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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05614206
Other study ID # 897
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 26, 2022
Est. completion date September 26, 2024

Study information

Verified date November 2022
Source IRCCS Eugenio Medea
Contact Valentina Riva, PhD
Phone +39031877924
Email valentina.riva@lanostrafamiglia.it
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This project deals with essential challenges in the context of Autism Spectrum Disorder benefiting from a prospective design in childhood, early intervention and a cutting-edge experimental techniques. The present study tests the potential effect of early intervention on neural and behavioral responses in toddlers at elevated likelihood of developing autism (siblings of children with autism) who show clinical autistic signs. Four comparison groups were included in the study: (1) toddlers at elevated likelihood of developing autism with clinical autistic signs who receive early intervention from 18 to 24 months (2) toddlers at elevated likelihood of developing autism with clinical autistic signs who do not receive early intervention (3) toddlers at elevated likelihood of developing autism without clinical autistic signs who only received assessment and monitoring, and (4) typically developing toddlers who only received assessment and monitoring. This study focuses on social and nonsocial sensory integration skills (measured by electroencephalographic and eyetracking recordings) to identify reliable biomarkers for early detection and intervention of autism during a critical period of development. The characterization of biomarkers will guide the detection of the most vulnerable children that will benefit from early intervention, with the long-term aim of reducing the impact of autism on the National Health System.


Recruitment information / eligibility

Status Recruiting
Enrollment 80
Est. completion date September 26, 2024
Est. primary completion date September 26, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Months to 24 Months
Eligibility Inclusion Criteria: - Toddlers aged between 18 and 24 months - Toddlers at elevated likelihood of developing autism, because siblings of children with a diagnosis of autism (for group 1, 2, and 3) Exclusion Criteria: - Gestational age <36 weeks and/or birthweight < 2000 grams - Griffiths general quotient at 18 months < 70 - presence of major complications in pregnancy and/or delivery likely to affect brain development - presence of neurological deficits, dysmorphic markers, or other medical conditions.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavioral intervention based on Applied Behavior Analysis principles
Intervention sessions are conducted by licensed therapists with a training in applied behavior analysis or behavior analysts. One-to-one interventions for 3 h/week are carried out over a period of 5 months. The intervention focused on two target symptoms, imitation and joint attention, as two of the pivotal skills in early development. Behavior analytic techniques are used, including discrete trial, shaping for positive reinforcement, systematic prompting and fading procedures, and reinforcement procedures, according to the published manual. Imitation sessions start with imitation recognition and imitation of familiar actions (gestural and object imitation) and end with the imitation of novel actions. Joint attention evolvs from initiating requests (starting with gaze shift with the child looking away from an interesting object to the adult and back) to coordination of gaze shift, vocalization and gestures through reaching, and pointing and showing behaviors.

Locations

Country Name City State
Italy Associazione La Nostra Famiglia - IRCCS Eugenio Medea Bosisio Parini Lecco

Sponsors (1)

Lead Sponsor Collaborator
IRCCS Eugenio Medea

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of electroencephalographic theta power (theta frequency band) Electroencephalographic theta power to synchronous/asynchronous social and nonsocial stimuli will be measured as an index of social and sensory processing in the 4 groups at T0 (18 months) and T1 (24 months). High-density 128 channel is recorded continuously throughout the session once at 18 months of age
Primary Change of electroencephalographic theta power (theta frequency band) Electroencephalographic theta power to synchronous/asynchronous social and nonsocial stimuli will be measured as an index of social and sensory processing in the 4 groups at T0 (18 months) and T1 (24 months). High-density 128 channel is recorded continuously throughout the session once at 24 months of age
Primary Change of looking behavior (time of fixations to Area of Interests) and pupillometry parameters (pupil diameter) Time of fixations (milliseconds) in different Areas of Interests (i.e., month and eyes) and pupil diameters (millimeters) will be recorded and analysed in the 4 groups at T0 (18 months) and T1 (24 months) once at 18 months of age
Primary Change of looking behavior (time of fixations to Area of Interests) and pupillometry parameters (pupil diameter) Time of fixations (milliseconds) in different Areas of Interests (i.e., month and eyes) and pupil diameters (millimeters) will be recorded and analysed in the 4 groups at T0 (18 months) and T1 (24 months) once at 24 months of age
Secondary Change of standardized scores of clinical measures Standardized scores (i.e., z-scores, T-scores) of clinical tests (Griffiths Scales, Autism Diagnostic Observation Schedule-Second Edition, McArthur Questionnaire Sensory Profile) will be measured and will be correlated with electroencephalographic (theta power) and eyetracking (looking behavior and pupillometry parameters) data Twice: at 18 and at 24 months of age
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