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Medical Mindfulness: Virtual Reality Mindfulness Therapy for Eating Disorders

Medical Mindfulness: Virtual Reality Mindfulness Therapy for Anxiety and Pain Management in Adolescent and Young Adult Patients With Eating Disorders

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03745833
Enrollment
30
Registered
2018-11-19
Start date
2019-01-31
Completion date
2019-09-30
Last updated
2018-11-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abdominal Pain, Anxiety, Eating Disorder

Brief summary

Adolescents and young adults with eating disorders undergoing refeeding on an inpatient unit often experience abdominal pain and anxiety either as a result of their medical condition or as an expected side effect of nutritional rehabilitation. The purpose of this study is to assess if VR (Virtual Reality) mindfulness therapy is more or as effective as the standard of care (supportive care such as aromatherapy, heat packs, distraction, and nausea bands) for treating and/or preventing anxiety and pain in patients with eating disorders during the re-nourishment process. The anticipated primary outcome will be reduction of abdominal pain and anxiety with utilization of this intervention.

Detailed description

In this study, investigators hope to 1) assess acceptance of VR mindfulness among inpatient adolescents and young adults with eating disorders 2) assess effects of VR mindfulness on perceived abdominal pain and 3) determine the impact of VR mindfulness on anxiety scores. This study is designed to test the feasibility, acceptability and effectiveness of VR mindfulness in patients as they undergo various medical and nutritional therapies to treat their conditions.

Interventions

Participating patients will be provided with a VR headset (pre-programmed with mindfulness content) after lunch for 15 minutes with supervision while on strict bedrest. The headset will be collected following the intervention. Patients are currently provided with a post-meal survey following all meals as part of the standard of care, and will complete the survey following the lunchtime intervention.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
11 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* patients admitted to the inpatient medical unit for refeeding for malnutrition

Exclusion criteria

* non-English speakers

Design outcomes

Primary

MeasureTime frameDescription
Abdominal pain1 hour after mealsWe will measure pre- and post-intervention pain scores using the validated Faces Pain Scale

Secondary

MeasureTime frameDescription
Anxiety1 hour after mealsWe will measure pre- and post-intervention anxiety scores using the validated Hamilton Anxiety Scale

Contacts

Primary ContactMegen Vo, MD
megenvo@stanford.edu5182218601
Backup ContactColleen Surmay, NP
csurmay@stanfordchildrens.org6509884106

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026