Bay Area Health Task Force Small Employers' Health Insurance Helpline Database, 1989-1992 (ICPSR 6112)
Robert Wood Johnson Foundation Supportive Services Program in Senior Housing, Tenant Characteristics and Service Use, 1990-1991: [United States] (ICPSR 6013)
National Survey of Children: Wave I, 1976, Wave II, 1981, and Wave III, 1987 (ICPSR 8670)
Robert Wood Johnson Foundation Supportive Services for Older Persons Program, 1988-1991: [United States] (ICPSR 9946)
National School Health Services Program Evaluation, 1981-1982 (ICPSR 8302)
Evaluation of Regionalized Networks of High-Risk Pregnancy Care, 1970-1979 (ICPSR 8469)
Impact of the NYC Sugar Sweetened Beverage Policy on Calories Purchased and Consumed: Data on Fast Food Purchases, Dietary Patterns, and Retail Beverage Environments in New York City, Newark, and Jersey City, 2013-2014 (ICPSR 37143)
The current collection includes data collected as part of a planned evaluation of New York City's proposed soda portion cap policy. Baseline data collection was conducted in three waves. Wave 1 began in early January 2013 and ended in April 2013; Wave 2 was conducted from August to November 2013; and Wave 3 was conducted between January and June 2014.
Data was collected at point-of-purchase on the availability, sizing, promotion, and cost of beverages in the fast food restaurants of New York City, New York and of Newark and Jersey City in New Jersey. This data was also collected in these areas for their nearest convenience stores/bodegas and supermarkets. Consumer receipts were also gathered to supplement this survey data. Additional data collection was conducted using environmental scans of fast food and grocery store locations to evaluate the healthfulness of the beverage environment. Lastly, some participants also completed a telephone interview where data was gathered on participant's dietary recall.
These data are intended to gather a fuller picture of the factors that may influence beverage purchases.
Creating a Patient Registry to Facilitate Data Sharing and Encourage Patient-Centered Approaches to Improving Health and Lowering Costs, 2013 (ICPSR 35570)
This interventional pilot study was conducted in a primary care clinic to determine if patients would become more engaged in their own health and ask more questions of their physicians if they were provided data about patients similar to themselves. The study was conducted with 150 patients with a diagnosis of hypertension who had scheduled appointments with one of three participating physicians in the clinic. When they arrived at the clinic for their appointment, the patients were shown de-identified clinical data about similar patients with hypertension on a computer screen, given a printout of this information, and then proceeded to visit their physician. After the physician visit the patients completed a short survey. Their answers to the survey questions are recorded in the data file together with additional information about them, such as age, gender, race, smoking status and comorbidities.
The three participating physicians completed a short survey at the end of the study. The results of that survey are summarized in a table provided with the technical documentation.