Overview

Behavioral Treatment and Memantine in Body Focused Repetitive Behaviors

Status:
Not yet recruiting
Trial end date:
2024-06-01
Target enrollment:
0
Participant gender:
All
Summary
The goal of the proposed study is to compare the efficacy of behavioral treatment (BT) to memantine, a psychopharmacological agent, for BFRBs. 28 subjects with trichotillomania (TTM) or skin picking disorder (SPD) will receive 8 weeks of memantine treatment, followed by 8 weeks of comprehensive behavioral therapy (ComB) treatment. The hypothesis to be tested is that behavioral therapy will be associated with superior clinical outcomes as compared to memantine. A second hypothesis is that both memantine and behavioral therapy will demonstrate improvement from baseline to the respective posttreatment assessment.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Chicago
Treatments:
Memantine
Criteria
Inclusion Criteria:

- Men and women ages 18+

- Current DSM-5 diagnosis of trichotillomania (TTM) or skin picking disorder (SPD)

- Ability to understand and sign the consent form

- Stable dose of medications for at least the past 3 months

Exclusion Criteria:

- Unstable medical illness based on history or clinically significant abnormalities on
baseline physical examination

- Current pregnancy or lactation, or inadequate contraception in women of childbearing
potential

- Subjects considered an immediate suicide risk based on the Columbia Suicide Severity
rating Scale (C-SSRS)

- Past 12-month DSM-5 diagnosis of psychosis, bipolar disorder, mania, or a substance or
alcohol use disorder

- Illegal substance use based on urine toxicology screening

- Previous treatment with memantine

- Previous trial of ComB or similar BT protocol (e,g., habit reversal training)

- Cognitive impairment that interferes with the capacity to understand and
self-administer medication or provide written informed consent