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Clinical Trials/NCT02903030
NCT02903030
Completed
Early Phase 1

Probiotics for Quality of Life in Autism Spectrum Disorders

Ohio State University1 site in 1 country13 target enrollmentAugust 2016

Overview

Phase
Early Phase 1
Intervention
Maltose (placebo)
Conditions
Autism Spectrum Disorders
Sponsor
Ohio State University
Enrollment
13
Locations
1
Primary Endpoint
Change in Gastrointestinal (GI) Module of the Pediatric Quality of Life Inventory (PedsQL) at From Baseline at Week 8
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

A randomized pilot trial of a probiotic for quality of life in autism spectrum disorder (ASD), targeting gastrointestinal (GI) symptoms.

Detailed Description

The physical and mental/emotional health of people with autism spectrum disorder (ASD) are closely connected. The emerging data on immune abnormalities and gut microbiome differences, and interactions of the genome with these suggest a possible etiological link between physical and mental dysfunction, especially the gastrointestinal (GI) dysfunction and severe anxiety that many individuals with ASD manifest. The investigators have preliminary clinical evidence that children with ASD \& GI symptoms differ in microbiome composition and function from neurotypical children with GI symptoms. The investigators hypothesize that altered host-microbial signals, which include altered fecal neurotransmitter gamma-aminobutyric acid (GABA) levels contribute towards anxiety and sensory over-responsivity in ASD. Our preliminary findings also show that probiotic Visbiome Extra Strength, improves GI and pain symptoms, correlating with altered gut microbiome composition and related metabolites (the macrobiome). The proposed crossover trial will explore the possibilities of this new appreciation of the microbiome-mental/physical function connection for ASD, GI dysfunction, and anxiety. If altering the gut microbiome results in better GI and emotional function, it could improve the quality of life for children with ASD and their parents. A pilot trial with 12 children with ASD will test feasibility for a proposed three-site crossover randomized clinical trial (RCT) of probiotics (beneficial bacteria including Lactobacilli \& Bifidobacteria) in 60 children 3-12 years old with ASD, GI dysfunction, \& anxiety. In a balanced crossover children will be randomized 1;1 to Visbiome or placebo first, 8 weeks per condition with 3 weeks washout between. The investigators have access to significant fecal microbiome and metabolome data from NIH-funded Human Microbiome Projects (HMP) on similar-age healthy and irritable-bowel children, with and without ASD. These will help leverage our understanding of macrobiome changes that correlate with functional improvement of GI and abdominal pain symptoms. Pilot study efficiency will also benefit from those HMPs having already collected and analyzed baseline stools for some children with ASD, thus saving significant costs for baseline stool analyses for the pilot.

Registry
clinicaltrials.gov
Start Date
August 2016
End Date
December 1, 2017
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

L. Eugene Arnold

Professor Emeritus of Psychiatry

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • have DSM-5 ASD on clinical evaluation by a doctoral-level diagnostician, confirmed by Autism Diagnostic Interview-Revised or Autism Diagnostic Observation Schedule;
  • be between 3 and 12 years old;
  • have \>2 mo. abdominal pain, constipation, diarrhea, and/or vomiting, with an item-mean score \>2 on at least one scale of the GI module of the PedsQL scale;
  • have clinical anxiety symptoms with an item mean of \>1.0 (0-3 scale) on the new Autism Anxiety Scale.
  • Participants will be recruited from minority, poor, inner city, or rural populations.

Exclusion Criteria

  • Antibiotics in 2 months prior to enrolling;
  • Prior bowel surgery;
  • Chronic serious medical condition (e.g., diabetes);
  • Weight or height \< 3rd %ile for age;
  • Chronic anti-inflammatory use within 2 months prior to enrolling;
  • History of inflammatory bowel disease, Celiac disease, or eosinophilic disorders (e.g., eosinophilic esophagitis);
  • Already taking probiotics within the previous 6 months.

Arms & Interventions

Placebo, Then Visbiome

Placebo matched to probiotic.

Intervention: Maltose (placebo)

Visbiome, Then Placebo

The probiotic mix (VISBIOME) will be mainly Bifidobacteria and Lactobacilli, in view of the previously reported encouraging clinical studies and safety data.

Intervention: Visbiome Extra Strength

Outcomes

Primary Outcomes

Change in Gastrointestinal (GI) Module of the Pediatric Quality of Life Inventory (PedsQL) at From Baseline at Week 8

Time Frame: Baseline and Week 8 of Both the First and Second Intervention

A 74-item survey with 14 scales. Report forms for specific age ranges assess the parent's perception of the child's GI function and/or symptoms during the last month on a 5-point scale from 0 (never a problem) to 4 (almost always a problem). Items are reverse-scored and transformed to a 0-100 scale so lower scores reflect worse GI dysfunction. Response choices are in Likert-scale format ranging from 0 to 4 (0=Never, 1=Almost Never, 2=Sometimes, 3=Often, 4=Almost Always).

Secondary Outcomes

  • Change in The Aberrant Behavior Checklist (ABC) From Baseline at Week 8(Baseline and Week 8 of Both the First and Second Intervention)
  • Children's Sleep Habits Questionnaire (CSHQ) at Week 8(Week 8 of Both the First and Second Intervention)
  • Change in Parent Anxiety Checklist--ASD From Baseline at Week 8(Baseline and Week 8 of Both the First and Second Intervention)
  • Change in Social Responsiveness Scale (SRS) From Baseline at Week 8(Baseline and Week 8 of Both the First and Second Intervention)
  • Change in Target Symptom Rating From Baseline at Week 8(Baseline and Week 8 of Both the First and Second Intervention)
  • Change in The Parenting Stress Index Short Form (PSI)(Baseline and Week 8 of Both the First and Second Intervention)

Study Sites (1)

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