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Protocol Details

The Evaluation of Patients with Mood and Anxiety Disorders and Healthy Volunteers

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

01-M-0254

Sponsoring Institute

National Institute of Mental Health (NIMH)

Recruitment Detail

Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 3 Years
Max Age: 99 Years

Referral Letter Required

No

Population Exclusion(s)

Adults who are or may become unable to consent;
Pregnant Women

Keywords

Screening;
Anxiety;
Mood;
Diagnostic Testing;
Natural History

Recruitment Keyword(s)

None

Condition(s)

Mood Disorders;
Anxiety Disorders;
Healthy Volunteers;
Bipolar Disorder;
Depression

Investigational Drug(s)

None

Investigational Device(s)

None

Intervention(s)

None

Supporting Site

National Institute of Mental HealthSuburban Hospital

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.

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Eligibility

INCLUSION CRITERIA:

-Subjects ages 3 to 99 may enroll in the protocol.

-Subjects must be competent to comprehend the purpose of the screening process and to provide written informed consent and be willing to participate in NIMH IRB approved research protocols. Minors will be asked to assent and their parents will sign the consent form.

-Subjects will undergo an evaluation which may include a psychiatric interview, medical (including Tanner staging for minors), neurological, and laboratory examinations (as appropriate such as EKG, EEG, renal and liver function tests, serum electrolytes, urinalysis, HIV, hepatitis A, B, and C, lupus anticoagulant, anticardiolipin (aCL) antibodies, anti-b2glycoprotein-I antibodies, PT/PTT, blood levels of psychotropic drugs, pregnancy testing, and urine drug screen for the presence of psychoactive drugs and drugs of abuse).

EXCLUSION CRITERIA:

-Current alcohol or substance use or dependence (excluding nicotine) within the past 3 months of sufficient magnitude to require independent, concurrent treatment intervention (e.g. antabuse or opiate treatment, but not including self-help groups).

-Whether the minor lives with both parents or one parent, the parent(s) he/she lives with must have legal custody. If a parent has shared custody, both parents must consent to participate in this protocol.

-A current NIMH employee/staff or their immediate family member.


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Citations:

Not Provided

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Contacts:

Principal Investigator

Referral Contact

For more information:

Carlos A. Zarate, M.D.
National Institute of Mental Health (NIMH)
NIHBC 10 - CRC BG RM 7-5342
10 CENTER DR
BETHESDA MD 20892
(301) 326-5836
zaratec@mail.nih.gov

Carlos A. Zarate, M.D.
National Institute of Mental Health (NIMH)
NIHBC 10 - CRC BG RM 7-5342
10 CENTER DR
BETHESDA MD 20892
(301) 326-5836
moodresearch@mail.nih.gov

Maureen Tobin
National Institutes of Health
Building 10
Room 4C110
10 Center Drive
Bethesda, Maryland 20892
(301) 435-4518
adair@box-a.nih.gov

Clinical Trials Number:

NCT00024635

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