Genetics of Recurrent Early-Onset Depression

NCT ID: NCT00005914

Last Updated: 2019-04-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

2533 participants

Study Classification

OBSERVATIONAL

Study Start Date

1999-10-31

Study Completion Date

2005-10-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This nationwide study will create a DNA collection to permit qualified scientists to search for depression-related genes.

More than 750 families with at least two siblings who have experienced major depression are needed for the study. Participants will be interviewed about psychiatric and family history, and will be asked to provide a small blood specimen. The identification of predisposing genes can lead to greater understanding of the brain mechanisms involved in severe depression which can in turn lead to the discovery of new treatments.

A Certificate of Confidentiality from the federal government ensures that all information will be strictly confidential. Blood specimens are identified only by code number (not by name).

Reimbursement is provided.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Studies of patterns of major depression in families suggest that 50 to 70% of the predisposition to major depression is caused by genes. People with recurrent depression and earlier ages of onset have more relatives with depression. There are probably at least several interacting genes, rather than a single gene as in some disorders. The identification of predisposing genes is likely to lead to greater understanding of the brain mechanisms involved in severe depression. This could lead to the discovery of new treatments.

This study will create a DNA collection to permit qualified scientists to search for depression-related genes. More than 750 families with at least two siblings who have experienced major depression are needed for the study.

Participants in this study will be interviewed about psychiatric and family history, and will be asked for a small blood specimen. Interviews can be conducted in person or by telephone. For telephone interviews, blood sample collection will be arranged at a location and time convenient for the participant. Participants will also be asked for help in inviting other family members to participate. No family member will be contacted without the permission and assistance of another participating family member.

For information on a related study, please follow this link:

http://clinicaltrials.gov/show/NCT00260182

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Depression

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

FAMILY_BASED

Study Time Perspective

RETROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Probands and family members

Individuals with major depressive disorder who meet study criteria, and members of their families. No intervention. This is a genetic study only.

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Families that have at least TWO ADULT SIBLINGS (brother/brother; sister/sister; brother/sister) who have experienced major depression.
* Depression must be RECURRENT (more than one episode).
* Depression must have started at age 30 or less in one sibling, and at age 40 or less in the other sibling.

Exclusion Criteria

* Participants cannot have Bipolar I (manic-depressive) disorder or schizophrenia.
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

National Institute of Mental Health (NIMH)

NIH

Sponsor Role collaborator

Stanford University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Douglas F. Levinson

Principle Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Myrna Weissman

Role: PRINCIPAL_INVESTIGATOR

Columbia University

J R DePaulo

Role: PRINCIPAL_INVESTIGATOR

Johns Hopkins University

William Scheftner

Role: PRINCIPAL_INVESTIGATOR

Rush University Hospital

Raymond Crowe

Role: PRINCIPAL_INVESTIGATOR

University of Iowa

Douglas Levinson

Role: PRINCIPAL_INVESTIGATOR

University of Pennsylvania

George Zubenko

Role: PRINCIPAL_INVESTIGATOR

University of Pittsburgh

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Rush Presbyterian - Saint Luke's Med Ctr

Chicago, Illinois, United States

Site Status

Univ of Iowa Hosp and Clinic

Iowa City, Iowa, United States

Site Status

Johns Hopkins University

Baltimore, Maryland, United States

Site Status

New York State Psychiatric Institute / Columbia Univ

New York, New York, United States

Site Status

Univ of Pennsylvania

Philadelphia, Pennsylvania, United States

Site Status

Univ of Pittsburgh / Western Psychiatric Inst and Clinic

Pittsburgh, Pennsylvania, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Related Links

Access external resources that provide additional context or updates about the study.

http://nyspi.org

Web site for New York Psychiatric Institute

http://www.medicine.uiowa.edu/psychiatry/

Web site for University of Iowa

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

R01MH061686-01

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH060912

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH059552

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH059541

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH059542

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH061686

Identifier Type: NIH

Identifier Source: secondary_id

View Link

R01MH060866

Identifier Type: NIH

Identifier Source: secondary_id

View Link

DNBBS 7G-GRR

Identifier Type: -

Identifier Source: secondary_id

R01MH061686-01

Identifier Type: NIH

Identifier Source: org_study_id

View Link

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.