About this trial

The purpose of the study is to compare the effectiveness of recorded gut-directed hypnosis to an educational recording in people with chronic problems in their gastrointestinal (GI) system. Patients who are hospitalized at Stanford Hospital for worsening pain and/or nausea will be considered for enrollment.

Eligibility criteria

Qualifiers

Adults admitted to the GI inpatient service with expected length of stay >24 hours

Prior diagnosis of a disorder of gut-brain interaction, esophageal disorder, or inflammatory bowel disease

Reason for hospitalization related to symptom management for exacerbation of visceral pain and/or nausea.

Disqualifiers

Currently using hypnosis

severe developmental delay or cognitive impairment

serious mental illness (i.e. psychosis or dissociation)

hearing impairment

Trial design

Treatments tested in this trial

  • Gut directed hypnotherapy via telephone intervention
  • Educational recording

Treatment groups

26 Participants
are divided into 2 treatment groups

Locations

1
Stanford University94305, StanfordCalifornia, United States

Sponsors and collaborators

Stanford University

Lead sponsor

American College of Gastroenterology

Collaborator