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) — DEVICEtDCS 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 — BEHAVIORALParticipants 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 — BEHAVIORALParticipants 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
- Hannah Wild, M.S.(859) 414-6962
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Kentucky | Lexington | Kentucky | 40506 | Gopalkumar Rakesh, MD (PRINCIPAL_INVESTIGATOR) |