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There are many studies in the literature that study the sensory profile of children with autism spectrum disorder (ASD), which can essentially have three types of behavior: (1) Registration, (2) Seeking, (3) Sensitivity, and (4) Avoiding. However, there are few studies dedicated to the study of the sensory profile of children with autism. A child's sensory profile is closely related to the way they deal with the world and their social interaction. The existence of tools that allow the study of the behavioral response to the sounds of children with autism spectrum disorder, will allow the application of targeted therapies in the future. Therapies targeted and adjusted to each profile observed in these children will allow to attenuate these maladjusted behavioral responses, or even overcome these deficits, if there is an early and precise intervention.
Full description
The objectives of this work are:
PRIMARY OBJECTIVES:
To characterize the BAEP findings in children with ASD (case group) and compare these findings with those obtained in children matched by sex and age without suspected ASD (control group), with a special focus on the study of the following parameters:
Wave I amplitude and wave V/wave I amplitude ratio (V/I ratio)
Extension of the absolute latency of wave V
With the aim of:
Characterize the Behavioral Response to Sounds of children with ASD
To establish, among children with ASD, a relationship between the specific findings in the BAEP and different behavioral responses to sound.
SECONDARY OBJECTIVES:
MATERIAL AND METHODS
Study design: Analytical observational case-control study
Participants This study will include children between 3 and 6 years of age, observed consecutively at the Otorhinolaryngology Service of the Porto University Hospital Center and the Pediatrics Service of the Northern Mother and Child Center (belonging to the Porto University Hospital Center), with a diagnosis of ASD. with indication for performing BAEP.
Study groups
The sample will be divided into two groups:
Recruitment
All children sent/followed at the Development Consultation - Pediatrics, Pedopsychiatry or Pediatric Neurology diagnosed with ASD aged between 2 and 6 years (potential cases) and all children aged between 2 and 6 years who have BAEP appointments in the Otorhinolaryngology department (potential controls) will be sent to the principal investigator.
Thus, a consecutive and progressive recruitment of participants will be carried out. Parents or guardians of children who meet the inclusion criteria will be asked about their availability and interest in participating in the study, explaining the purpose of the study. An Information Leaflet for Participants has been created.
If they wanted to participate in the study after being duly informed, an Informed Consent Term is delivered and signed.
An individual data collection sheet was also created for data collection by the researcher. Data obtained from the electronic clinical file and provided by the parents.
The aforementioned and scheduled BAEP questionnaires will be applied.
After performing the BAEP, a new consultation is scheduled with the parents/legal guardians, where the result of the new assessment in terms of sensory and auditory profile, as well as the results of the BAEP will be made known.
All data collected will go into a database created for this purpose.
Time line
This study will be developed in 4 main stages:
st PHASE: Preparation phase
nd PHASE: Selection of possible study patients and data collection
rd PHASE: Creation of a database
th PHASE: Data analysis and interpretation of results (2 months) The researchers and statistical analysts, using the appropriate statistical tests, will proceed to the analysis of the collected data. Subsequently, an interpretation will be made of the results of the study and a comparison with existing data in the literature in order to draw up the conclusions of the study and its dissemination in Research Article format and its presentation in free communication format at scientific events. .
Ethical considerations
During the realization of this study, we will act according to the medical ethics requirements defined in the World Medical Association Declaration of Helsinki - Ethical Principles for Medical Research Involving Human Subjects. Thus, this project was submitted to the Ethics Committee for Health of the Porto University Hospital Center, obtaining a favorable opinion in May/2022 (2021-124 (101-DEFI/104-CE)).
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Exclusion criteria
120 participants in 2 patient groups
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Central trial contact
Joana Costa, MD
Data sourced from clinicaltrials.gov
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