Clinical trial Recruiting at 1 site Interventional Ages 18 to 95

Using a vibrating bracelet to help stop nail biting

Official title: Habit Awareness Device for Treatment of Onychophagia

Run by Weill Medical College of Cornell University · NCT06111729 · Data updated 2026-11-12

This study is testing whether a vibrating bracelet can help adults who bite their nails stop the habit and improve their quality of life.

Quick facts

Study typeInterventional
Ages18 Years to 95 Years
SexAll
Enrollment10 (estimated)
SponsorWeill Medical College of Cornell University
Academic / other
Locations1 site (New York, New York)
StatusRecruiting
StartedJanuary 24, 2023
Main results expectedMay 2027
Study endsMay 2027
Registry record updatedApril 21, 2026
Trial IDNCT06111729 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18-95 who have been diagnosed with onychophagia.

Probably not a fit

Patients who are pregnant, planning to become pregnant, or nursing may not receive benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial investigates the effectiveness of a vibrating bracelet designed to reduce nail-biting behavior in adults diagnosed with onychophagia. Participants will wear the bracelet for 12 weeks, which vibrates gently whenever it detects nail-biting, prompting users to become more aware of their habit. An accompanying app will track the frequency of vibrations and monitor changes in nail-biting behavior over the study period. The goal is to determine if this device can significantly decrease the incidence of nail biting and improve participants' quality of life.

Why it matters

Potential benefit: If successful, this intervention could provide a non-invasive method for individuals to reduce nail-biting and its associated negative impacts.

How similar studies have gone: While the specific use of a vibrating bracelet for nail-biting is novel, similar behavioral interventions have shown promise in other contexts.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Patients diagnosed with onychophagia
2. Must understand and voluntarily sign an informed consent form
3. Must be aged 18-95 years at the time of consent
4. Must be able to adhere to the study visit schedule and other protocol requirements

Exclusion Criteria:

1. Subject is unable to provide written informed consent for any reason.
2. Subject is sensitive or allergic to any of the elements included in this study.
3. Subject is unable to complete the required pain dairy.
4. Subject is pregnant, planning pregnancy, or nursing.
5. Subject does not have a compatible personal device with either IOS 13.0 or greater or Android version 6.0 or greater.

Where it's running

  • Weill Cornell Department of Dermatology
    New York, New York, United States
    Recruiting

Study contacts

  • Principal investigator: Shari Lipner, MD, PhD — Professor of Clinical Dermatology
  • Study coordinator: Eden Axler, BS
  • Email: eda4007@med.cornell.edu
  • Phone: 6469623376

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

  • Iron treatment for children and young adults with Crohn’s disease and iron deficiency anemia

    This study tests how different iron treatment approaches work for kids and young adults with Crohn’s disease and iron deficiency anemia.

    Recruiting Phase 4 Weill Medical College of Cornell University · New York, New York · NCT07925450

  • App-assisted Medical Nutrition Therapy for diabetes with insulin use

    This study tests whether using the Undermyfork Care app together with nutrition counseling improves blood sugar, cholesterol, quality of life, activity, and eating choices in adults with type 1 or type 2 diabetes who use insulin.

    Recruiting Weill Medical College of Cornell University · New York, New York · NCT07773779

  • Autologous Fat Grafting for Chronic Tendinopathy

    This study tests whether a person’s own processed fat injected into a painful tendon can reduce pain and improve function in adults with chronic tendinopathy who have not improved with standard treatments.

    Recruiting Weill Medical College of Cornell University · New York, New York · NCT07748793

  • Digital mindfulness app for teens with eczema

    Teens with moderate to severe eczema try a digital mindfulness app to see if it helps control symptoms and improve quality of life.

    Recruiting at 2 sites Weill Medical College of Cornell University · New York, New York and 1 other locations · NCT07746427

  • Low-Dose TBI Plus CAR-T Therapy for relapsed/refractory DLBCL or multiple myeloma

    This trial tests whether giving a single low dose of total body irradiation before CAR-T therapy is safe and helps the treatment work better for adults with relapsed or refractory DLBCL or multiple myeloma.

    Recruiting Phase 1 Weill Medical College of Cornell University · New York, New York · NCT07725406

  • Lowering gas pressure in robotic surgery to reduce pain after surgery

    In adults undergoing robot-assisted surgery, this study tests whether using low-pressure CO2 with the AirSeal device reduces pain and speeds recovery compared with standard-pressure gas.

    Recruiting Weill Medical College of Cornell University · New York, New York · NCT07710352

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.