MyData:What Is MyData? | Login/Account Info | Download Saved Files | Logout Description & Citation--Study No. 13614 | | | ICPSR Study No.: | 13614 |
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Persistent URL:
| http://dx.doi.org/10.3886/ICPSR13614 |
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| | | Title: | Project on Human Development in Chicago Neighborhoods (PHDCN): Depression, Wave 2, 1997-2000 |
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| | | Alternate Title: | PHDCN DEP, 1997-2000 |
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| | | Principal Investigator(s): | Felton J. Earls, Harvard Medical School |
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| Jeanne Brooks-Gunn, Scientific Director. Columbia University. Teacher's College. Center for the Study of Children and Families |
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| Stephen W. Raudenbush, Scientific Director. University of Michigan. School of Education and Survey Research Center |
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| Robert J. Sampson, Scientific Director. Harvard University. Department of Sociology |
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| | | Series: | Project on Human Development in Chicago Neighborhoods (PHDCN) Series |
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| | | Funding Agency: | John D. and Catherine T. MacArthur Foundation |
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| Child Care Bureau |
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| Harris Foundation |
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| Head Start Bureau of the Administration for Children and Families |
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| National Institute of Child Health and Human Development |
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| National Institute for Early Child Development and Education |
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| National Institute of Justice |
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| National Institute of Mental Health |
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| Office of Education Research and Improvement of the United States Department of Education |
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| Turner Foundation |
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| | | Grant Number: | 93-IJ-CX-K005 |
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| | | Bibliographic Citation: | Earls, Felton J., Jeanne Brooks-Gunn, Stephen W. Raudenbush, and Robert J. Sampson. PROJECT ON HUMAN DEVELOPMENT IN CHICAGO NEIGHBORHOODS (PHDCN): DEPRESSION, WAVE 2, 1997-2000 [Computer file]. ICPSR13614-v1. Boston, MA: Harvard Medical School [producer], 2002. Ann Arbor, MI: Inter-university Consortium for Political and Social Research [distributor], 2005-11-14. doi:10.3886/ICPSR13614 |
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| | | | Summary: | The Project on Human Development in Chicago Neighborhoods
(PHDCN) was a large-scale, interdisciplinary study of how families,
schools, and neighborhoods affect child and adolescent development.
One component of the PHDCN was the Longitudinal Cohort Study, which
was a series of coordinated longitudinal studies that followed over
6,000 randomly selected children, adolescents, and young adults, and
their primary caregivers over time to examine the changing
circumstances of their lives, as well as the personal characteristics,
that might lead them toward or away from a variety of antisocial
behaviors. Numerous measures were administered to respondents to
gauge various aspects of human development, including individual
differences, as well as family, peer, and school influences. The
Depression survey was administered to subjects' primary caregivers for
Cohorts 0 to 15. The instrument was adapted from the short form of the
Composite International Diagnostic Interview (UM-CIDI) and obtained
information about depressive symptoms experienced by the primary
caregiver during the past year. |
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| | | Subject Term(s): | antidepressants, caregivers, depression (psychology), emotional states, social behavior |
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| | | Geographic Coverage: | Chicago, Illinois, United States |
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| | | Time Period: | 1997 - 2000 |
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| | | Date(s) of Collection: | 1997 - 2000 |
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| | | Unit of Observation: | individual |
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| | | Universe: | Children, adolescents, young adults, and their primary
caregivers, living in the city of Chicago in 1994. |
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| | | Data Type: | survey data |
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| | | Data Collection Notes: | The Murray Research Center conducted the initial data
and documentation processing for this collection. |
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| | | | Purpose of the Study: | Project on Human Development in Chicago
Neighborhoods
The Project on Human Development in Chicago Neighborhoods (PHDCN)
was a large-scale, interdisciplinary study of how families, schools,
and neighborhoods affect child and adolescent development. It was
designed to advance the understanding of the developmental pathways of
both positive and negative human social behaviors. In particular, the
project examined the causes and pathways of juvenile delinquency,
adult crime, substance abuse, and violence. At the same time, the
project provided a detailed look at the environments in which these
social behaviors took place by collecting substantial amounts of data
about urban Chicago, including its people, institutions, and
resources.
Longitudinal Cohort Study
One component of the PHDCN was the Longitudinal Cohort Study, which
was a series of coordinated longitudinal studies that followed over
6,000 randomly selected children, adolescents, and young adults, and
their primary caregivers over time to examine the changing
circumstances of their lives, as well as the personal characteristics,
that might lead them toward or away from a variety of antisocial
behaviors. The age cohorts include birth (0), 3, 6, 9, 12, 15, and 18
years. Numerous measures were administered to respondents to gauge
various aspects of human development, including individual
differences, as well as family, peer, and school influences.
Depression
The data in this collection are from Wave 2 of the Longitudinal
Cohort Study, which was administered between 1997 and 2000. The data
files contain information from the Depression protocol. The Depression
instrument was administered to subjects' primary caregivers for
Cohorts 0 to 15. The instrument was adapted from the short form of the
Composite International Diagnostic Interview (UM-CIDI) and obtained
information about depressive symptoms experienced by the primary
caregiver during the past year. |
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| | | Study Design: | Project on Human Development in Chicago
Neighborhoods
The city of Chicago was selected as the research site for the PHDCN
because of its extensive racial, ethnic, and social-class diversity.
The project collapsed 847 census tracts in the city of Chicago into
343 neighborhood clusters (NCs) based upon seven groupings of
racial/ethnic composition and three levels of socioeconomic
status. The NCs were designed to be ecologically meaningful. They were
composed of geographically contiguous census tracts, and geographic
boundaries, and knowledge of Chicago's neighborhoods were considered
in the definition of the NCs. Each NC was comprised of approximately
8,000 people.
Longitudinal Cohort Study
For the Longitudinal Cohort Study, a stratified probability sample
of 80 neighborhoods was selected. The 80 NCs were sampled from the 21
strata (seven racial/ethnic groups by three socioeconomic levels) with
the goal of representing the 21 cells as equally as possible to
eliminate the confounding between racial/ethnic mix and socioeconomic
status. Once the 80 NCs were chosen, then block groups were selected
at random within each of the sample neighborhoods. A complete listing
of dwelling units was collected for all sampled block groups.
Pregnant women, children, and young adults in seven age cohorts
(birth, 3, 6, 9, 12, 15, and 18 years) were identified through
in-person screening of approximately 40,000 dwelling units within the
80 NCs. The screening response rate was 80 percent. Children within
six months of the birthday that qualified them for the sample were
selected for inclusion in the Longitudinal Cohort Study. A total of
8,347 participants were identified through the screening. Of the
eligible study participants, 6,228 were interviewed in the Wave 1 data
collection and 5,338 were interviewed in the Wave 2 data
collection.
Data collection for Wave 2 began in 1997 and ended in 2000. It
included a letter sent to study participants notifying them that they
would be contacted to schedule an interview. This letter explained the
study, reimbursements, and offered a monthly drawing prize of $1,000
for those participants who kept their first scheduled appointment. A
toll free number was also included in the letter, so participants
could call and schedule their own interviews or ask questions.
For all cohorts except 0 and 18, primary caregivers as well as the
child were interviewed. The primary caregiver was the person found to
spend the most time taking care of the child. Separate research
assistants administered the primary caregiver interviews and the child
interviews. The primary method of data collection was face-to-face
interviewing, although participants who refused to complete the
personal interview were administered a phone interview. An abbreviated
telephone interview was conducted for the primary caregivers in
Cohorts 0-15 and Cohort 18 study participants in Wave 2 who lived
outside the nine-county metropolitan area to which research assistants
were able to travel for interviews. A total of 221 telephone
interviews were conducted during Wave 2, representing 3.55 percent of
the sample.
Proxy interviews were conducted with study participants who were
emancipated minors (under 18 but married or living independently). The
study participants answered questions from the primary caregiver's
interview on the primary caregiver's behalf. In Wave 2, four primary
caregivers and two study participants were interviewed in jail. Study
participants in foster care could not be interviewed. The Department
of Children and Family Services did not allow interviews of the foster
parent or the child. Permission was granted for a brief period in
Wave 1, therefore there are some children in the sample who could not
be followed up in Waves 2 and 3. Some children were not in foster care
in Wave 1 but were placed in foster care by Wave 2 or 3. They were
also not followed up. Lastly, some participants were interviewed in
Wave 3 but not in Wave 2, as they were in foster care during Wave 2.
Some participants in Wave 1 spoke a language other than English,
Spanish, or Polish. In Wave 2, an abbreviated version of the primary
caregiver's protocol was administered, and the research assistant
arranged for someone in the household to translate on the spot. In
Wave 2, the complete protocol was translated into Spanish, and a
subset of the primary caregiver's interview was translated into
Polish.
Depending on the age and wave of data collection, participants were
paid between $5 and $20 per interview. Other incentives, such as free
passes to museums, the aquarium, and monthly drawing prizes, were also
included.
Interview protocols included a wide range of questions. For
example, some questions assessed impulse control and sensation-seeking
traits, cognitive and language development, leisure activities,
delinquency and substance abuse, friends' activities, and
self-perception, attitudes, and values. Caregivers were also
interviewed about family structure, parent characteristics,
parent-child relationships, parent discipline styles, family mental
health, and family history of criminal behavior and drug use.
Depression
The Depression survey was administered to subjects' primary
caregivers for Cohorts 0 to 15. The instrument was adapted from the
short form of the Composite International Diagnostic Interview
(UM-CIDI), and obtained information about depressive symptoms
experienced by the primary caregiver during the past year. |
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| | | Sample: | Stratified probability sample. |
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| | | Weight: | none |
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| | | Mode of Data Collection: | face-to-face interview |
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| telephone interview |
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| | | Description of Variables: | The data files contain information regarding
depressive symptoms experienced by the primary caregiver during the
past year. Respondents were asked if they felt sad, blue, or
depressed for two weeks or more during the past year. Follow-up
questions were asked regarding the two-week period when these feelings
were worst including the daily duration and frequency of these
feelings, as well as whether the respondent lost interest in things,
was more tired, had changes in weight, had trouble sleeping, had
trouble concentrating, felt worthless, or thought about death. The
files also contain information about how many weeks the respondent
felt this way in the past year, when the most recent two-week period
was, whether the respondent told a doctor or other professional about
these feelings, whether the respondent took medication or drugs for
these problems, and how much these problems interfered with their
life. Nearly the same set of questions was asked regarding any
two-week period when the respondent lost interest in most things like
hobbies, work, or activities that usually gave them pleasure. |
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| | | Response Rates: | The overall response rate for Wave 2 of the
Longitudinal Cohort Study was 85.94 percent or 5,338 participants. The
response rates for subjects by cohort were:
- 0 percent for Cohort 0
- 87.5 percent for Cohort 3
- 88.0 percent for Cohort 6
- 85.6 percent for Cohort 9
- 86.2 percent for Cohort 12
- 82.7 percent for Cohort 15
- 80.2 percent for Cohort 18
The response rates for primary caregivers by cohort were:
- 83.3 percent for Cohort 0
- 88.3 percent for Cohort 3
- 88.3 percent for Cohort 6
- 86.6 percent for Cohort 9
- 87.2 percent for Cohort 12
- 85.9 percent for Cohort 15
- 0 percent for Cohort 18
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| | | Presence of Common Scales: | Composite International Diagnostic Interview (UM-CIDI) |
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| | | | Note: | A list of the data formats available for this study can be found in the
summary of holdings. Detailed file-level information (such as record length, case count, and variable count) is listed in the
file manifest. |
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Some instruments administered as part of this
study may contain contents from copyrighted
instruments. Reproductions of the instruments
are provided solely as documentation for
the analysis of the data associated with this
collection. Please contact the data producers for
information on permissions to use the instruments
for other purposes.
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| | | Restrictions: | To protect respondent privacy, certain identifying
information is restricted from general dissemination. Specifically,
ID variables which link data across waves and the month and year
variables are restricted. Users interested in obtaining these data
must complete a Data Transfer Agreement Form and specify the reasons
for the request. A copy of the Data Transfer Agreement Form can be
requested by calling 800-999-0960. The Data Transfer Agreement Form is
also available as a Portable Document Format (PDF) file from the
NACJD Web site (link). Completed forms should be returned to: Director,
National Archive of Criminal Justice Data, Inter-university Consortium
for Political and Social Research, Institute for Social Research, P.O.
Box 1248, University of Michigan, Ann Arbor, MI 48106-1248, or by fax:
734-647-8200. |
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| | | Original ICPSR Release: | 2005-11-14 |
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| | | Dataset(s): | - DS1: Cohort 0
- DS2: Cohort 3
- DS3: Cohort 6
- DS4: Cohort 9
- DS5: Cohort 12
- DS6: Cohort 15
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