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Collaborative Cognitive Behavioral Therapy / Hypnotherapy for Treatment of Pediatric Functional Gastrointestinal Disease (CAPP)

Primary Purpose

Irritable Bowel Syndrome (IBS)

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CBT/ Hypnotherapy
Routine Management
Sponsored by
Seton Healthcare Family
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Irritable Bowel Syndrome (IBS)

Eligibility Criteria

8 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 8 - 18
  • Meets Rome III Criteria for Pediatric Irritable Bowel Syndrome

    • Abdominal discomfort or pain associated with 2 or more of the following at least 25% of the time
    • Improved with defecation
    • Onset associated with a change in frequency of stool
    • Onset associated with a change in form of the stool
    • No evidence of inflammatory, anatomic, metabolic, or neoplastic process that explains the subject's symptoms
    • Criteria fulfilled once per week for at least 2 months before diagnosis

Exclusion Criteria: Unwillingness / Inability to engage in cognitive behavioral therapy arm of study (weekly encounters with psychologist)

Sites / Locations

  • 'Specially for Children, Dell Children's Medical Center of Central Texas

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Routine Management

CBT/ Hypnotherapy

Arm Description

All patients will be given a prescription for the use of antispasmodics. If patients demonstrate symptoms consistent with constipation predominant IBS they will be treated with laxatives. If symptoms are more consistent with diarrhea predominant IBS they will be treated with bulking agents (fiber) +/- antibiotics. Patient will be called every week while enrolled in the study in order to titrate doses, and answer questions.

The CBT (cognitive behavior therapy) program will consist of 7 sessions that will encompass the following skills of Symptom monitoring, Stress Management, Coping Skills, Relaxation training, Problem solving, and Cognitive Restructuring.The hypnotherapy program will be modeled after the North Carolina Standardized Hypnosis Treatment for Irritable Bowel Syndrome

Outcomes

Primary Outcome Measures

Functional Disability Inventory (FDI)
The FDI is a measure of the degree to which children experience difficulty in physical and psychosocial functioning due to their physical health status. Respondents are asked to rate how much physical difficulty was perceived for a variety of everyday activities. Both child-report and parent-report versions are composed of 15 questions.

Secondary Outcome Measures

Pain Beliefs Questionnaire
The Pain Beliefs Questionnaire is a 32-item measure assessing characteristic appraisals of pediatric abdominal pain severity (primary coping appraisals) and characteristic appraisals of ability to cope with pediatric abdominal pain (secondary coping appraisals).

Full Information

First Posted
September 19, 2013
Last Updated
May 17, 2019
Sponsor
Seton Healthcare Family
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1. Study Identification

Unique Protocol Identification Number
NCT01966341
Brief Title
Collaborative Cognitive Behavioral Therapy / Hypnotherapy for Treatment of Pediatric Functional Gastrointestinal Disease
Acronym
CAPP
Official Title
A Randomized Controlled Trial Comparing a Collaborative Cognitive Behavioral Therapy / Hypnotherapy Program to Standard Medical Management in the Treatment of Pediatric Functional Gastrointestinal Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Withdrawn
Why Stopped
Recruiting or enrolling participants has halted prematurely and will not resume
Study Start Date
April 2014 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Seton Healthcare Family

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This program has been created to help patients with irritable bowel syndrome manage their symptoms and increase their functioning by using cognitive therapy skills and hypnosis.
Detailed Description
Functional Gastrointestinal Diseases (FGID) are a family disorders that are characterized by gastrointestinal symptoms in the absence of readily identifiable organic pathology. Examples of FGID include irritable bowel syndrome, rumination syndrome, and function constipation. These disorders are classically thought to stem from dysfunction of the enteric nervous system. However, there is a growing recognition that multiple factors play a role in the genesis of FGIDs. This idea is encapsulated by the "biopsychosocial" model of disease, and is supported by a body of literature which has identified higher rates of FGID in patients with anxiety, depression, post-traumatic stress disorder, agoraphobia, and other psychosocial dysfunction. Recurrent Abdominal Pain and Irritable Bowel Syndrome are major causes of pediatric morbidity. Over a third of children and adolescents report recurrent abdominal pain, and the overall prevalence of non-organic abdominal pain has been noted to be over 75% 1 2. A large subset of these children report symptoms that are consistent with irritable bowel syndrome. Management of these children is complex and includes medical, dietary, and behavioral interventions. Medical therapy often revolves around the use of antispasmodics, probiotics, and antidepressants. The data supporting their use, however has been mixed. Over the last twenty years behavioral therapies such as cognitive behavioral therapy (CBT) and hypnotherapy (HT) have come to light as major treatment modalities for functional gastrointestinal disease. In a large multicenter randomized controlled trial Levy et al compared 3-session CBT to a control intervention and noted significant improvements and pain and function in children 3. Similar results have been published in multiple smaller trials 4-8. Likewise, Vlieger et al compared hypnotherapy to standard medical therapy in 53 children with irritable bowel syndrome. They found that, while both interventions resulted in improved pain scores, the hypnotherapy group demonstrated lasting clinical improvement at 1 year followup 9. Five year follow-up data has recently been published and revealed that significantly more of the hypnotherapy group remained in remission without any further intervention 10. A growing body of literature is available validating the use of hypnotherapy in irritable bowel syndrome in adults, and pain syndromes more generally 11-14. These therapies can be viewed as complementary to one another. CBT involves a very deliberate conscious understanding of ones disease process and triggers and focuses on successful pain mitigation measures. HT recruits the imagination with utilization of therapeutic imagery to down regulate inappropriate pain responses. Our center has developed a collaborative approach, utilizing both CBT and HT for the treatment of refractory IBS. To our knowledge no work has been done assessing the efficacy of such a collaborative approach using both CBT and HT in children with functional gastrointestinal disease. We therefore propose the following randomized case-control crossover trial to assess the efficacy our combined program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome (IBS)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Routine Management
Arm Type
Active Comparator
Arm Description
All patients will be given a prescription for the use of antispasmodics. If patients demonstrate symptoms consistent with constipation predominant IBS they will be treated with laxatives. If symptoms are more consistent with diarrhea predominant IBS they will be treated with bulking agents (fiber) +/- antibiotics. Patient will be called every week while enrolled in the study in order to titrate doses, and answer questions.
Arm Title
CBT/ Hypnotherapy
Arm Type
Experimental
Arm Description
The CBT (cognitive behavior therapy) program will consist of 7 sessions that will encompass the following skills of Symptom monitoring, Stress Management, Coping Skills, Relaxation training, Problem solving, and Cognitive Restructuring.The hypnotherapy program will be modeled after the North Carolina Standardized Hypnosis Treatment for Irritable Bowel Syndrome
Intervention Type
Behavioral
Intervention Name(s)
CBT/ Hypnotherapy
Intervention Description
The CBT program will consist of 7 sessions that will encompass the following skills of Symptom monitoring, Stress Management, Coping Skills, Relaxation training, Problem solving, and Cognitive Restructuring.The hypnotherapy program will be modeled after the North Carolina Standardized Hypnosis Treatment for Irritable Bowel Syndrome
Intervention Type
Drug
Intervention Name(s)
Routine Management
Other Intervention Name(s)
antispasmodics,laxatives,fiber,antibiotics.
Intervention Description
Treatment with use of antispasmodics,laxatives, and/or bulking agents (fiber) +/- antibiotics.
Primary Outcome Measure Information:
Title
Functional Disability Inventory (FDI)
Description
The FDI is a measure of the degree to which children experience difficulty in physical and psychosocial functioning due to their physical health status. Respondents are asked to rate how much physical difficulty was perceived for a variety of everyday activities. Both child-report and parent-report versions are composed of 15 questions.
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Pain Beliefs Questionnaire
Description
The Pain Beliefs Questionnaire is a 32-item measure assessing characteristic appraisals of pediatric abdominal pain severity (primary coping appraisals) and characteristic appraisals of ability to cope with pediatric abdominal pain (secondary coping appraisals).
Time Frame
10 weeks
Other Pre-specified Outcome Measures:
Title
Pain Response Inventory (PRI)
Description
The Pain Response Inventory (PRI) was developed as a multidimensional instrument to assess children's coping responses to recurrent pain
Time Frame
10 weeks
Title
Pain Frequency Score / Pain Intensity Score (PFS/PIS)
Description
Our primary outcome measure will be the PFS/PIS. It involves an aggregate score of pain intensity and frequency
Time Frame
10 weeks
Title
Abdominal Pain Index (API; Walker, Smith, Garber, & Van Slyke, 1997)
Description
Abdominal Pain Index comprises five items assessing the frequency, duration, and intensity of abdominal pain episodes experienced during the previous 2 weeks
Time Frame
10 weeks
Title
Children's Somatization Inventory (CSI)
Description
The CSI assesses a variety of nonspecific somatic symptoms
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
8 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 8 - 18 Meets Rome III Criteria for Pediatric Irritable Bowel Syndrome Abdominal discomfort or pain associated with 2 or more of the following at least 25% of the time Improved with defecation Onset associated with a change in frequency of stool Onset associated with a change in form of the stool No evidence of inflammatory, anatomic, metabolic, or neoplastic process that explains the subject's symptoms Criteria fulfilled once per week for at least 2 months before diagnosis Exclusion Criteria: Unwillingness / Inability to engage in cognitive behavioral therapy arm of study (weekly encounters with psychologist)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anees Siddiqui, MD
Organizational Affiliation
'Specially for Children, Dell Children's Medical Center of Central Texas
Official's Role
Principal Investigator
Facility Information:
Facility Name
'Specially for Children, Dell Children's Medical Center of Central Texas
City
Austin
State/Province
Texas
ZIP/Postal Code
78723
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Collaborative Cognitive Behavioral Therapy / Hypnotherapy for Treatment of Pediatric Functional Gastrointestinal Disease

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