Effect of Masticatory Electrical Stimulation on Dysphagia in Spastic Cerebral Palsy
NCT ID: NCT04086355
Last Updated: 2019-09-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
40 participants
INTERVENTIONAL
2017-08-01
2019-02-11
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Feasibility Of Oral Sensorimotor Stimulation On Oropharyngeal Dysphagia In Children With Spastic Cerebral Palsy
NCT04524559
Effect of Kinesio Tape on Oral and Pharangeal Swallowing Phases in Children With Spastic Cerebral Palsy
NCT06157489
Effect of Trunk Stabilization Exercises on Quality of Life and Communication in Cerebral Palsy
NCT04214080
The Effects of Oral Facial Facilitation and Oral Motor Therapy in Dysphagia
NCT06785220
EFFECT OF NEUROMUSCULAR ELECTRICAL STIMULATION ON DYSPHAGIA IN CHILDREN WITH DOWN SYNDROME
NCT05277142
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
A randomized controlled clinical trial was conducted after interviews were done with the parents or care givers of all children, before starting the study to demonstrate the aim, procedures and potential benefits of the study. Children' parents provided written informed consent before the study was conducted.
Participants:
Forty spastic CP children (26 girls and 14 boys), age ranging from 2 to 5 years, participated in this study. They were selected based on the following criteria; having at least score (level 4) according to functional oral intake scale (FOIS), and they had good head control. Children were excluded if they had; oral hypersensitivity, acute or chronic dental problems, released primitive reflexes as asymmetrical tonic neck reflex or Seizures.
Participants who met the eligible criteria were assigned randomly to either study or control group of equal numbers. Each child in both groups received an oro-motor exercises program as home routine 3 times daily before each meal. Children in the study group received 20-minutes of neuromuscular electrical stimulation (NMES) (multi current SND 64227) which consisted of two-channels electrotherapy system designed for neuromuscular rehabilitation. The NMES was applied with 60 Hz of 230 milliseconds twice weekly for 8 weeks. While participants in the control group received placebo NMES.
Procedures:
Assessment:
1. weight and height Weight and height of each child were measured pre and post treatment by using weight and height measuring scale.
2. Feeding level Dysphagia feeding level was assessed by using functional oral intake scale (FOIS) , taking into consideration that tube dependent children at levels from 1-3 were excluded from the study).
3. Assessment of oromotor skills by oromotor assessment scale (OMAS).
Treatment:
Home routine exercises The exercises were demonstrated to the parents to warrant the uniformity of the training program. They were instructed to conduct the exercises three times daily before each meal. This home routine included passive movement, active movement and sensory stimulation.
1. Passive movement exercises:
Passive movement included massage and passive range of motion (ROM) exercises. A-Massage: for gums, cheeks, lips and tongue for ten repetitions.
* Gum massage: upper and lower gum massage started from middle of the gum to the end in the right and left side using regular brush.
* Lip massage: started from side to side, it was applied for the upper then the lower lips.
* Cheek massage: Applied intra oral in a circular way.
* Tongue massage: Applied in the lateral side of the tongue from backward to forward direction in the right and left side using regular tooth brush.
B-Passive range of motion was done for jaw, tongue and lips for ten repetitions.
* Jaw movement: cupping lower jaw and move it up and down.
* Tongue movement: Moving tongue laterally (right and left) and upward directions were done by tongue depressor and fingers.
* Movement for lip closure: pushing the lips passively against each other like a kissing position.
2. Active movements:
Active movement included active ROM for jaw, cheeks and lips and stretching for lips.
A-Active ROM
* Active jaw ROM: Jaw closure against resistance through biting on tongue depressor and holding for 6 seconds with ten times repetition.
* Active cheek ROM: Cheek compress by drinking from straws with different diameters.
B- lip stretching; Stretching upper and lower lips sustain twenty seconds for three sets.
3. Sensory stimulation; Sensory stimulation was done through Lollipop exercise by stimulation of lip closure, cheek and tongue movement through moving the lollipop in different directions.
Neuromuscular electrical stimulation The NMES was applied by the neo-faradic stimulation (Two channels system. The electrodes were applied bilaterally. The first channel was applied over the neck between the hyoid and jaw, (approximately on the belly of the digastric muscle). The second channel was applied on the side of the face, (approximately on the masseter muscle). The intensity level was determined by visible muscle contractions without pain sensation. For children in the study group, the intensity level was from 7 mA to 15 mA, the time of rise and fall was equal (50% raise and 50% fall) and the time on and off was fixed as; 3,1s:3,1s. While those in the control group received placebo NMES without any signals reached to the muscles.
All children received the treatment sessions 20 minutes, twice/weekly for 2 months in addition to home routine exercises.
Statistics:
Paired and unpaired t-test were conducted for comparison of the mean and slandered deviation for the demographic characteristics, weight gain and height variables. Mann-Whitney U test was conducted for comparison of median values of FOIS between both groups. Wilcoxon Signed Ranks Test was conducted for comparison between pre and post treatment median values of FOIS in each group.
The level of significance for all statistical tests was set at p \< 0.05. All statistical measures were performed through the statistical package for social studies (SPSS) version 22 for windows.
Results:
General characteristics of participants:
The pretreatment comparison between both groups showed insignificant difference regarding the mean values of age, weight and height (p\<0.05).
Regarding weight gain and height there was insignificant difference between both groups before and after treatment (p\>0.05). While pre and post treatment within group comparison revealed significant difference in both groups (p\<0.05).
Regarding the feeding level (FOIS) comparison of values between both groups considering the feeding level showed a statistically significant difference in each group after treatment. While between both groups, there was insignificant difference before treatment (p\>0.05). After treatment, there was significant difference between the study and the control groups in FOIS (p\<0.05).
Regarding to oromotor skills There was insignificant difference between both groups before and after treatment (p\>0.05), While a significant different was in each group after treatment when comparing it with its pretreatment value was recorded (p\<0.05)
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Effect of electrical stimulation on dysphagia in cp
the study group that was treated by selected oromotor exercise program in addition to neuromuscular electrical stimulation, Feeding level progress was evaluated by functional oral intake scale,oro motor skills were evaluate by oromotor assessment scale, weight gain and height were measured pre and post 2 months of the treatment.
oromotor exercises and neuromuscular electrical stimulations
treatment study group with occupational exercises and electrical stimulation
effect of oromotor exercise on dysphagia in cp
the control group was treated by the same oromotor exercise program in addition to placebo effect of neuromuscular electrical stimulation. Feeding level progress was evaluated by functional oral intake scale,oro motor skills were evaluate by oromotor assessment scale, weight gain and height were measured pre and post 2 months of the treatment.
oromotor exercises and neuromuscular electrical stimulations
treatment study group with occupational exercises and electrical stimulation
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
oromotor exercises and neuromuscular electrical stimulations
treatment study group with occupational exercises and electrical stimulation
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* age ranged from 2 to 5 years.
* They had score level 4 or more according to functional oral intake scale (FOIS)
* They had head control
Exclusion Criteria
* any acute or chronic dental problems
* released primitive reflexes as asymmetrical tonic neck reflex.
* seizures
* genetic syndrome
2 Years
5 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Cairo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
amira farag
Principal Investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Out Patient Clinic Faculty of Physical Therapy Cairo University
Dokki, Giza Governorate, Egypt
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
P.T.REC/012/001630
Identifier Type: REGISTRY
Identifier Source: secondary_id
NCT04086355
Identifier Type: REGISTRY
Identifier Source: secondary_id
P.T.REC/012/001630
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.