Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06290258

Fecal Microbiota Transplantation for Patients With Autism Spectrum Disorder.

This study aims to evaluate the efficacy of fecal microbiota transplantation on the gastrointestinal symptoms, autistic symptoms and emotional behavior symptoms of patients with autism spectrum disorder, and investigate the relations between the brain-gut axis, cytokines and autism spectrum disorder. Fecal microbiota transplantation have the potentials to improve intestinal microbiota composition, regulate immunity, and then improve gastrointestinal symptoms, autistic symptoms, emotional behavior symptoms and sleep of children with autism spectrum disorder. Early intervention at school-age may even benefit development, improve cognition and prognosis.

Recruiting

Interested in participating?

Request Info

Key information

Age range

7 year–30 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

Primary location

About this study

Autism spectrum disorder (ASD) is an early neuropsychiatric developmental disorder. About 7-90% of patients with ASD have gastrointestinal problems which can relate to abnormal intestinal microbiota. The brain-gut axis can play a key role in the development of brain, and the interaction between microbiota and central nerve system can relate to the pathophysiology of ASD. Fecal Microbiota Transplantation (FMT) has just been used in the treatment of ASD in recent years. It has the potential to improve gastrointestinal, autistic, emotion and behavior symptoms of patients with ASD. Studies of its efficacy are still scarce, and no study has been conducted in Taiwan.

The purpose of this study is to treat patients with ASD by the fecal microbiota transplantation and evaluate its efficacy in gastrointestinal, autistic, emotion and behavior symptoms. It aims to prove the correlations between the brain-gut axis, intestinal microbiota, cytokines and ASD. FMT may improve and change the composition and diversity of intestinal microbiota of patients with ASD and modulate their immune reactions and subsequently improve gastrointestinal, autistic, emotion and behavior symptoms, as well as sleep. Early intervention by FMT in children with ASD may improve their cognition and hence result in better prognosis.

Study design: The investigators will recruit 45 patients with ASD and gastrointestinal problems, aged 6-30 years, who are willing to receive FMT and 1-year regular follow-up. The investigators will collect demographic data, blood and stool samples before and after the intervention, and analyze changes of intestinal microbiota and cytokines. The investigators will use subjective questionnaires to evaluate gastrointestinal, autistic, emotion and behavior symptoms, and objective measurements including actigraphy, intelligence and attention tests to evaluate changes in sleep and cognitive functions. The investigators will analyze the correlations between collected variables and compare the ASD group with the healthy control group at baseline to evaluate group differences. The investigators will evaluate the differences of the intervention group before and after FMT, and also compare the intervention group with the waiting list group, to evaluate the efficacy of FMT. Variables will be presented by mean and percentage. The investigators will use independent sample t-test or Chi-squared test for group comparison. The efficacy of FMT will be analyzed by dependent sample t-test or Wilcoxon signed-rank test, and the investigators will use Pearson correlation coefficient to analyze the correlations between variables.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed by a child psychiatrist in line with DSM-5 Autism Spectrum Disorder
  • Combined with gastrointestinal problems, any Gastrointestinal Symptoms Rating Scale score≧3.
  • Age is between 7-30.
  • Participants who are willing to participate in the study and sign the informed consent.

Exclusion criteria

  • Cases where clinical assessment cannot cooperate with fecal microbiota transplantation and examination.
  • Cases requiring antibiotics within 3 months before or after acceptance because of their physiological condition.
  • Cases requiring long-term use of proton pump inhibitors due to their physiological conditions.
  • Severe physical diseases, such as acute gastrointestinal diseases, severe malnutrition or underweight, immunodeficiency diseases, severe allergies or autoimmune diseases, brain injuries or severe organic brain diseases, will affect the evaluation of treatment results.
  • Severe mental illness, such as schizophrenia, bipolar disorder, etc.
  • Those who used probiotics one month before the case may affect the intestinal flora.
  • Pregnancy.
  • Cases that cannot understand the content of this research.
  • Participants who are unwilling to participate in the study or refuse to sign the informed consent.
  • Participants who are not suitable to include in this study, evaluate by PI or Co-PI.

Treatment and study plan

Fecal Microbiota Transplantation

Procedure

Fecal microbiota transplantation has been applied to patients with autism spectrum disorder in recent years. Fecal microbiota of healthy donors can be transplanted to patients through colonoscopy. Before donation, donors were comprehensively screened to rule out gastrointestinal symptoms and infections. Patients will receive colon preparation before transplantation. After the intervention, patients will have to stay in bed and be monitored for 24 hours to assure safety.

Primary outcomes

  1. Changes of gastrointestinal symptoms of patients with ASD after FMT

    Time frame: baseline and the 1-year follow-up

    the Gastrointestinal Symptom Rating Scale, score 15-105, higher scores mean more severe symptom

  2. Changes of autistic symptoms of patients with ASD after FMT

    Time frame: baseline and the 1-year follow-up

    the Social Responsiveness Scale, score 0-195, higher scores mean more severe symptom

Secondary outcomes

  1. Changes of the diversity of intestinal microbiota of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    microbial DNA was extracted from feces by Reagent Kit v3, and the diversity indices were calculated by using the vegan package in R version 3.2.3. higher indices suggest higher microbial diversity

  2. Changes of cytokine levels of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    cytokine levels

  3. Changes of repetitive behavior symptoms of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Repetitive Behavior Scale-Revised data, higher score suggest more repetitive behavior

  4. Changes of autistic behavior symptoms of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Aberrant Behavior Checklist data, higher score suggest more autistic behavior

  5. Changes of emotion and behavior symptoms of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Child Behavior Checklist Adaptive Behavior Assessment System® - Second Edition data, higher score suggest more emotion and behavior symptoms

  6. Changes of inattention and hyperactivity of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Swanson, Nolan and Pelham IV Scale data, higher score suggest worse attention and more hyperactivity

  7. Changes of quality of life of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the 36-Item Short Form Health Survey data, higher score suggest better quality of life

Other outcomes

  1. Changes of objective sleep of patients with ASD after FMT by actigraphy recording

    Time frame: baseline and the 1 year follow-up

    Participants wear actigraphy for 7-10 days to record their activities and light exposure, which can be calculated to represent their sleep patterns. Sleep parameters including (total sleep time: minutes, sleep efficiency: percentage, total time in bed: minutes, sleep onset latency: minutes, wakefulness after sleep onset: minutes, the sum of wake duration overnight: minutes, total number of awakenings: times, sleep onset time and wake time: hours and minutes) will be obtained and analyzed.

  2. Changes of subjective sleep of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Children's Sleep Habits Questionnaire data, higher score suggest poorer sleep

  3. Changes of intelligence of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Wechsler Intelligence Scale data, higher score suggest better intelligence

  4. Changes of attention and impulse control of patients with ASD after FMT

    Time frame: baseline and the 1 year follow-up

    the Conners' Continuous Performance Test data, higher score suggest worse attention and impulse control

Study contacts

Contact information is provided by the study sponsor or research team.

Wei-Chih Chin

CONTACT

[email protected]

+886 3 3281200 ext. 3836

Sponsors and collaborators

Lead sponsor

Chang Gung Memorial Hospital

Other

Registry information

Official study title

Fecal Microbiota Transplantation for Gastrointestinal, Autistic, Emotion, and Behavior Symptoms of Patients With Autism Spectrum Disorder and Gastrointestinal Problems: a Preliminary Study.

Important dates

Study start
2024
Primary completion
2027
Study completion
2027
First posted
Mar 4, 2024
Registry last updated
Mar 20, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.