Internet-delivered Cognitive Behavior Therapy for Adolescents With Functional Gastrointestinal Disorders: a Pilot Study

Not Applicable

Completed

• Conditions: Irritable Bowel Syndrome; Functional Gastrointestinal Disorders
• Interventions: Behavioral: Internet-delivered CBT

• Registration Number: NCT02033161
• Lead Sponsor: Karolinska Institutet

Brief Summary

This pilot-study aims to evaluate the treatment effects and feasibility of an internet-delivered CBT-program for adolescents with functional gastrointestinal disorders.

Detailed Description

Functional gastrointestinal disorders (FGID), including irritable bowel syndrome (IBS), functional dyspepsia (FD) and functional abdominal pain (FAP), are common in adolescents and associated with impaired quality of life. In adults with IBS, internet-delivered CBT leads to reduced symptoms and increased quality of life, but studies in children are lacking. This pilot-study aim to evaluate the treatment effects and feasibility of an internet-delivered CBT-program for adolescents with FGID.

Method: Pilot study with a pre-post-design and no control group. The internet-delivered CBT-program lasted for 8 weeks and included weekly therapist support, consisting of online messages and telephone calls. Assessment points were baseline, post-treatment and 6 months follow-up.

Analysis: Effect sizes and within-group differences were calculated in an intent-to-treat analysis using Cohens' d and Student's t-test.

Study Timeline

• Study Start: 2012-03
• Primary Completion: 2013-06
• Study Completion: 2013-06
• Study First Submitted: 2013-12-05
• Status Verified: 2014-01
• Study First Submitted QC: 2014-01-09
• Last Update Submitted: 2014-01-09
• Study First Posted: 2014-01-10
• Last Update Posted: 2014-01-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 29

Inclusion Criteria

• age between 13 and 17 years old.
• a diagnosis of a functional gastrointestinal disorder by treating physician, e.g. IBS, FD or FAP.
• adolescent and one parent should have easy access to the Internet, some computer experience and good Swedish language skills.

Exclusion Criteria

• concurrent serious medical conditions or gastrointestinal symptoms likely caused by an organic disorder.
• psychiatric diagnosis more urgent to treat than the abdominal pain.
• on-going psychological treatment.
• absence from school more than 20%.
• on-going maltreatment, violence or severe parental psychiatric illness in the family.
• pronounced language and learning difficulties depending on whether the youth was expected to benefit from the treatment or not.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Internet-delivered CBT	Internet-delivered CBT	-

Primary Outcome Measures

Name	Time	Method
Change in gastrointestinal symptoms from baseline to 8 weeks, and from baseline to 6 months after treatment.	Baseline to 8 weeks, baseline to 8 months.	Measured with a self-report scale, GSRS-IBS, that have 13 items about weekly gastro-intestinal symptoms like bloating, hard stool, abdominal pain etc. It is a seven-point Likert scale, from 1 ("no trouble at all") to 7 ("very severe discomfort"). The GSRS-IBS has excellent psychometric properties with internal consistency between α = .74 (for abdominal pain) to α = .85 (for satiety).

Secondary Outcome Measures

Name	Time	Method
Change in pain reactivity from baseline to 8 weeks, and from baseline to 6 months after treatment.	Baseline to 8 weeks, baseline to 8 months.	Measured with a self-report scale, pain reactivity scale (PRS), that have 5 items about reactivity to and worry about pain. Three items are about emotional reactions to current pain. Two items affect frequency of worry about not being able to do things now, and in the future because of the pain. Questions are answered on a 6-point scale from 0 ("not at all") to 6 ("very much"). PRS has been reported to have satisfactory psychometric properties (Wicksell et al, 2011).
Change in pain interference on activities from baseline to 8 weeks, and baseline to 6 months after treatment.	Baseline to 8 weeks, baseline to 8 months.	Measured with a self-report scale, pain interference index (PII), that have 6 items about interference on various activities because of pain. Questions are answered on a 6-point scale from 0 ("not at all") to 6 ("very much"). According to preliminary analysis, the instrument has satisfactory psychometric properties (Wicksell et al., 2011)
Change in function from baseline to 8 weeks and from baseline to 6 months after treatment.	Baseline to 8 weeks, baseline to 8 months.	Measured with a self-report scale, functional disability index (FDI), with 15 items on daily activities. Questions are related to specific activities such as climbing stairs, running 100 meters and to go shopping, and general activities such as eating meals and being in school all day. The scale ranges from 1 (no problem at all) to 5 (impossible). It is validated for children and adolescents with chronic abdominal pain with high internal consistency, α = .86 for boys and α = .91 for girls (Claar and Walker, 2006). FDI is the scale that is recommended in pediatric pain studies to measure the influence of pain on function (McGrath et al., 2008).
Change in sensitivity to symptoms of anxiety from baseline to 8 weeks, and from baseline to 6 months after treatment.	Baseline to 8 weeks, baseline to 8 months.	Measured by a self-report scale called Childhood Anxiety Sensitivity Index (CASI) with 18 items. It is a 3-point scale (1-3), which measures sensitivity to internal sensations that could be symptoms of anxiety. The questions include items such as "I get scared when I feel shaky" or "I get scared when my heart beats fast" but also items that could be gastro-intestinal symptoms, such as "When my stomach hurts, I worry that i might be really sick "(Silverman, Fleisig, Rabian, \& Peterson, 1991). CASI has been reported to have high reliability, α = .84 (Silverman et al. 1991).
Change in level of depression from baseline to 8 weeks and from baseline to 6 months after treatment.	Baseline, 8 weeks and 8 months.	Measured by the self-report scale Child depression Inventory (CDI) that consists of 27 items on a 3-graded scale (0-2). The scale's psychometric properties have been validated in a study by Smucker, Craighead and Green (1986), which found that the internal consistency measured by Cronbach's alpha was acceptable, between α = .83 and α = .89.
Change in level of perceived stress from baseline to 8 weeks and from baseline to 6 months after treatment.	Baseline, 8 weeks and 8 months.	Measured by a four-item short version of a self-report scale, Percieved Stress Scale (PSS-4). PSS-4 consists of four statements about the feeling of being able to control and sort out problems that need to be managed. Responses are rated from 0 ("never") to 4 ("very often"). Reliability for the version with 4 items is α = .72 (Cohen et al., 1983).

Trial Locations

Locations (1)

Child and Adolescent Psychiatry; 🇸🇪 Stockholm, Sweden