electrical Stimulation on Unilateral Central Facial Palsy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Central facial palsy
- First time stroke
- 18 years or older
- Able to provide written consent
You will not qualify if you...
- Unable to cooperate with mimical exercises
- Contraindications for neuromuscular electrical stimulation
- Admitted for a three-week assessment stay at the hospital
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hammel neurorehabilitation centre and university research clinic
Hammel, Denmark, 8450
Actively Recruiting
Research Team
J
Jesper Fabricius, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here