Center for Education and Drug Abuse Research (CEDAR): Etiological and Prospective Family Study in Southwestern Pennsylvania, Baseline Data, 1990-2011 (ICPSR 33444)
Principal Investigator(s): Tarter, Ralph E., University of Pittsburgh
The Center for Education and Drug Abuse Research (CEDAR) conducts research on 775 families enrolled in the Center's prospective investigations into the etiology of substance use disorder (SUD). The pro-bands are men with lifetime presence/absence of SUD consequent to use of an illicit drug who have a 10-12 year old biological son or daughter. The biological children of SUD men are assigned to the high average risk (HAR) group whereas offspring of men without SUD, having neither axis 1 disorder ("normal") nor SUD psychiatric disorder, are assigned to the low average risk (LAR) group. A second control group (Psych control) was also collected, in whom the fathers had a lifetime DSM-III-R diagnosis of any psychiatric disorder not related to substance use. The sample sizes are as follows: HAR = 344, LAR = 350, and Psych = 81. The children are currently in varying stages of follow-up evaluation conducted at ages 12-14, 16, 19, and annually thereafter until age 30. CEDAR has already shown that they can predict in 10-12 year old youth cannabis use disorder by age 22 with approximately 70 percent accuracy, thereby substantiating the paradigm, subject recruitment strategy, and measurement protocols. Multidisciplinary research is conducted on family members (father, mother, children) with the objective of elucidating the genetic, bio-behavioral, and environmental factors on development of SUD consequent to use of illegal drugs. Research protocols are organized into three thematically connected research modules (Neurogenetics, Developmental Psychopathology, and Translation) linking etiology and prevention. The research components thus align with the NIH Roadmap model such that basic science informs clinical research leading to prevention guided by an understanding of etiology. In addition to module-level research, faculty also participate in three organizational aims: (1) Devise a practical scale to quantify the transmissible liability to SUD; (2) Empirically test a bio-psychological theory of SUD etiology focusing on off-time maturation leading to psychological dysregulation predisposing to SUD; and, (3) Delineate SUD liability variants within an ontogenetic framework.
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Tarter, Ralph E. Center for Education and Drug Abuse Research (CEDAR): Etiological and Prospective Family Study in Southwestern Pennsylvania, Baseline Data, 1990-2011. ICPSR33444-v1. Ann Arbor, MI: Inter-university Consortium for Political and Social Research [distributor], 2012-08-10. http://doi.org/10.3886/ICPSR33444.v1
Persistent URL: http://doi.org/10.3886/ICPSR33444.v1
This study was funded by:
- United States Department of Health and Human Services. National Institutes of Health. National Institute on Drug Abuse (P50 DA 005605)
Scope of Study
Subject Terms: aptitude, attitudes, child health, children, cognition, cognitive functioning, domestic relations, drug abuse, drug use, families, family relations, health, mental health, parent child relationship, parents, participation, personality assessment, psychiatric services, psychological evaluation, psychological wellbeing, psychosocial assessment, social attitudes, social behavior, social life, substance abuse
Smallest Geographic Unit: Census tract
Geographic Coverage: Pennsylvania, United States
Date of Collection:
Unit of Observation: individual; household
Universe: Fathers, mothers, and biological children ages 10-12 in 1990 in Southeastern Pennsylvania whose father had a lifetime presence/absence of substance abuse disorder consequent to use of an illicit drug.
Data Types: survey data
Data Collection Notes:
For more information regarding the CEDAR study measures, users are encouraged to see the Center for Education and Drug Abuse Research (CEDAR) Web site.
Study Design: Three groups of male and female children are studied for a 20-year period: (1) Offspring of substance abusing fathers, (2) Offspring of normal fathers, and (3) Offspring of psychiatrically disturbed fathers. The three groups are longitudinally tracked from age 10-12 until they reach age 30 using the following assessment schedule: age 10-12, age 12-14, age 16, age 19-30 (with annual evaluations).
Sample: The sample uses a high risk paradigm, in which the families were selected based on a DSM-III-R diagnosis of substance use disorder in the biological father of the index child (High Average Risk, or HAR group) versus NO DSM-III-R psychiatric disorder (Low Average Risk, or LAR group). A second control group (Psych control) was also collected, in whom the fathers had a lifetime DSM-III-R diagnosis of any psychiatric disorder not related to substance use. The sample sizes are as follows: HAR = 344, LAR = 350, and Psych = 81. Citation: Tarter, R.E., Vanyukov, M.M. (2001). Introduction: Theoretical and operational framework for research into the etiology of substance use disorders. Journal of Child and Adolescent Substance Abuse 10 (4):1-12.
Time Method: Longitudinal: Panel: Continuous
Mode of Data Collection: cognitive assessment test, face-to-face interview, mail questionnaire, paper and pencil interview (PAPI), on-site questionnaire, telephone interview
Presence of Common Scales: This study utilized the following measurement tools: Child Behavior Checklist (CBCL), Dimensions of Temperament - Revised (DOTs-R), Family Assessment Measure (FAM), Health Problems Checklist (HPQ), and Multidimensional Personality Questionnaire (MPQ).
Extent of Processing: ICPSR data undergo a confidentiality review and are altered when necessary to limit the risk of disclosure. ICPSR also routinely creates ready-to-go data files along with setups in the major statistical software formats as well as standard codebooks to accompany the data. In addition to these procedures, ICPSR performed the following processing steps for this data collection:
- Created variable labels and/or value labels.
- Standardized missing values.
- Checked for undocumented or out-of-range codes.
Original ICPSR Release: 2012-08-10
Related Publications (?)
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