A Pilot Study Using Gut-Directed Hypnotherapy for Hospitalized Patients

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorStanford University

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Gut directed hypnotherapy via telephone intervention

    Behavioral

    Participants will undergo a self-directed gut-directed hypnosis intervention over the telephone.

  • Educational recording

    Behavioral

    Participants will listen to educational material over the telephone about their gastrointestinal symptoms.

Treatment groups

26 Participants
are divided into 2 treatment groups
Group A: HypnosisExperimental treatment 1 intervention
Group B: EducationSham comparator 1 intervention

Trial outcomes

Primary outcomes

1

Recruitment rate

Recruitment rate is the proportion enrolled among eligible patients approached.

Time frame
Up to 1 year.
2

Number of participants who adhered to intervention

Proportion of participants completing ≥1 hypnosis session during hospitalization and total number of listens

Time frame
3 months.
3

Retention rate

Retention rate is defined as survey completion at baseline, 1 week, 1 month, and 3 months.

Time frame
3 months.

Secondary outcomes

Other outcomes

Sponsors and contacts

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Stanford University

Lead sponsor

American College of Gastroenterology

Collaborator

This trial is not recruiting at the moment. You can still explore other options: