Behavioral Treatment and Memantine in Body Focused Repetitive Behaviors

Sponsor
University of Chicago (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05796752
Collaborator
(none)
28
1
12

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Detailed Description

Hair pulling disorder (i.e., trichotillomania, TTM) and skin picking disorder (SPD) are often categorized under the umbrella term of BFRB disorders. These repetitive, intentionally performed behaviors often cause noticeable cosmetic issues and may result in clinically significant distress or functional impairment.

Behavioral therapy (BT) is generally regarded as the first-line treatment for BFRBs. One type of BT is comprehensive behavioral treatment (ComB), a treatment that emphasizes habit reversal training and various techniques that target specific BFRB triggers (e.g., sensory cues, such as pressure on the scalp; environmental cues, such as bright lights and mirrors), including emotion dysregulation. The ComB protocol was methodically developed based on expert consensus and demonstrated promising results in one single case design study and a randomized controlled trial comparing it to a minimal attention control condition.

Research has also found benefit of pharmacological agents in the treatment of BFRBs. Most recently, a randomized controlled trial of memantine vs. placebo found statistically significant improvements in disorder severity and life functioning in the memantine group as compared to the placebo group.

Although there are emerging behavioral and psychopharmacological interventions for BFRBs, the research is limited. Additionally, there are no studies comparing the efficacy of first-line behavioral treatments to promising medication interventions for this class of disorders. Given the serious personal consequences associated with trichotillomania and skin picking disorder, there is substantial need for additional research to clarify the best available treatments for BFRBs. Doing so would facilitate future research and the development of refined treatment guidelines. Therefore, the current trial aims to compare the efficacy of behavioral therapy and memantine in adults with trichotillomania and skin picking disorder.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
28 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Single-Group Crossover Trial Comparing Behavioral Treatment to Memantine in Body Focused Repetitive Behaviors
Anticipated Study Start Date :
Jun 1, 2023
Anticipated Primary Completion Date :
Jun 1, 2024
Anticipated Study Completion Date :
Jun 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Memantine and Behavioral Therapy

All subjects will receive 8-weeks of memantine treatment (10mg po qday for the first two weeks, then 20 mg po qday for the remaining six weeks). After the 8-weeks of memantine treatment, the dose will be discontinued. Then, after a 4-week washout period, all subjects will receive 8-weeks of ComB therapy. Therapy will be once a week for 30 minutes. After the 8-weeks of ComB treatment, the therapy will be discontinued.

Drug: Memantine
Cognition-enhancing medication
Other Names:
  • Namenda
  • Behavioral: ComB Behavioral Therapy
    Therapy for BFRBs

    Outcome Measures

    Primary Outcome Measures

    1. NIMH Symptom Severity Scale (for TTM or Skin Picking) [The primary efficacy endpoints will be the change in these measures from baseline to week 8 in memantine treatment vs. ComB treatment.]

      The primary efficacy measure will be the change in hair pulling or skin picking frequency and urges to pull hair or pick skin for the past week as indicated by change in total score on the NIMH Symptom Severity Scale (for TTM or Skin Picking. The primary endpoints will be used to examine differential improvements for memantine vs. BT.

    Secondary Outcome Measures

    1. Clinical Global Impressions -- Improvement Scale (CGI-I) [20 weeks]

      A clinician-rated measure to assess global improvement in symptoms. The scale ranges from 1 (Very much improved) to 7 (Very much worse). The results will be dichotomized as improved (CGI-I score of 1 or 2) or not improved (CGI-I score of 3-7). The scale will be assessed at the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    2. Massachusetts General Hospital Hairpulling Scale [20 weeks]

      Brief, self-report instrument for assessing repetitive hairpulling. Seven individual items, rated for severity from 0 to 4, assess urges to pull, actual pulling, perceived control, and associated distress. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    3. Massachusetts General Hospital Hairpulling Scale -- Revised for Skin Picking [20 weeks]

      Brief, self-report instrument for assessing repetitive skin picking. Seven individual items, rated for severity from 0 to 4, assess urges to pick, actual picking, perceived control, and associated distress. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    4. Quality of Life Inventory [20 weeks]

      A self-report assessment of patient perceived quality of life. Higher scores indicate a higher quality of life, whereas lower scores indicate a lower quality of life. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    5. Sheehan Disability Scale (SDS) [20 weeks]

      A self-report measure of functional impairment from TTM or SPD. Higher scores indicate more debilitating TTM or SPD. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    6. Hamilton Anxiety Rating Scale (HAM-A) [20 weeks]

      A clinician-administered assessment of anxiety. Higher scores indicate higher levels of anxiety, with 0 being no symptoms of anxiety. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    7. Hamilton Depression Rating Scale (HAM-D) [20 weeks]

      A clinician-administered assessment of depression. Higher scores indicate higher levels of depression, with 0 being no symptoms of depression. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    8. Barratt Impulsiveness Scale (BIS) [20 weeks]

      A self-report assessment of impulsivity. Higher total scores indicate higher impulsiveness. The scale will be administered at screening, the end of the memantine treatment, at the end of the washout period, and at the end of the ComB therapy treatment.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    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

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • University of Chicago

    Investigators

    • Principal Investigator: Jon E Grant, MD, JD, MPH, University of Chicago
    • Principal Investigator: Gregory Chasson, PhD, University of Chicago

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of Chicago
    ClinicalTrials.gov Identifier:
    NCT05796752
    Other Study ID Numbers:
    • IRB23-0033
    First Posted:
    Apr 3, 2023
    Last Update Posted:
    Apr 3, 2023
    Last Verified:
    Mar 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 3, 2023