Skip to main content
Clinical Trials/ACTRN12622000429752
ACTRN12622000429752
Not yet recruiting
Phase 2

The effect of using oxytocin in individuals with body dysmorphic disorder (BDD)

Swinburne University of Technology0 sites46 target enrollmentMarch 16, 2022

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Body Dysmorphic Disorder
Sponsor
Swinburne University of Technology
Enrollment
46
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 16, 2022
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Participants will i) be aged between 18\-55 years (inclusive); ii) have a primary diagnosis of BDD according to the Diagnostic and Statistical Manual\-5 (DSM\-5\); iii) score of 24 or higher on the BDD\-YBOCS (to ensure at least moderate symptom severity); iv) have an estimated IQ of 70 or higher as assessed using the Test of Premorbid Functioning (TOPF) to ensure no intellectual disability and study instructions are understood; v) have been stabilised on psychotropic medications, if prescribed, for 8weeks or longer; vi) be right\-handed (to meet eligibility for MRI); vii) utilising effective contraception if female and of childbearing age; and viii) have capacity to consent to the study. Further, BDD patients frequently report co\-morbid depression, social anxiety and psychoses. To ensure our sample is representative, patients with co\-morbidities will be included.

Exclusion Criteria

  • Participants will be excluded if i) substance use disorder is present; ii) they are unable to meaningfully converse in, or read, English; iii) they have metal implants or a history of claustrophobia (to meet eligibility for an MRI); iv) neuroendocrine dysfunction or steroid use is present; vi) they have been diagnosed with any known neurological disorder; v) they are currently pregnant or breastfeeding, vi) have an ongoing sinus condition and vii) history of hypersensitivity to oxytocin.

Outcomes

Primary Outcomes

Not specified

Similar Trials