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Evaluation of Patients With Mood and Anxiety Disorders and Healthy Volunteers

StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

The 50 most recent of 367 record versions are accounted for below. See every version on ClinicalTrials.gov ↗

  1. Minor Re-verified, no change to tracked fields
  2. Minor Eligibility criteria expanded, about 3 words
  3. Minor 15 versions Re-verified since Apr 3, 2026, no change to tracked fieldsv351-v365
  4. Minor Eligibility criteria shortened, about 104 wordsv350 Show moreShow less
  5. Minor 15 versions Re-verified since May 30, 2025, no change to tracked fieldsv335-v349
Show 17 earlier versionsHide 17 earlier versions
  1. Minor Study Status, Eligibilityv334
  2. Minor 12 versions Re-verified since Jan 24, 2025, no change to tracked fieldsv322-v333
  3. Minor Study Status, Contacts/Locationsv321
  4. Minor 3 versions Re-verified since Nov 7, 2024, no change to tracked fieldsv318-v320
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this protocol is to allow for the careful screening of patients and healthy volunteers for participation in research protocols in the Experimental Therapeutics and Pathophysiology Lab (ETPB) at the National Institute of Mental Health (NIMH) and for the collection of natural history data. In addition the protocol will allow clinicians to gain more experience in the use of a variety of polysomnographic and high-density EEG recordings. Subjects in this protocol will undergo an evaluation which may include: a psychiatric interview; a diagnostic interview; rating scales; a medical history; a physical exam; brain magnetic resonance imaging (MRI); electroencephalography (EEG); electrocardiography (EKG), magnetoencephalography (MEG); blood, saliva and urine laboratory evaluation; and a request for medical records. Subjects may also be asked to complete questionnaires about attitudes towards research and motivation for research participation. The data collected may also be linked with data from other mood and anxiety disorder protocols (e.g., brain imaging, DNA, psychophysiology tests, treatment studies, etc) for the purposes of better understanding the diagnosis, pathophysiology, and treatment response of patients with mood disorders. Parents of minors will be interviewed. Upon conclusion of the screening process, subjects will either be offered participation in a research protocol and will sign the appropriate informed consent, or will be considered not appropriate for participation in research and will be referred back into the community. The current protocol thus serves as an entry point for individuals with mood or anxiety disorders or healthy volunteers to enter NIMH IRB approved ETPB protocols.
Trial Details
NCT Number NCT00024635
Lead Sponsor National Institute of Mental Health (NIMH)
Collaborators: Suburban Hospital
Conditions Mood Disorders, Anxiety Disorders, Healthy Volunteers, Bipolar Disorder, Depression
Enrollment 16,000 participants
Start Date
Updated on ClinicalTrials.gov