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Nutritional Intervention for Children With ASD and/or ADHD

Nutritional Intervention in Children With ASD and/or ADHD: Randomized Controlled Trial With Probiotics.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05167110
Acronym
PRONED
Enrollment
80
Registered
2021-12-22
Start date
2020-02-03
Completion date
2022-03-31
Last updated
2024-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ADHD, ASD, Microbiota, Probiotics

Brief summary

Based on alterations in the intestinal microbiota in children with ASD and the high comorbidity between ASD and ADHD, the aim of this project was to assess whether the administration of probiotics with strains related to the production of the neurotransmitters dopamine and GABA had a positive effect on social behavior, attention, and behavior.

Detailed description

We hypothesized to find differences in the composition and / or function of the microbiota of the gastrointestinal tract of children with ASD and / or ADHD. We consider that the intervention with probiotics (and specifically with GABA and dopamine producing strains), can modify the composition and / or function of the GIT microbiota and change the child's behavior, partially reducing the symptoms of attention deficit, anxiety, irritability, impulsivity and restlessness associated with diagnoses and consequently, we believe that it could improve the quality of life for children and their families. Apart from the clinical evaluation of the disorder and associated psychopathological symptoms and neuropsychological deficit, the diet, lifestyle and anthropometric characteristics of the child will be evaluated, which can influence the composition and / or function of gut the microbiota. The sample that will be part of the study will be 80 children, 40 with a diagnosis of ASD and 40 with a diagnosis of ADHD. These children will randomly receive placebo or probiotic intervention for 12 weeks.

Interventions

DIETARY_SUPPLEMENTPlacebo

Children assigned to the groups (ASD/ADHD) will be randomly prescribed placebo supplementation for 12 weeks (placebo subgroup).

DIETARY_SUPPLEMENTProbiotic

Children assigned to the groups (ASD/ADHD) will be randomly prescribed supplementation with two GABA- and dopamine-producing strains at a total of 1 x 10 (9) CFU/capsule for 12 weeks (probiotic subgroup).

Sponsors

University Rovira i Virgili
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

ABBiotics has been the producer of probiotics and who knows the masking

Eligibility

Sex/Gender
ALL
Age
4 Years to 16 Years
Healthy volunteers
Yes

Inclusion criteria

* Parental informed consent, * ASD and ADHD will meet the DSM diagnoses (edition IV-TR or 5) criteria * Ages between 5 and 16 years * To complete period (12weeks) of taking the probiotic

Exclusion criteria

* Having suffered adverse effects in the previous administration of probiotics * Being on probiotics 3 months before the start of the intervention * To suffer any medical illness incompatible with the administration of probiotics * Having intolerances or allergies to the excipient of the treatment (probiotic or placebo) * Taking antibiotics in the start of the intervention.

Design outcomes

Primary

MeasureTime frameDescription
Continuous Performance Test (CPT 3 or CPT-K 2)12 weeksMeasures attention and inhibitory control
Social Responsiveness Scale™, Second Edition12 weeksAssess severity of the ASD manifestations answered by parents
Conners scale12 weeksAssess severity ADHD symptoms answered by parents
Behavior Rating Inventory of Executive Function (BRIEF-2)12 weeksAssess severity ADHD symptoms answered by parents

Secondary

MeasureTime frameDescription
Gastrointestinal symptoms12 weeksDiscomfort/abdominal lower pain
Child Behavior Checklist (CBCL)12 weeksemotional and behavioral symptoms
Physical Activity (PAQ-C)12 weeks

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026