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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05848336
Other study ID # UskudarUGFCFAUTISM
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 26, 2020
Est. completion date January 18, 2023

Study information

Verified date May 2023
Source Uskudar University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To evaluate the efficacy of eight weeks of GFCF in children with ASD on autistic symptoms and ophthalmic findings such as corneal reflex, interpupillary distance (IPD) and pupil size.


Description:

Autism spectrum disorder (ASD) is a common condition. ASD is a heritable illness characterized by early-onset differences in interaction, communication, sensory atypicality, and stereotyped behaviors. Recent studies suggest a link between elimination diets and severity of autistic behaviors. The etiology of ASD has been still uncertain. Therefore, elucidating the underlying pathology may assist in risk assessment and facilitate process management. Non-harmful and existing evidence for the diet's benefits in ASD must be elucidated. Primary Study Objective: To assess the effect of a GFCF diet on variables autism index, stereotyped behaviors, communication, social interaction associated with ASD. The pupillary response can be utilized to anticipate neurological and physiological activities under the surface. Changes in light trigger the pupil response, which adjusts the amount of brightness falling on the retina by instinctively constricting or dilating the pupil. Atypical pupil size has been linked to abnormal autonomic function in people with ASD. Disturbances in autonomic functions may also lead to differences in the corneal reflex. This study aimed to obtain more data on the behavioral symptoms and ophthalmic measurements of gluten-free casein-free (GFCF) on ASD. In addition, normal development children and children with autism may differ in facial morphology. This study also evaluates the effect of GFCF diet on IPD distance. Secondary Objectives: To assess the role of GFCF diet in the manifestation of opthalmic measurements such as pupil size, corneal reflex and IPD. 30 children with ASD were enrolled in a 8-weeks prospective GFCF diet treatment study. In the study, a single group was evaluated with measurements before and after dietary intervention.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date January 18, 2023
Est. primary completion date March 14, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 2 Years to 11 Years
Eligibility Inclusion Criteria: - Informed consent / Assent, as applicable must be signed prior to executing any study related procedure - Children, male or female, 2 to 11 years old (inclusive) - Confirmed diagnosis of ASD according to the DSM-IV Symptom Checklist - Ability to maintain a gluten- and casein-free diet during the study Exclusion Criteria: - Cardiovascular, psychiatric, autoimmune, cancer, etc. children with secondary different disease - Children with any drug use - Children currently receiving treatment with any alternative medical methods (eg.hyperbaric). - Children with a diagnosis of celiac disease - Children who have received any dietary treatment before

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Gluten Free Casein Free Diet
Thirty children with autism were evaluated before the diet (Pre-Test) and after 8 weeks of dietary intervention (Post-Test).

Locations

Country Name City State
Turkey Üsküdar University Istanbul

Sponsors (1)

Lead Sponsor Collaborator
Uskudar University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Gilliam Autism Rating Scale 2 (GARS-2) Based on DSM-IV autism diagnostic criteria, GARS-2 is a behavior checklist for children and teenagers aged 3 to 22. The three subscales of the scale are communication, social interaction, and stereotypical behavior. Each subscale contains 14 items that are scored on a four-point scale (0: Never observed, 1: Rarely observed, 2: Sometimes observed, 3: Often observed). The total score obtained from the scale is converted into standard scores, and an OBI score is obtained. An OBI score of 85 and above indicates a high probability of having ASD, a score between 70-84 indicates a medium probability, and a score of 69 and below indicates a low probability. 8 weeks
Primary Weight (kg) Body weight was measured in kilograms. 8 weeks
Primary Body mass index Body mass index (BMI)=weight/(height)^2 8 weeks
Secondary The pupil measurements The measurements of both groups were taken from a distance of 1 meter with a binocular photo refractometer under the same conditions, without cycloplegia. Plusoptix® A09 an measure a pupil size of 4.0-8.0 mm in 0.1 mm steps. Eccentric photorefraction is used as a measurement basis. The device provides convenience in terms of pediatric evaluation with its remarkable features. The pupil measurements were performed by an ophthalmologist in the outpatient clinical unit. The brightness level in the room was controlled via the lux meter application. Pupil size (mm) was measured at least three times after each participant was left in a room with a light level of 8 cd/m2 for 2 minutes. The average value of 3 consecutive consistent measurements was recorded. 8 weeks
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