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Probiotic Supplementation in Children With ADHD

Primary Purpose

ADHD

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Experimental: Kefir probiotic drink (supplied by Nourish)
Placebo comparator
Sponsored by
St. Mary's University, Twickenham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for ADHD focused on measuring microbiome, ADHD, probiotic, Kefir

Eligibility Criteria

8 Years - 13 Years (Child)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • A previous diagnosis of ADHD according to the DSM-IV or DSM-V criteria by a qualified health care professional.
  • Children aged between 8 and 13 years at the time of study.
  • Children with a comorbidity will be accepted.
  • Both males and females

Exclusion Criteria:

  • Children currently undergoing a current course of behavioural therapy.
  • Children currently on ADHD medication (such as methylphenidate) at the time of the study.
  • Children with a reported milk allergy or lactose intolerance.
  • Reported use of antibiotics, probiotics, antifungals or steroids in the past four weeks.
  • Diagnosis of a gastrointestinal disorder e.g., Inflammatory Bowel Disease or Coeliac disease.
  • Diagnosis of an auto-immune disease or compromised immunity.

Sites / Locations

  • St Mary's University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Kefir probiotic drink

placebo comparator

Arm Description

Daily kefir for 6 weeks.

Daily non-fermented dairy based equivalent drink for 6 weeks.

Outcomes

Primary Outcome Measures

Change in The Strengths and Weakness of ADHD-symptoms and Normal-behaviour (SWAN) scale
18 item scale comparing the child to other children of the same age. Each item is responded to on a seven-point scale ranging from far below average (-3) to far above average (+3). The scores are summed and divided by the number of items, to express the summary score as the average rating-per-item (range -3 to +3, with lower scores indicating more severe ADHD symptoms).

Secondary Outcome Measures

Change in The Go/NoGo test
Participants respond to a particular stimulus while various stimuli are presented on a computer screen. There are 1500 milliseconds between each response, with 320 repetitions. Go errors (errors of omission) - A higher score = greater inattention (worse) NoGo errors (errors of commission) - A higher score = greater impulsivity (worse) Go reaction times - A higher score = less impulsivity (better) Go reaction time variability - A higher score = greater inattention (worse)
Change in mean activity during sleep.
Actigraphy recordings. Range 0-∞. A higher score = less sound sleep (worse).
Change in minutes spent awake during the down period
Actigraphy recordings. Range 0-∞. A higher score = less sound sleep (worse).
Change in sleep latency
Actigraphy recordings of time taken to fall asleep. Range 0-∞. A higher score = more time taken to fall asleep (worse).
Change in sleep efficiency
Actigraphy recordings of % down period spent asleep, after removing sleep latency. A higher score = better.
Change in wake after sleep onset
Actigraphy recordings of minutes spent awake during the down period after removing sleep latency. Range 0-∞. A higher score = less sound sleep (worse).
Change in sleep fragmentation
Actigraphy recordings of the number of awakenings/ total minutes of sleep x 100) - Higher score = more fragmented sleep (worse).
Change in mean daytime activity
Actigraphy recording of mean daytime activity. (0-∞) not necessarily worse or better.
The Consensus Sleep diary
Record of sleep - used qualitatively to detect and remove artefacts from the data. Takes approximately 3 minutes per day to complete.
The Consensus Sleep diary
Record of sleep - used qualitatively to detect and remove artefacts from the data. Takes approximately 3 minutes per day to complete.
Change in The Child's Sleep habits questionnaire
Consists of 33 items. Each item is rated by parents using a three-point scale (with some items reverse-scored): 3 - Usually =occurs 5+ times a week 2 - Sometimes = occurs 2-4 times a week 1 - Rarely = occurs 0-1 times a week A Total Sleep Disturbances score is calculated as the sum of all scored questions. Total scores range from 33 to 99 - higher scores indicate more problematic sleep.
Change in Sleep self report
Consists of 26 items. Each item is rated by children using a three-point scale (with some items reverse-scored): 3 - Usually = occurs 5+ times a week 2 - Sometimes = occurs 2-4 times a week 1 - Rarely = occurs 0-1 times a week. A Total Sleep Disturbances score is calculated as the sum of all scored questions. Total scores range from 26 to 78 - higher scores indicate more problematic sleep.
Change in The Gastrointestinal Severity Index
A three-point rating scale across six gastrointestinal symptoms. A higher scores indicate worse symptoms. Total scores range from 0-12 - higher scores indicating more severe symptoms.
Change in stool microbiome analysis
Investigate if there are changes in diversity and species in week 6 relative to week 0.

Full Information

First Posted
November 11, 2021
Last Updated
September 26, 2023
Sponsor
St. Mary's University, Twickenham
Collaborators
Goldsmiths, University of London, London South Bank University
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1. Study Identification

Unique Protocol Identification Number
NCT05155696
Brief Title
Probiotic Supplementation in Children With ADHD
Official Title
A Randomised Controlled Trial of the Effects of a Probiotic Drink on Behaviour, Sleep and the Microbiome in Children With ADHD
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Completed
Study Start Date
January 6, 2022 (Actual)
Primary Completion Date
September 26, 2023 (Actual)
Study Completion Date
September 26, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Mary's University, Twickenham
Collaborators
Goldsmiths, University of London, London South Bank University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This randomised, placebo controlled trial explores the effects of supplementation with a probiotic drink (kefir) in children diagnosed with ADHD on behaviour, sleep, attention and the gut microbiome.
Detailed Description
Children with Attention Deficit Hyperactivity Disorder (ADHD) can suffer debilitating symptoms, including problematic behaviour and sleep. Dietary manipulations may be a helpful treatment option for children, but the most effective are highly restrictive, with little known about why they might work. Optimising gut bacteria may help alleviate some of the symptoms of this condition via the gut-brain-axis. The consumption of a probiotic fermented drink (kefir) can positively influence composition of gut bacteria. The purpose of this study is to explore the effects of supplementation of a probiotic drink (kefir) on behaviour, sleep, attention and the gut microbiome in children diagnosed with ADHD. In a six-week randomised controlled double-blind, placebo controlled trial, 70 children diagnosed with ADHD (aged 8-13 years) will be randomised to be given either a probiotic drink (kefir) or a placebo drink. At the beginning and the end of the study a combination of questionnaires, cognitive assessment, sleep/physical activity measures and microbiome analysis will be employed to assess the effect of kefir consumption on symptoms of ADHD and the gut microbiome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
ADHD
Keywords
microbiome, ADHD, probiotic, Kefir

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomised double-blind quantitative repeated measures design
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
a randomly generated 6-digit participant code will be allocated to each participant as a unique identifier for all data collection.
Allocation
Randomized
Enrollment
81 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Kefir probiotic drink
Arm Type
Experimental
Arm Description
Daily kefir for 6 weeks.
Arm Title
placebo comparator
Arm Type
Placebo Comparator
Arm Description
Daily non-fermented dairy based equivalent drink for 6 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Experimental: Kefir probiotic drink (supplied by Nourish)
Intervention Description
125ml per day of dairy based probiotic drink (Kefir) containing ≥ 50billion colony forming units (CFU), supplied in plain packaging.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo comparator
Intervention Description
125ml of non-fermented dairy based placebo (UHT milk) per day, supplied in plain packaging.
Primary Outcome Measure Information:
Title
Change in The Strengths and Weakness of ADHD-symptoms and Normal-behaviour (SWAN) scale
Description
18 item scale comparing the child to other children of the same age. Each item is responded to on a seven-point scale ranging from far below average (-3) to far above average (+3). The scores are summed and divided by the number of items, to express the summary score as the average rating-per-item (range -3 to +3, with lower scores indicating more severe ADHD symptoms).
Time Frame
week 0 and week 6
Secondary Outcome Measure Information:
Title
Change in The Go/NoGo test
Description
Participants respond to a particular stimulus while various stimuli are presented on a computer screen. There are 1500 milliseconds between each response, with 320 repetitions. Go errors (errors of omission) - A higher score = greater inattention (worse) NoGo errors (errors of commission) - A higher score = greater impulsivity (worse) Go reaction times - A higher score = less impulsivity (better) Go reaction time variability - A higher score = greater inattention (worse)
Time Frame
week 0 and week 6
Title
Change in mean activity during sleep.
Description
Actigraphy recordings. Range 0-∞. A higher score = less sound sleep (worse).
Time Frame
week 0 and week 6
Title
Change in minutes spent awake during the down period
Description
Actigraphy recordings. Range 0-∞. A higher score = less sound sleep (worse).
Time Frame
week 0 and week 6
Title
Change in sleep latency
Description
Actigraphy recordings of time taken to fall asleep. Range 0-∞. A higher score = more time taken to fall asleep (worse).
Time Frame
week 0 and week 6
Title
Change in sleep efficiency
Description
Actigraphy recordings of % down period spent asleep, after removing sleep latency. A higher score = better.
Time Frame
week 0 and week 6
Title
Change in wake after sleep onset
Description
Actigraphy recordings of minutes spent awake during the down period after removing sleep latency. Range 0-∞. A higher score = less sound sleep (worse).
Time Frame
week 0 and week 6
Title
Change in sleep fragmentation
Description
Actigraphy recordings of the number of awakenings/ total minutes of sleep x 100) - Higher score = more fragmented sleep (worse).
Time Frame
week 0 and week 6
Title
Change in mean daytime activity
Description
Actigraphy recording of mean daytime activity. (0-∞) not necessarily worse or better.
Time Frame
week 0 and week 6
Title
The Consensus Sleep diary
Description
Record of sleep - used qualitatively to detect and remove artefacts from the data. Takes approximately 3 minutes per day to complete.
Time Frame
week 0 and week 6
Title
The Consensus Sleep diary
Description
Record of sleep - used qualitatively to detect and remove artefacts from the data. Takes approximately 3 minutes per day to complete.
Time Frame
week 6
Title
Change in The Child's Sleep habits questionnaire
Description
Consists of 33 items. Each item is rated by parents using a three-point scale (with some items reverse-scored): 3 - Usually =occurs 5+ times a week 2 - Sometimes = occurs 2-4 times a week 1 - Rarely = occurs 0-1 times a week A Total Sleep Disturbances score is calculated as the sum of all scored questions. Total scores range from 33 to 99 - higher scores indicate more problematic sleep.
Time Frame
week 0 and week 6
Title
Change in Sleep self report
Description
Consists of 26 items. Each item is rated by children using a three-point scale (with some items reverse-scored): 3 - Usually = occurs 5+ times a week 2 - Sometimes = occurs 2-4 times a week 1 - Rarely = occurs 0-1 times a week. A Total Sleep Disturbances score is calculated as the sum of all scored questions. Total scores range from 26 to 78 - higher scores indicate more problematic sleep.
Time Frame
week 0 and week 6
Title
Change in The Gastrointestinal Severity Index
Description
A three-point rating scale across six gastrointestinal symptoms. A higher scores indicate worse symptoms. Total scores range from 0-12 - higher scores indicating more severe symptoms.
Time Frame
week 0 and week 6
Title
Change in stool microbiome analysis
Description
Investigate if there are changes in diversity and species in week 6 relative to week 0.
Time Frame
week 0 and week 6

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
13 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: A previous diagnosis of ADHD according to the DSM-IV or DSM-V criteria by a qualified health care professional. Children aged between 8 and 13 years at the time of study. Children with a comorbidity will be accepted. Both males and females Exclusion Criteria: Children currently undergoing a current course of behavioural therapy. Children with a reported milk allergy or lactose intolerance. Reported use of antibiotics, probiotics, antifungals or steroids in the past four weeks. Diagnosis of a gastrointestinal disorder e.g., Inflammatory Bowel Disease or Coeliac disease. Diagnosis of an auto-immune disease or compromised immunity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kate Lawrence, PhD
Organizational Affiliation
St. Mary's University, Twickenham
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Mary's University
City
London
State/Province
Greater London
ZIP/Postal Code
TW1 4SX
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
anonymised data will be made available on an open access repository.
IPD Sharing Time Frame
Study protocol and Statistical analysis plan available as soon as protocol is published - no end date to availability.
IPD Sharing Access Criteria
Open Access

Learn more about this trial

Probiotic Supplementation in Children With ADHD

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