Self-administered psychological programs for treating irritable bowel syndrome
Desarrollo de Programas de intervención psicológica Autoadministrable Con Soporte de Nuevas tecnologías Como Tratamiento Para Pacientes Con Trastornos Funcionales Digestivos.
NA · Hospital Universitari Vall d'Hebron Research Institute · NCT06318572
This study is testing whether virtual reality programs can help people with irritable bowel syndrome manage their symptoms and improve their overall well-being from the comfort of their homes.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Hospital Universitari Vall d'Hebron Research Institute (other) |
| Locations | 1 site (Barcelona) |
| Trial ID | NCT06318572 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of innovative psychological interventions delivered through virtual reality technology for patients suffering from functional digestive disorders, particularly irritable bowel syndrome. The approach focuses on using telematic methods to provide psycho-educational support at home, addressing symptoms severity, comorbidities, visceral sensitivity, and intestinal dysbiosis. By leveraging technology, the study seeks to overcome the barriers of limited access to traditional psychological therapies for these common conditions.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals with a BMI between 18.5-24.99 who can understand and follow instructions and have access to the internet.
Not a fit: Patients with a history of major psychiatric disorders or significant organic gastrointestinal pathology may not benefit from this study.
Why it matters
Potential benefit: If successful, this intervention could significantly improve the quality of life for patients with irritable bowel syndrome by providing accessible psychological support.
How similar studies have performed: Previous studies have shown that psychological interventions like cognitive behavioral therapy can be beneficial for managing similar disorders, indicating a promising avenue for this novel approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * BMI (Body Mass Index) between 18.5-24.99, with variations of up to 15%. * Ability to understand instructions and follow protocol. * Access to internet network from usual residence. Exclusion Criteria: * Previous history of abdominal surgery with the exception of appendectomy and herniorrhaphy. * Abuse of alcohol, tobacco or narcotics. * Medical evidence of organic gastrointestinal pathology, hepatopathy, endocrinopathy, heart disease or contagious disease, as well as major psychiatric disorder.
Where this trial is running
Barcelona
- Hospital Universitari Vall d'Hebron — Barcelona, Spain (RECRUITING)
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.
Conditions: Irritable Bowel Syndrome