Healthy Volunteer Recruitment and MRI & MEG Brain Scans for NIMH Studies
This study aims to gather information about your overall health, including mental and physical aspects, through online self-report and in-person assessments, which may involve MRI scans and various psychological, emotional, physiologic, and cognitive tests.
Data Collection
Collected at a single point in time - Cross-sectionalPsychological Well-Being
+ Behavior
+ Personal Satisfaction
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: November 1, 2017
Actual date on which the first participant was enrolled.This study aims to create a list of healthy adult volunteers for research studies at the National Institute of Mental Health (NIMH) in Bethesda, Maryland. It also seeks to develop a set of normal brain MRI scans and MEG recordings linked to healthy volunteer characteristics. The study is important as it aims to maximize the scientific impact of data from volunteers by sharing it broadly with other researchers. The study is open to adult males and females in good health who are 18 to 70 years old. The study consists of two parts. The first part is an online screen where interested participants complete online forms to determine their eligibility for the second part, which is an in-person assessment at the NIH Clinical Center. There are also three optional procedures: an MRI brain scan, MEG recording, and electrocardiography (EKG) done at the NIH Clinical Center. Participants found ineligible due to significant or unstable medical or mental health conditions will be referred back to the community. Those eligible will undergo a clinical assessment that may include safety assessment, vital signs, history and physical, labs, cognitive tests, mental health surveys, and a structured psychiatric diagnostic interview. Some assessments may be conducted virtually. The primary outcome is a list of well-characterized healthy volunteers, while the secondary outcome is the upload of de-identified healthy volunteer characterization data to an open access data repository for secondary research purposes.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.2000 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
National Institutes of Health Clinical Center
Bethesda, United StatesOpen National Institutes of Health Clinical Center in Google Maps