Feasibility Study of a Guided Imagery Therapy Mobile Application for Functional Abdominal Pain Disorders in Children

Purpose

Chronic abdominal pain is common among children, and the majority of cases are attributed to functional abdominal pain disorders. One approach to treating these disorders is by using psychological therapies. This clinical trial aims to see how well pre-recorded guided imagery therapy sessions help children's abdominal pain when delivered via a mobile application (app) on a smartphone or tablet. Participants will complete a baseline abdominal pain and stooling diary to determine eligibility, as well as other surveys. Eligible participants will be given access to the guided imagery therapy mobile application. This intervention asks participants to listen to a 10- to 15-minute GIT session 5 out of 7 days per week for 8 weeks, in addition to their usual care for their abdominal pain. Then, participants will complete another abdominal pain and stooling diary, along with other psychometric surveys, at the end of this intervention period. Participants will also collect another diary and surveys 3 months post-treatment.

Conditions

  • Functional Abdominal Pain Disorders
  • Irritable Bowel Syndrome (IBS)
  • Functional Gastrointestinal Disorders (FGIDs)
  • Gastrointestinal and Digestive Disorder
  • Abdominal Pain/ Discomfort
  • Pain
  • Functional Dyspepsia

Eligibility

Eligible Ages
Between 7 Years and 12 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Texas Children's Pediatrics patients 7 to 12 years old at enrollment - A Rome IV Functional Abdominal Pain Disorder as defined by a 2-week abdominal pain and stooling diary - Both children and their primary caregivers must be able to read and communicate in English proficiently to understand the intervention's audio therapy sessions and psychometric instruments.

Exclusion Criteria

  • Previous abdominal surgeries - Co-morbid conditions associated with abdominal pain (e.g., cystic fibrosis) - Autism - Significant development delay - Psychosis - Prior experience with cognitive behavioral therapy or guided imagery therapy to treat chronic abdominal pain - Alarm symptoms that warrant further medical evaluation (e.g., blood in stool)

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Intervention Model Description
Qualified participants will be given access to the mobile app intervention for eight weeks. At the end of the eight weeks, outcome measures will be reassessed through an abdominal pain and stooling diary and other surveys. we will also assess these same outcomes 3 months -post-treatment.
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Treatment
Participants randomized to the Immediate Treatment arm will receive immediate access to the guided imagery therapy mobile application intervention.
  • Behavioral: Guided Imagery Therapy
    Participants will be asked to listen to a pre-recorded, 10 to 15 minute guided imagery therapy (GIT) sessions via mobile application 5 out of 7 days per week for 8 weeks in addition to their usual care for their abdominal pain.

Recruiting Locations

Baylor College of Medicine/Texas Children's Hospital
Austin, Texas 78759
Contact:
Hollier, MD
832-824-3814
jmhollie@bcm.edu

Baylor College of Medicine / Texas Children's Hospital
Houston, Texas 77030
Contact:
Hollier, MD
832-824-3814
jmhollie@bcm.edu

More Details

Status
Recruiting
Sponsor
Baylor College of Medicine

Study Contact

Hollier, MD
832-824-3814
GITgoStudy@bcm.edu

Detailed Description

After fully disclosing the study design, intervention options, randomization scheme, and potential side effects of the interventions, caregivers and their children will document their respective informed consent and assent electronically. REDCap is a secure web application designed for surveys and databases. All data captured through REDCap will be encrypted and transmitted securely to HIPAA-compliant institutional servers for storage. Participants and their caregivers will complete the following surveys at baseline, immediately post-therapy (8 weeks after baseline), and 3 months post-treatment through REDCap: - 2-week Abdominal Pain and Stooling Diary - Children's Somatic Symptoms Inventory (child self-report and parent proxy-report) - Pain Catastrophizing Scale - Child Version - Pain Catastrophizing Scale - Parent Version - Pediatric Quality of Life Inventory 4.0 Generic Core (child self-report and parent proxy-report) - Behavior Assessment System for Children 3rd Ed (child self-report and parent proxy-report)