National Institute of Mental Health Collaborative Psychiatric Epidemiology Surveys (CPES)

Study Overview

Description: 

The Collaborative Psychiatric Epidemiology Surveys (CPES), with support from NIMH, were initiatied in recognition of the need for contempary, comprehensive epidemiological data regarding the distributions, correlates, and risk factors of mental disorders among the general population with special emphasis on minority groups. The primary objective of the CPES was to collect data about the prevalanece of mental disorders, impairments associated with these disorders, and their treatment patterns from representative samples of majority and minority adult populations in the U.S. Secondary goals were to obtain information about language use and ethnic disparities, support systems, discrimination, and assimilation, in order to examine whether and how closely various mental health disorders are linked to social and cultural issues. The data was obtained through three nationally representative surveys: the National Comorbidity Survey Replication (NCS-R), the National Survey of American Life (NSAL), and the National Latino and Asian American Study (NLAAS).

Sampling Procedures: 

The selection of a probability sample of respondents for each study's interview required a four-step sampling process: 1) a primary stage sampling of U. S. Metropolitan Statistical Areas (MSAs) and counties; 2) a second stage sampling of area segments; 3) a sampling of housing units within the area segments; 4) random selection of eligible respondents from the housing units. Adults aged 18 and older were available for the surveys some also had restrictions by race/ethnicity.

Contact and Data Access

Conditions: 
1. I will use the dataset solely for statistical analysis and reporting of aggregated information and not for investigation of a specific individual or organization. 2. I will produce no links among the Distributors' datasets or among the Distributor's data and other datasets that could identify individuals or organizations. 3. I represent neither I, nor anyone I know, has any prior knowledge of the possible identification of any study participants in any dataset that I am being licensed to use. 4. I will not knowingly divulge any information that could be used to identify individual participants in the study, nor will I attempt to identify or contact any study participant and I agree to use any precautions necessary to prevent such identification. 5. I will not reproduce the dataset except as it is necessary for scholarly purposes. I will destroy the dataset upon completion of my scholarly work with it. 6. I will not share data from the dataset (in any form or by any means) with any third party, as I understand that all users of the data must obtain it directly from the distributor. 7. I will make appropriate acknowledgement of the contributor and distributor of the dataset in any manuscript or publication. 8. The distributor makes no warranties, express or implied, by operation of law or otherwise regarding or relating to the dataset.
Disclaimer: 
The original collector of the data, SSRI, and the relevant funding agencies, bear no responsibility for the use of the data or for interpretations and inferences based upon such users.

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