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Reducing Pain and Anxiety Through Dietary Fiber Supplementation in Children With Abdominal Pain

Primary Purpose

Functional Abdominal Pain Syndrome

Status
Withdrawn
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Psyllium
Placebo
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Functional Abdominal Pain Syndrome focused on measuring Fiber, Psyllium, Quality of life, Gut microbiota, Anxiety, Pediatrics

Eligibility Criteria

8 Years - 16 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of functional abdominal pain as defined by the Rome IV criteria for childhood functional gastrointestinal disorders

Exclusion Criteria:

  • Diagnosis of inflammatory bowel disease or irritable bowel syndrome
  • Lactose intolerance
  • Abdominal surgery within the past year
  • Contraindications for imaging
  • Antibiotic use over the last 3 months

Sites / Locations

  • Pediatric GI Motility Laboratory at Alberta Children's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Psyllium

Placebo

Arm Description

For participants aged 8-11 and weighing > 24 kgs, the dosage is daily 3 grams for 2 weeks followed by daily 6 grams for 10 weeks. For children aged 12-16 and weighing > 40 kgs, the dosage is daily 5 grams for 2 weeks followed by daily 10 grams for 10 weeks.

For participants aged 8-11 and weighing > 24 kgs, the dosage is daily 3 grams for 2 weeks followed by daily 6 grams for 10 weeks. For children aged 12-16 and weighing > 40 kgs, the dosage is daily 5 grams for 2 weeks followed by daily 10 grams for 10 weeks.

Outcomes

Primary Outcome Measures

Change in abdominal pain scores as measured by an abdominal pain diary
The score minimum on the scale is 0, the maximum is 20. Higher scores indicate a worse outcome. The abdominal pain score diary is adapted from: See et al., 2001 - DOI: 10.1023/a:1010793408132

Secondary Outcome Measures

Anxiety scores as measured by PROMIS Anxiety scale
The Patient-Reported Outcomes Measurement Information System (PROMIS) questionaire will be used. The score minimum on the scale is 8, the maximum is 40. Higher scores indicate a worse outcome.
Quality of life as measured using the functional disability inventory (FDI)
The functional disability inventory (FDI) questionnaire will be used. The score minimum on the scale is 0, the maximum is 96. Higher scores indicate a worse outcome.

Full Information

First Posted
October 2, 2020
Last Updated
January 23, 2023
Sponsor
University of Calgary
Collaborators
Alberta Children's Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT04619095
Brief Title
Reducing Pain and Anxiety Through Dietary Fiber Supplementation in Children With Abdominal Pain
Official Title
Randomised, Blinded, Parallel, Placebo-controlled Study to Evaluate Whether Supplementation of the Dietary Fiber Psyllium Can Reduce Abdominal Pain and Improve Quality of Life and Anxiety in Children With Abdominal Pain.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Withdrawn
Why Stopped
We were unable to recruit any participants
Study Start Date
June 1, 2022 (Actual)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
November 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Calgary
Collaborators
Alberta Children's Hospital Research Institute

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
Background - Mental health and pain problems in early childhood are major risk factors for serious mental health problems into adulthood. These long-term effects point toward the essential need for prevention and early intervention to curbing the rising tide of global mental health disease. New approaches to child and adolescent mental health are urgently needed. This study focus on children with functional abdominal pain (FAP), which is defined as recurrent abdominal pain independent of bowel movements without an underlying medical cause. This population has a high co-occurrence of anxiety and somatic complaints. The effects of fiber on gastrointestinal pain have not yet been tested in this group. The investigators propose that supplementation with dietary fiber (psyllium) in children with FAP will promote SCFA production by the gut microbiota, reducing abdominal pain and subsequently anxiety and improving quality of life. Psyllium promotes SCFA production, is considered safe, and meta-analyses have identified it as the most potent fiber for reducing abdominal complaints in IBS patients, indicating strong potential for reducing abdominal pain in children with FAP. It is essential that potential mechanisms through which psyllium-induced SCFA production can reduce abdominal pain and anxiety symptoms and improve quality of life are explored. This study will explore 3 mechanisms: 1) activation of the vagus nerve, as SCFAs can induce vagal signalling, and evidence suggests that vagus nerve stimulation can reduce pain and anxiety symptoms; 2) reduction in HPA-axis responsiveness, since fiber has been shown to do so in adults, and both abdominal pain and anxiety disorders are associated with increased HPA-axis activity; and 3) structural and functional brain changes in the amygdala and hippocampus, as SCFA can influence neuronal activity of specific brain regions and probiotics-induced improvements in mental health have been related to these brain regions in adults with IBS. Research question & Objectives - The first objective is to provide a dietary fiber psyllium supplement to children (ages 8-16 years) who suffer from FAP. The aims are to: 1) determine whether psyllium reduces abdominal pain, 2) investigate whether this subsequently decreases anxiety and improves quality of life, and 3) assess associated gut-brain axis mediators, specifically the vagus nerve, HPA-axis, and brain networks. Methods - The investigators propose a 12-week placebo-controlled double-blind parallel-group intervention pilot study (n=20/group) where children suffering from FAP will receive a daily supplement of either psyllium or placebo (maltodextrin). For participants aged 8-11 and weighing > 24 kgs, the dosage is daily 3 grams for 2 weeks followed by daily 6 grams for 10 weeks. For children aged 12-16 and weighing > 40 kgs, the dosage is daily 5 grams for 2 weeks followed by daily 10 grams for 10 weeks. An initial lower dose was chosen to allow the gastrointestinal tract to acclimatize to the increase in dietary fiber. The dosages were chosen based on the fact that this age group typically consumes 10g less dietary fiber than recommended. All study measures are collected prior to, and after the intervention. The primary measure is abdominal pain frequency and intensity during 7 consecutive days. Secondary measures include parent and child reported anxiety and quality of life. Stool samples are used to determine gut microbiota and SCFAs. MRI will be used to assess the role of brain regions implicated in pain and anxiety. Respiratory sinus arrhythmia during seated rest will be used to assess basal vagal tone.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Functional Abdominal Pain Syndrome
Keywords
Fiber, Psyllium, Quality of life, Gut microbiota, Anxiety, Pediatrics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Psyllium
Arm Type
Experimental
Arm Description
For participants aged 8-11 and weighing > 24 kgs, the dosage is daily 3 grams for 2 weeks followed by daily 6 grams for 10 weeks. For children aged 12-16 and weighing > 40 kgs, the dosage is daily 5 grams for 2 weeks followed by daily 10 grams for 10 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
For participants aged 8-11 and weighing > 24 kgs, the dosage is daily 3 grams for 2 weeks followed by daily 6 grams for 10 weeks. For children aged 12-16 and weighing > 40 kgs, the dosage is daily 5 grams for 2 weeks followed by daily 10 grams for 10 weeks.
Intervention Type
Dietary Supplement
Intervention Name(s)
Psyllium
Intervention Description
See the information already included in the arm descriptions.
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
See the information already included in the arm descriptions.
Primary Outcome Measure Information:
Title
Change in abdominal pain scores as measured by an abdominal pain diary
Description
The score minimum on the scale is 0, the maximum is 20. Higher scores indicate a worse outcome. The abdominal pain score diary is adapted from: See et al., 2001 - DOI: 10.1023/a:1010793408132
Time Frame
Significant change from week-zero to week 12 between the active and placebo group
Secondary Outcome Measure Information:
Title
Anxiety scores as measured by PROMIS Anxiety scale
Description
The Patient-Reported Outcomes Measurement Information System (PROMIS) questionaire will be used. The score minimum on the scale is 8, the maximum is 40. Higher scores indicate a worse outcome.
Time Frame
Significant change from week-zero to week 12 between the active and placebo group
Title
Quality of life as measured using the functional disability inventory (FDI)
Description
The functional disability inventory (FDI) questionnaire will be used. The score minimum on the scale is 0, the maximum is 96. Higher scores indicate a worse outcome.
Time Frame
Significant change from week-zero to week 12 between the active and placebo group
Other Pre-specified Outcome Measures:
Title
Stool microbiome - Stool samples will be assayed using metagenome shotgun sequencing, after which alpha diversity is assessed.
Description
Alpha diversity will be assessed using the Shannon diversity index.
Time Frame
Significant change in alpha diversity from week-zero to week 12 between the active and placebo group
Title
Stool metabolome - Stool samples will be assayed using liquid chromatography-mass spectrometry for short-chain fatty acid levels
Description
Short-chain fatty acid levels are expressed as mM.
Time Frame
Significant change in short-chain fatty acid levels from week-zero to week 12 between the active and placebo group
Title
Respiratory sinus arrhythmia.This will be quantified using the high-frequency component of heart-rate variability.
Description
Vagus nerve activity will be measured indirectly using respiratory sinus arrhythmia.
Time Frame
Significant change from week-zero to week 12 between the active and placebo group
Title
Both structural and functional MRI will be used to quantify changes in connectivity between the amygdala and prefrontal cortex.
Description
Connectivity will be expressed as a z-score.
Time Frame
Significant change in amygdala-prefrontal cortex connectivity from week-zero to week 12 between the active and placebo group

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of functional abdominal pain as defined by the Rome IV criteria for childhood functional gastrointestinal disorders Exclusion Criteria: Diagnosis of inflammatory bowel disease or irritable bowel syndrome Lactose intolerance Abdominal surgery within the past year Contraindications for imaging Antibiotic use over the last 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerald Giesbrecht, PhD
Organizational Affiliation
Depts. of Paediatrics and Community Health Sciences, University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric GI Motility Laboratory at Alberta Children's Hospital
City
Calgary
State/Province
Alberta
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

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Reducing Pain and Anxiety Through Dietary Fiber Supplementation in Children With Abdominal Pain

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