RecruitingNCT06073886
Personalized brain stimulation for lasting symptoms after concussion
About this title
Read the official source — NCT06073886Device studyAges 18–65United StatesPTSD
Understand this study
Who could participate?
Listed age limits: 18 years to 65 years.
- Listed locations
- Westwood, Los AngelesSee all locations and recruitment
- Study phase
- Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
What to know before participating
A point to clarify
This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?
Things to check before joining
Study start dateStarted: March 6, 2024
- Recruitment status
- Recruiting
- Enrollment listed in the registry
- 75
- Sponsor
- University of California, Los Angeles
- Sponsor type
- University
- Study type
- Behavioral
- Intervention type
- Behavioural, Device
- Study phase
- Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
- Locations
- United States
- Age range
- From 18 Years to 65 Years
- Official registry ID
- NCT06073886
- Official title
Show the full official title
Personalized Circuit-Based Frontoamygdala Neuromodulation for Persistent Post-Concussive Symptoms
Recruitment & locations
Currently recruitingA study may be recruiting, but some locations may no longer be accepting participants. Confirm availability with the research team.
Westwood, Los Angeles
Interested in joining this study?
Questions about this study
Who is behind this study?
The study sponsor is University of California, Los Angeles, a university.
Who can participate?
Listed age limits: 18 years to 65 years.
Is this study still recruiting?
The registry lists this study as recruiting.
