Recruiting

Healthy Volunteer Recruitment and MRI & MEG Brain Scans for NIMH Studies

0 criteria met from your profileSee at a glance how your profile meets each eligibility criteria.
Study Aim

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.

What is being collected

Data Collection

Collected at a single point in time - Cross-sectional
Who is being recruted

Psychological Well-Being

+ Behavior

+ Personal Satisfaction

From 18 to 70 Years
+16 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: November 2017
See protocol details

Summary

Principal SponsorNational Institute of Mental Health (NIMH)
Study ContactCarlos A Zarate, M.D.
Last updated: March 25, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleRecruitment and Characterization of Healthy Research Volunteers for NIMH Intramural Studies
NCT03304665
Principal SponsorNational Institute of Mental Health (NIMH)
Study ContactCarlos A Zarate, M.D.
Last updated: March 25, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

2000 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Psychological Well-BeingBehaviorPersonal Satisfaction

Criteria

4 inclusion criteria required to participate
18 - 70 years of age

Able to read, speak, and understand English

Able to provide informed consent

In current good general health

12 exclusion criteria prevent from participating
Metal in body which would make having an MRI scan unsafe

Being uncomfortable in small, closed spaces such as the MRI machine

Inability to lie comfortably on back for at least 45 minutes

Pregnancy

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

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

Recruiting

National Institutes of Health Clinical Center

Bethesda, United StatesOpen National Institutes of Health Clinical Center in Google Maps
Recruiting
One Study Center