Internet therapy for children with abdominal pain
Individualized Online Cognitive Behavioral Therapy for Children With Functional Abdominal Pain Disorders - the Child's Pain Regulation
This study is testing if online therapy can help children aged 8-17 with stomach pain feel better by looking at how their pain management changes during treatment.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 80 (estimated) |
| Ages | 8 Years to 17 Years |
| Sex | All |
| Sponsor | Karolinska Institutet Academic / other |
| Locations | 1 site (Stockholm, Karolinska Institutet) |
| Trial ID | NCT05945251 on ClinicalTrials.gov |
What this trial studies
This observational study focuses on children aged 8-17 with Functional Abdominal Pain Disorders (FAPDs) to evaluate their pain regulation compared to healthy controls. It aims to determine how aspects of pain regulation relate to improvements in symptoms for those engaging in Internet-delivered cognitive behavioral therapy (Internet-CBT). The study will also assess whether any changes in pain regulation occur during the treatment process. By understanding these dynamics, the study seeks to enhance treatment outcomes for children suffering from FAPDs.
Who should consider this trial
Good fit: Ideal candidates are children aged 8-17 diagnosed with Functional Abdominal Pain Disorders who have been offered treatment at BUP Internetbehandling.
Not a fit: Patients who do not have recurrent or persistent abdominal pain and those with contraindications for MR will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment strategies for children with abdominal pain, enhancing their quality of life.
How similar studies have performed: Other studies have shown promise in using cognitive behavioral therapy for similar conditions, suggesting potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: Children 8-17 years with FAPDs: Have been offered treatment at BUP Internetbehandling for FAPDs. Children 8-17 years without FAPDs: Not affected by recurrent (every week) or persistant pain during the last year. Exclusion Criteria: Contraindication for MR (metal implant or metal object in body, claustrophobia, pregnancy)
Where this trial is running
Stockholm, Karolinska Institutet
- Karolinska Institutet — Stockholm, Karolinska Institutet, Sweden (Recruiting)
Study contacts
- Principal investigator: Maria Lalouni, PhD — Karolinska Institutet
- Study coordinator: Maria Lalouni, PhD
- Email: maria.lalouni@ki.se
- Phone: +46709473148
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.