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The Effect of a Multispecies Probiotics on Autism Symptoms in Children

The Effect of a Multispecies Probiotics on Autism Symptoms in Children

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06448767
Acronym
PROBAUT
Enrollment
110
Registered
2024-06-07
Start date
2024-08-07
Completion date
2026-07-30
Last updated
2026-01-08

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

Conditions

Autism Spectrum Disorder

Keywords

Autism Spectrum Disorder, Probiotics

Brief summary

In this trial, the investigators aim to evaluate the impact of a multispecies probiotic consisting of Bacillus subtilis W201, Bifidobacterium infantis W17, Bifidobacterium lactis W51, Lactobacillus acidophilus W37, Lactobacillus brevis W63, Lactobacillus rhamnosus W140, Lactococcus lactis W19, Propionibacterium freudenreichii W200, on the severity of autism symptoms, quality of life, gastrointestinal symptoms, sleep disturbances, parental stress levels and urinary p-cresol concentrations in children with Autism Spectrum Disorder aged 7 to 15 years.

Detailed description

This study is a randomized, double-blind, placebo-controlled clinical trial. One hundred and ten children aged 7 to 15 years diagnosed with Autism Spectrum Didorder will be randomly assigned in a 1:1 ratio to receive either a multispecies probiotics or a placebo for 12 weeks. The probiotic mixture contains 5 x 10\^9 colony forming units per dose consisting of Bacillus subtilis W201, Bifidobacterium infantis W17, Bifidobacterium lactis W51, Lactobacillus acidophilus W37, Lactobacillus brevis W63, Lactobacillus rhamnosus W140, Lactococcus lactis W19, Propionibacterium freudenreichii W200. The primary outcome will be the assessment of core autism symptoms using the Autism Symptom Rating Scales (ASRS). The secondary outcomes will include: the quality of life measured by the Quality of Life in Autism Part A questionnaire (QoLA-A), evaluations of sleep impairments using Children Sleep Habit Questionnaire - Abbreviated (CSHQ-A), parental stress levels using Parenting Stress Index-III (PSI-III), gastrointestinal symptoms using Gastrointestinal Symptom Rating Scale (GSRS), and urinary p-cresol levels. These outcomes will be assessed twice: at baseline and after 12 weeks of intervention.

Interventions

DIETARY_SUPPLEMENTMultispecies probiotics

Multispecies probiotics consisting of Bacillus subtilis W201, Bifidobacterium infantis W17, Bifidobacterium lactis W51, Lactobacillus acidophilus W37, Lactobacillus brevis W63, Lactobacillus rhamnosus W140, Lactococcus lactis W19, Propionibacterium freudenreichii W200 at a dose of 5x10\^9 Colony Forming Units (CFU), once daily, orally.

OTHERPlacebo

Placebo identical in taste, smell and color to the multispecies probiotics.

Sponsors

Winclove Probiotics B.V.
CollaboratorINDUSTRY
Medical University of Warsaw
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 15 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of ASD according to the Diagnostic and Statistical Manual of Mental Disorders, the fifth edition (DSM-5) or International Classification of Diseases, Tenth Revision (ICD-10). 2. Children either not taking any medication or receiving the same medication for the last 2 months. 3. Patients, or their parents/caregivers, are willing to provide written informed consent, proceed with nutritional supplements throughout the 3-month trial, refrain from starting any kind of special diet for the duration of the study, and complete the questionnaires at two time points during the study.

Exclusion criteria

1. Use of antibiotics in the previous 2 months before enrolling (excluding topical antibiotics). 2. Use of probiotics or synbiotics within the previous 2 months. 3. History of intolerance or allergy to probiotics, synbiotics or any other study product component. 4. Surgery with bowel resection or short bowel syndrome. 5. Children with severe immunodeficiency.

Design outcomes

Primary

MeasureTime frameDescription
The Autism Spectrum Rating Scales (ASRS)0-3 monthsAssessment of the severity of ASD symptoms. Scores are reported as percentiles, with higher values indicating greater symptom severity.

Secondary

MeasureTime frameDescription
The Parenting Stress Index, 4th Edition (PSI-4) / SIPA (Stress Index for Parents of Adolescents)0-3 monthsAssessment of the parenting stress intensity. The level of parental stress will be assessed using the PSI-4 questionnaire if the child is under 11 years old, or the SIPA if the child is 11 years or older. Scores range from 101 to 505 points for the PSI-4 and 90 to 450 points for the SIPA. Higher scores indicate higher level of stress.
Children Sleep Habit Questionnaire - Abbreviated (CSHQ-A)0-3 monthsAssessment of the sleep impairments. Scores range from 0 to 154 points, with higher values indicating a greater severity of sleep disturbances.
The Quality of Life in Autism Part A (QoLA-A)0-3 monthsAssessment of the quality of life of parents of children with ASD. Scores range from 28 to 140 points, with higher values reflecting a better quality of life.
Gastrointestinal Symptom Rating Scale (GSRS)0-3 monthsAssessment of the severity of gastrointestinal symptoms. Scores range from 15 to 105 points, with higher values indicating greater severity of gastrointestinal symptoms.
P-cresol levels in urine samples0-3 monthsAssessment of the level of p-cresol in urine samples.

Countries

Poland

Contacts

Primary ContactMaja Kotowska, MD
kotowska.maja@gmail.com+48223179536
Backup ContactJan Łukasik, MD, PhD
jan.lukasik@wum.edu.pl+48223179536

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026