JHU COACH

Center for OCD, Anxiety, and Related Disorders for Children

Leveraging Technological Advancements to Improve the Treatment of Trichotillomania

New technologies are one possible solution to help identify and reduce pulling behaviors associated with trichotillomania (TTM). The Keen 2 is one such technology, which is a bracelet which gives the user alerts in the form of a vibration when the user is engaging in hair pulling behavior. Thus, using the Keen 2 could positively increase the awareness of pulling behaviors. This project will examine the effects of using the Keen 2 on hair pulling and related psychiatric symptoms in individuals with trichotillomania. (IRB00279950)

Funding Source: COACH Gift Fund (made possible by generous donations from patients, participants, and families who have received care through our program)

To be eligible to participate, you must:

  • be 18 years of age or older 
  • be an English speaker 
  • engage in hair pulling behaviors 
  • be able to attend three in-person study visits at COACH 
  • be comfortable wearing a wrist-worn device for four weeks 

Overview of Study Procedures

Phone Screen

The phone screen will allow us to learn more about you to help us determine if the study will be a good fit. The initial intake phone call may take up to 30 minutes.

Visit 1

At the initial visit, you will complete an interview and some questionnaires to determine if you are a good fit for the study. If you are a fit, you will receive instructions on how to properly use and wear the Keen2 device.  

Visit 2

At the second visit, you will be re-administered questionnaires, complete a computer task, and transfer Keen app data from your phone to a secure lab computer.

Visit 3

At the third visit, you will be re-administered the questionnaires, complete a computer task, and complete the transfer of Keen in-app data.  

Interested? Participate in Our Research!

Participate

Study Team Members

FAQs

Can I still participate without a condition?

Yes! Even if you do not have a psychiatric condition, you can still help us learn more about how best help patients and families overcome them. Scientific research often required what is a called a “control group.” In our research, data that “control” participants contribute help us understand a specific condition better. Participants are compensated for their time!

What is done with my information if I participate?

Any information you share with us will NOT be provided to anyone (including your insurance/ health care provider) without you formally submitting a written request that we do so. We strictly follow the data collection and storage policy as outlined by The Johns Hopkins University School of Medicine in order to protect your privacy and the confidentiality of the information you provide.

Will I be compensated for my participation?

Yes! Participants receive compensation in the form of gift cards, the value of which is determined by the study they complete.

How do I get in touch with the study team?

Contact our research coordinator by email (coach@jhmi.edu) or by phone (443-300-8836) indicating that you are interested in participating. If you are under the age of 18, please have a parent or legal guardian contact us on your behalf.