taVNS on the Inpatient Psychiatric Unit

Status Recruiting

Clinical Trial Summary

This is a research study to find out if mental health symptoms in patients admitted to the Institute of Psychiatry are affected by a form of ear stimulation called transcutaneous auricular vagus nerve stimulation, or taVNS. Participants will receive ear stimulation during their inpatient treatment at the Institute of Psychiatry. Participants will be randomly assigned to either receive ear stimulation for 1 day (up to 9 treatments over the course of a single day) or 3 days (up to 3 treatments per day), and will have a 50:50 chance of being in either group (like the flip of a coin). Each treatment will last up to 30 minutes and there will be a break of at least 30 minutes in between treatments. The study team will ask participants to complete a group of questionnaires at the beginning and end of the study. In addition, there are several questionnaires that will be completed daily while participants are receiving ear stimulation. Participants in the 1 day stimulation group will also receive 2 days of follow up questionnaires after the initial day of stimulation. The questionnaires will ask questions about mental health symptoms that subjects may or may not be experiencing, including questions about mood, anxiety, and sleep. The ear stimulation treatments will not interfere with the care subjects are receiving from the medical team. In order to qualify for this study, participants must be actively receiving inpatient care at the MUSC Institute of Psychiatry.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05791383
Study type	Interventional
Source	Medical University of South Carolina
Contact	Bashar W Badran, PhD
Phone	843-792-6076
Email	badran@musc.edu
Status	Recruiting
Phase	N/A
Start date	December 1, 2022
Completion date	December 2024

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT04122482` - An Online Course for Improving Knowledge and Access to Mental Health Accommodations in Canadian Enterprises	N/A
Completed	`NCT04085861` - Mental Health in Dancers; an Intervention Study	N/A
Recruiting	`NCT06060210` - Impact of Ketamine On Depressive Symptoms In Patients Undergoing Lumbo-peritoneal Shunt Insertion	Phase 4
Active, not recruiting	`NCT04588883` - Strengthening Families Living With HIV in Kenya	N/A
Recruiting	`NCT06065787` - NeuroGlove Anxiety and Depression Study	N/A
Active, not recruiting	`NCT04583891` - Mobile Apps to Reduce Distress in Breast Cancer Survivors Using an Adaptive Design	N/A
Completed	`NCT05554042` - Kintsugi Voice Device Study
Not yet recruiting	`NCT06430853` - Psychobiological Interventions in Pregnancy	N/A
Not yet recruiting	`NCT06162624` - Pilot Effectiveness Trial of an ACT Self-help Workbook Tailored Specifically for Prisons	N/A
Completed	`NCT02954250` - Mindfulness Based Cognitive Therapy for Depression and Cognitive Inhibition in Suicide	Early Phase 1
Recruiting	`NCT05647499` - Evaluating the Back 2 School Program in a Norwegian Setting: A Multicenter Pilot Study	N/A
Completed	`NCT03980873` - Cognitive-Behavioral Therapy for Young Adult Lesbian, Gay and Bisexual: Transdiagnostic Minority Stress Approach	N/A
Completed	`NCT04422327` - The Impact of a Combination of Bifidobacterium Longum 35624® and 1714™ Strains in Adults With Irritable Bowel Syndrome	Phase 1/Phase 2
Completed	`NCT05368155` - Chronic Pelvic Pain and Education Skills Training for Women Veterans	N/A
Completed	`NCT05455905` - Voice Biomarkers Predictive of Depression and Anxiety
Completed	`NCT03272516` - Mindfulness Based Cognitive Therapy (MBCT) for Primary Care Patients	N/A
Not yet recruiting	`NCT06027047` - Breakthrough Anxiety and Sleep Evaluation Using Linked Devices and Smartphone Application Onar (BASEL)
Not yet recruiting	`NCT05535101` - Non-invasive Brain Stimulation in Patients With Methamphetamine Use Disorder	N/A
Recruiting	`NCT04418115` - Fatigue as a Late Effect in Breast Cancer Survivors - is Acupuncture a Treatment Option?	N/A
Completed	`NCT04905524` - Activity Changes in Irritable Bowel Syndrome (IBS), Anxiety, and Depression Following the Use of Viome Precision Nutrition Program (VPNP)	N/A