Skip to content

tDCS and Urge in BFRBs

Evaluating the Impact of Transcranial Direct Current Stimulation on Urge in Body-Focused Repetitive Behaviors

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07019571
Enrollment
55
Registered
2025-06-13
Start date
2025-07-08
Completion date
2026-05-31
Last updated
2025-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Repetitive Compulsive Behavior

Keywords

picking, biting, transcranial stimulation

Brief summary

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.

Interventions

DEVICEWireless Multichannel Transcranial Current Stimulator (tDCS)

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.

BEHAVIORALCue exposure

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.

BEHAVIORALBoredom induction

Participants will be left in the testing room without access to a cellphone or reading materials for 2 different 6 minute periods.

Sponsors

Gopalkumar Rakesh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Ability to provide informed consent (as established by clinical interview), and voluntary, signed informed consent prior to the performance of any study specific * Ability and willingness to perform study-relevant clinical assessments and tDCS * Endorses mild to extreme intensity of urges to pick or bite their skin or nails

Exclusion criteria

* Any unstable medical, psychiatric, or neurological condition (including active or otherwise problematic suicidality) that may necessitate urgent treatment * Daily use of psychotropic medications that substantially lower seizure threshold (e.g., clozapine) * History of psychosis, mania, major neurological disorder, significant head trauma, or seizures/epilepsy * Current suicidal intent * Any major neurological disease or history of major head trauma, including concussion with extended loss of consciousness, or of psychosurgery * Current or suspected pregnancy * Endorsing possible contraindications for tDCS

Design outcomes

Primary

MeasureTime frameDescription
Change in subjective distressbaseline and post intervention, approximately 90 minutesIndividuals will rate their distress using a scale (1-10) with a higher score meaning greater distress. They will rate their distress three times in a row, at two different time-points.
Change in subjective urgebaseline and post intervention, approximately 90 minutesIndividuals will rate their urge to pick using a scale (1-10) with a higher score meaning greater urge. They will rate their urge three times in a row, at two different time-points.
Change in picking or biting behavioral frequencybaseline and post intervention (approximately 90 minutes)Picking or biting behaviors will be assessed via two 6-minute blocks of visual observation, before and after tDCS. The frequency of the behaviors observed will be collected in each block. Change in total frequency between blocks will be calculated.
Change in picking or biting behaviors durationbaseline and post intervention (approximately 90 minutes)Picking or biting behaviors will be assessed via two 6-minute blocks of visual observation, before and after tDCS. Duration of the behaviors observed will be collected in each block. Change in total duration between blocks will be calculated.

Countries

United States

Contacts

Primary ContactHannah Wild, M.S.
hannah.wild@uky.edu‪(859) 414-6962‬

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026