Open Studies Enrolling Participants
Together with the Carolina Center for Neurostimulation, we are actively recruiting participants for several clinical trials.
Why participate? We find that people decide to participate in clinical trials because they are looking for a new and different approach to managing their mental health. Also, people often participate because they are motivated to help with the discovery and development of new treatments for their condition. If you have general questions about our clinical trials, we welcome you to contact us. We look forward to hearing from you!
Why participate? We find that people decide to participate in clinical trials because they are looking for a new and different approach to managing their mental health. Also, people often participate because they are motivated to help with the discovery and development of new treatments for their condition. If you have general questions about our clinical trials, we welcome you to contact us. We look forward to hearing from you!
Studies Looking for Participants with Anxiety
At-Home Cranial Electrotherapy Stimulation (CES) for the Treatment of Generalized Anxiety Disorder in Young Adults: Double-Blind Sham-Controlled Randomized Clinical Trail
Study Purpose:
Investigate the efficacy of an at-home brain stimulation device for the treatment of Generalized Anxiety Disorder in young adults.
Target Population:
Young adults (18-21) diagnosed with Generalized Anxiety Disorder.
Compensation:
Up to $500.
Participants may qualify if they:
Study Procedures:
Interested?
Find out if you are eligible with our brief and secure online screening survey: bit.ly/cesgad_fl
Have Questions?
Please email [email protected] with any questions and a member of our research team will reach back out!
IRB #22-3341: If you have questions or concerns about your rights as a research subject you may contact the UNC Institutional Review Board at contact [email protected].
Investigate the efficacy of an at-home brain stimulation device for the treatment of Generalized Anxiety Disorder in young adults.
Target Population:
Young adults (18-21) diagnosed with Generalized Anxiety Disorder.
Compensation:
Up to $500.
Participants may qualify if they:
- Are between the ages of 18 and 21 years old
- Regularly experiencing anxiety symptoms
- Are not diagnosed with psychosis, bipolar disorder, epilepsy, or substance-use disorder
Study Procedures:
- Remote screening interview
- Two in-person visits
- 6 weeks of daily at-home brain stimulation with questionnaires and weekly check-ins
- 5 weeks of online follow-up questionnaires
- Final phone interview
Interested?
Find out if you are eligible with our brief and secure online screening survey: bit.ly/cesgad_fl
Have Questions?
Please email [email protected] with any questions and a member of our research team will reach back out!
IRB #22-3341: If you have questions or concerns about your rights as a research subject you may contact the UNC Institutional Review Board at contact [email protected].
Studies Looking for Participants with Depression Symptoms
Treatment trial for Major Depressive Disorder using non-invasive brain stimulation
Study Purpose:
The purpose of this study is to investigate whether five days of personalized non-invasive brain stimulation can improve depression in people aged 18-70 who have been diagnosed with major depressive disorder.
Target Population:
Adults diagnosed with Major Depressive Disorder with current depressive symptoms.
Time Commitment:
Filling out a prescreening questionnaire (about 3-5 minutes), 1x virtual screening session (about 45 minutes-1hr), an optional MRI session (15 min MRI; 1 hr total session), 5x in-person stimulation sessions (Monday to Friday, about 3.5 hrs on Mon and Fri and 1.5 hours on Tue-Thu, scheduled flexibly; includes high density electroencephalography (HD-EEG) on Monday and Friday), and 1x in person follow-up session two weeks later (approximately 1.5 hours, including HD-EEG). Total participation time is about 14 hours over 3 weeks.
Compensation:
Up to $430 upon completion of the in-person session.
Participants may qualify if they:
Interested?
You can check your eligibility with our brief and secure online screening tool: https://bit.ly/CLACS-CW
Questions:
For any questions please contact the research team at CLACS-RCT@med.unc.edu
IRB: #24-2166
If you have questions or concerns about your rights as a research subject, you may contact the Sterling Institutional Review Board Regulatory Department at telephone number 1-888-636-1062 (toll free) or [email protected].
The purpose of this study is to investigate whether five days of personalized non-invasive brain stimulation can improve depression in people aged 18-70 who have been diagnosed with major depressive disorder.
Target Population:
Adults diagnosed with Major Depressive Disorder with current depressive symptoms.
Time Commitment:
Filling out a prescreening questionnaire (about 3-5 minutes), 1x virtual screening session (about 45 minutes-1hr), an optional MRI session (15 min MRI; 1 hr total session), 5x in-person stimulation sessions (Monday to Friday, about 3.5 hrs on Mon and Fri and 1.5 hours on Tue-Thu, scheduled flexibly; includes high density electroencephalography (HD-EEG) on Monday and Friday), and 1x in person follow-up session two weeks later (approximately 1.5 hours, including HD-EEG). Total participation time is about 14 hours over 3 weeks.
Compensation:
Up to $430 upon completion of the in-person session.
Participants may qualify if they:
- Are between the ages of 18-70 years
- Have a diagnosis of Major Depressive Disorder
- Have NOT been diagnosed with Bipolar Disorder, a Psychotic Disorder, Schizophrenia or Autism
Interested?
You can check your eligibility with our brief and secure online screening tool: https://bit.ly/CLACS-CW
Questions:
For any questions please contact the research team at CLACS-RCT@med.unc.edu
IRB: #24-2166
If you have questions or concerns about your rights as a research subject, you may contact the Sterling Institutional Review Board Regulatory Department at telephone number 1-888-636-1062 (toll free) or [email protected].
Inter-brain Synchronization of the Therapist-Client Dyad in Psychotherapy: Pilot EEG Study in Students with Mild-Moderate Depression Symptoms
We are very excited to announce that we are now recruiting for a new research study on brain activity in client and therapist during psychosocial interventions. We are looking for full-time students between age 18 and 30 who experience depression symptoms.
Eligible participants will have a session of brain activity recording using electrodes on the scalp while participating in a single session of psychosocial intervention: Behavioral Activation or Psychoeducation. If you are interested in learning more about the research study, we encourage you to check out Research for Me at UNC where you can sign up to get screened.
You can always also reach out to us by email at [email protected] with questions about participation. The research study includes 1 phone screen, online questionnaires, and 1 study visit at the Carolina Center for Neurostimulation (100 Market Street Chapel Hill, NC 27514)
Total time commitment of your participation is expected to be up to 5 hours. Participants will be compensated up to $65 for participation.
This study has been approved by the UNC IRB#: 22-1422, P.I: Flavio Frohlich, PhD.
For IRB-related questions, please contact [email protected].
Eligible participants will have a session of brain activity recording using electrodes on the scalp while participating in a single session of psychosocial intervention: Behavioral Activation or Psychoeducation. If you are interested in learning more about the research study, we encourage you to check out Research for Me at UNC where you can sign up to get screened.
You can always also reach out to us by email at [email protected] with questions about participation. The research study includes 1 phone screen, online questionnaires, and 1 study visit at the Carolina Center for Neurostimulation (100 Market Street Chapel Hill, NC 27514)
Total time commitment of your participation is expected to be up to 5 hours. Participants will be compensated up to $65 for participation.
This study has been approved by the UNC IRB#: 22-1422, P.I: Flavio Frohlich, PhD.
For IRB-related questions, please contact [email protected].