EEG Changes in Pediatrics With Language Dysfunction Evaluation of Sleep EEG Changes in Paediatric Patients With Language Dysfunction: A Follow up Study. EEG Changes in Pediatrics With Language Dysfunction
NCT ID: NCT05487521
Last Updated: 2022-08-04
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
PHASE3
93 participants
INTERVENTIONAL
2020-02-20
2022-05-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
In our study , Investigators evaluated the sleep EEG changes in pediatrics with languague dysfunction then in patients with EEG changes , investigators gave treatment according to type of EEG changes and investigators did a follow up assessment of language , EEG changes and frequency of clinical seizures if present at first .
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Specific Language Impairment (SLI) in Children May Caused by Epileptic Brain Activity
NCT04141332
Cognitive Impairments in Children With Epilepsy
NCT05097742
The Short-term Verbal Memory Endophenotype for Developmental Language Disorder Language Disorder
NCT06968169
Searching of Apraxia of Speech in Children With Specific Language Impairment
NCT05584033
Developmental Language Difficulties: Behavioural and Electrophysiological Studies
NCT02872870
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Electrographic status epilepticus in sleep or continuous spike - wave in slow wave during sleep, is a typical feature of acquired epileptic aphasia feature in sleep, or continuous spike-wave in slow-wave sleep, is a typical.
Our study screened for sleep potentiated epileptiform discharges in children with language dysfunction and effect of treatment of these epileptiform discharges on language dysfunction improvement.
The aim of our work :
* The primary aim of this work was to screen for sleep potentiated epileptiform discharges in children with language dysfunction.
* To evaluate effect of treatment of these epileptiform discharges on Language dysfunction improvement .
Patients and methods :
* Type of Study: Observational longitudinal study.
* Study Period: From February 2020 till November 2021 .
* Study Population: Patients was recruited from the Pediatric Neurology Clinic, Pediatric Outpatient Clinic, Phoniatrics Outpatient Clinic and the Inpatient Neurology ward at the Ain Shams University Children hospital, Cairo, Egypt.
* Inclusion Criteria: The study was conducted on Children with :
* Language delay (their language age is below their chronological age ),or Language regression (any convincing report of loss of previously acquired language skills, whether or not prior language development was reported as normal or delayed) (Meilleur et al., 2009)
* Age from 3 to 10 years old.
* Exclusion Criteria:
* Patients with hearing problems.
* Patients whose language delay can be explained by organic disease (e.g. post Hypoxic ischemic encephalopathy, known inborn error of metabolism - whether this language delay is isolated or occurring in the context of global developmental delay).
* Patients with mental delay.
* Patients with autism spectrum disorder ( according to DSM-5 standardized criteria, 2013)
* Enviromentally deprived patients.
* Sampling Method: Consecutive random sampling .
* Sample Size: 93 patients with delayed or regressed language development. (Using PASS 11 program for sample size calculation and according to Nasr et al. (2001), the expected frequency of children with epileptiform discharges =15-60%, assuming that frequency in study population =40%±10%, sample size of 93 children can detect this frequency at 95% confidence level).
* Ethical Considerations: A written informed consent was taken from the parents or legal guardians before enrolment, after fully explaining to them the nature of the study.
The approval of the Research Ethics Committee at Ain Shams University was obtained ( M.D 4312020 ) .
* Study Procedures:
1. Full history taking:
* Detailed developmental history.
* Family history of same condition.
* History of seizures.
2. Clinical examination including:
* General examination.
* Full neurological examination.
* Vocal tract examination.
3. Clinical diagnostic aids :
* IQ assessment by rapid screening test of Stanford Binet 5th version (Hanoura, 2002).
* Assessment of language age by modified pre-school language screening test - the Arabic version (Abou-Hassiba, 2011).
4. Investigations:
* MRI of the brain will be done. ((1.5 T) Phillips Achieva and Inginea )
* Auditory brainstem response (ABR). (GSI Audera will be used for acquiring ABR waveforms).
* 90 minutes sleep EEG (one full sleep cycle) (using Nicolet REF 515-019000 rev 06, CareFusion, Middletown, WI 53562, USA) and placing electrodes by 10-20 placement system.
Patients whose EEG showed epileptogenic activity ,received treatment and a follow up EEG and Assessment of language age by modified pre-school language screening test - the Arabic version will be done after 6 months.
* Statistical Analysis: Numerical data will be summarized using mean and standard deviations or medians and inter quartile ranges. Qualitative data will be presented as count and percentage, p-value \<0.005 will be considered significant.
* Statistical Package: Statistical analysis will be performed with statistical package for social science (SPSS)version 23.0 (SPSS Inc., Chicago, Illinois, USA).
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
SCREENING
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Patients without EEG changes or clinical seizures
No interventions assigned to this group
Patients with EEG changes or clinical seizures
Methylprednisolone and or prednisolone
we gave methylprednisolone and or prednisolone to patients with EEG activity and follow up the effect of the drug on language
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Methylprednisolone and or prednisolone
we gave methylprednisolone and or prednisolone to patients with EEG activity and follow up the effect of the drug on language
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Age from 3 to 10 years old.
Exclusion Criteria
* Patients whose language delay can be explained by organic disease (e.g. post Hypoxic ischemic encephalopathy, known inborn error of metabolism - whether this language delay is isolated or occurring in the context of global developmental delay).
* Patients with mental delay.
* Patients with autism spectrum disorder ( according to DSM-5 standardized criteria, 2013)
* Enviromentally deprived patients.
3 Years
10 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Ain Shams University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Omnia Alaa Mahsoub Abdelsalam
Principal investigator
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Omnia Alaa Mahsoub
Cairo, , 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.
M.D4312020
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.