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Caloric Vestibular Stimulation for Modulation of Insight in Obsessive-Compulsive Spectrum Disorders

Caloric Vestibular Stimulation for Modulation of Insight in Obsessive-Compulsive Spectrum Disorders

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03918577
Enrollment
16
Registered
2019-04-17
Start date
2022-05-10
Completion date
2026-12-30
Last updated
2026-01-22

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

Conditions

Body Dysmorphic Disorders, Illness Anxiety Disorder, Obsessive-Compulsive Disorder

Keywords

Caloric Vestibular Stimulation, Insight

Brief summary

This study investigates whether caloric vestibular stimulation can modulate a measure of insight in obsessive-compulsive spectrum disorders.

Detailed description

Obsessive-compulsive and related disorders (OCRD), including obsessive compulsive disorder and body dysmorphic disorder, are chronic and disabling conditions characterized by recurrent intrusive thoughts and associated compulsive behaviors that affect millions of individuals in the US each year. Individuals affected by OCRD differ in insight, or the degree to which they understand their intrusive thoughts to reflect illness. Impairments in insight limit individuals' motivation to engage in care and predict worse outcome in those who access treatment. This study seeks to explore whether unilateral stimulation of the vestibular system, which activates cortical areas hypothesized to underlie clinical insight, may beneficially modulate insight in individuals with OCRD.

Interventions

Cold water creates a convection current in the semicircular canal of the vestibular apparatus, leading to brief (\<3 min) and typically well tolerated sense of rotational movement. Similar stimulation is routinely used in standard vestibular diagnostic testing.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Intervention model description

randomized, controlled crossover study

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-65 * Primary diagnosis of Obsessive-Compulsive Disorder, Body Dysmorphic Disorder, Illness Anxiety Disorder or Somatic Symptom Disorder (excluding "with predominant pain") * Strongly held OCRD-related concerns meeting BABS score criterion. * No recent change in psychopharmacological treatment, if any * Capacity to provide informed consent

Exclusion criteria

* Psychiatric or medical conditions (eg, vertigo, history of otological surgery) that might make participation unsafe * Pregnant or nursing women * Active or recent substance use

Design outcomes

Primary

MeasureTime frameDescription
change in clinical insight as measured by the Brown Assessment of Beliefs (BABS).1 hourChanges in clinical insight will be rated using the BABS, a gold-standard measure for assessing multiple dimensions of clinical insight across psychiatric disorders. The BABS is a 24 point scale for which scores ≥13 suggest poor or absent insight.

Countries

United States

Contacts

CONTACTPavithra Mukunda, MS
ocdresearch@stanford.edu650-723-4095
CONTACTMaria Filippou-Frye, MD, MBS
ocdresearch@stanford.edu650-723-4095
PRINCIPAL_INVESTIGATORPeter J van Roessel, MD, PhD

Stanford University

Outcome results

None listed

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