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New treatment option for Attention Deficit Hyperactivity Disorder (ADHD)
Official title Effects of Probiotics on the Gut-brain Axis in Children
ClinicalTrials.gov ID: NCT07459699
What this study is testing
- What it's testing
- The effect of probiotics on the gut-brain axis in children with attention deficit hyperactivity disorder will be studied.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 8 to 11
You may be able to join if
- Males and females aged 8 - 11 years
- With mild ADHD symptoms
- Patient and parents (legal representatives) able and willing to participate in the research by complying with the protocol procedures
You likely can't join if
- Metabolic disorder
- Severe chronic disease
- GI disorders found to be inconsistent with the conduct of the study by the investigator
- Neurological disorder involving central function (e.g., intellectual disability, autism spectrum disorder, epilepsy, narcolepsy)
- Currently treated with a medication with primary central nervous system activity or major psychiatric condition requiring hospitalization
- With a known or suspected food allergy or intolerance or hypersensitivity to any of the study products' ingredients
See the full eligibility criteria
- Males and females aged 8 - 11 years
- With mild ADHD symptoms
- Patient and parents (legal representatives) able and willing to participate in the research by complying with the protocol procedures
- Metabolic disorder
- Severe chronic disease
- GI disorders found to be inconsistent with the conduct of the study by the investigator
- Neurological disorder involving central function (e.g., intellectual disability, autism spectrum disorder, epilepsy, narcolepsy)
- Currently treated with a medication with primary central nervous system activity or major psychiatric condition requiring hospitalization
- With a known or suspected food allergy or intolerance or hypersensitivity to any of the study products' ingredients
- Having taken prebiotic or probiotic treatment in the month prior to inclusion, or having taken antibiotics for more than one week in the 3 months prior to inclusion,
- Taking part in another clinical trial or being in the exclusion period of a previous clinical trial,
- Parents (legal representatives) presenting a psychological or linguistic incapability to sign the ICF,
- Parents (legal representatives) impossible to contact in case of emergency.
The study team makes the final eligibility decision.
Where it's taking place
- Shanghai, China
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 8 years to 11 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Shanghai, China. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.