tDCS and Urge in BFRBs

Part of paid clinical trials in Lexington, Kentucky.

Sponsor
Gopalkumar Rakesh
Study ID
NCT07019571
Status
Recruiting

Conditions

  • Repetitive Compulsive Behavior

Eligibility Criteria

Sex
ALL
Age
18 Years - 60 Years
Healthy Volunteers
Not accepted

Interventions

  • Wireless Multichannel Transcranial Current Stimulator (tDCS) — DEVICE
    tDCS will be delivered for 13 minutes (active) or only at the beginning and end of the 13 minute period (sham) using Neuroelectrics Instrument Controller software and a battery-driven Starstim 8-channel transcranial direct current stimulator with 1cm2 ceramic electrodes and SIGNAGEL conductive saline gel.
  • Cue exposure — BEHAVIORAL
    Participants will undergo three, twenty-second trials of exposure to individualized cues at the top of the established urge hierarchy, previously determined to precede picking or biting behaviors before and after tDCS.
  • Boredom induction — BEHAVIORAL
    Participants will be left in the testing room without access to a cellphone or reading materials for 2 different 6 minute periods.

Study Details

The goal of this study is to find out if brain stimulation can help people stop skin-picking or nail-biting. The study wants to answer two main questions: 1. Does brain stimulation reduce the urge to pick skin or bite nails after those urges are triggered? 2. Does brain stimulation reduce how often people pick their skin or bite their nails? Participants will: * Talk about their skin-picking, nail-biting, and other mental health concerns * Be placed in situations that make them want to pick or bite * Rate how strong their urges are before and after brain stimulation Researchers will compare real brain stimulation to a placebo (a fake version that looks the same but has no effect) to see if the real stimulation works to reduce skin-picking and nail-biting urges and behaviors.

Key Dates

Start date
Jul 8, 2025
Status verified
Jul 2025
Primary completion
May 31, 2026
Completion
May 31, 2026

Study Design

Enrollment
55 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: active multifocal Transcranial Direct Current Stimulation (tDCS)
    participants receive 13-min of active multifocal tDCS targeting the left dorsolateral prefrontal cortex. tDCS will be delivered offline for 13 minutes (1.5mA, 10 seconds ramp in/out).
  • Sham Comparator: sham multifocal Transcranial Direct Current Stimulation (tDCS)
    Sham stimulation will be identical to active but electrical current will only be ramped in/out at the beginning and end of the 13-min period.

Primary Outcome Measure

Change in subjective urge [ Time Frame: baseline and post intervention, approximately 90 minutes ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
University of KentuckyLexingtonKentucky40506
Hannah Wild
859-414-6962
Gopalkumar Rakesh, MD (PRINCIPAL_INVESTIGATOR)

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