Data Collection Methods in Establishment Surveys
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Data Collection WP Template
Distr. GENERAL 02 September 2013 WP 14 ENGLISH ONLY UNITED NATIONS ECONOMIC COMMISSION FOR EUROPE CONFERENCE OF EUROPEAN STATISTICIANS Seminar on Statistical Data Collection (Geneva, Switzerland, 25-27 September 2013) Topic (ii): Managing data collection functions in a changing environment THE BUSINESS STATISTICAL PORTAL: A NEW WAY OF ORGANIZING AND MANAGING DATA COLLECTION PROCESSES FOR BUSINESS SURVEYS IN ISTAT Working Paper Prepared by Natale Renato Fazio, Manuela Murgia, Andrea Nunnari, ISTAT – Italian National Statistical Institute I. Introduction 1. A broad shift of the social and technological context requires ISTAT to modify the way data are collected in order to improve the efficiency in producing timely estimates and, at the same time, to increase or at least maintain the level of data quality, while reducing respondent burden. All of this, within a climate of general budgets cuts. 2. In 2010, as a way to deal with these challenges, a medium-long term project was launched (Stat2015), envisaging the gradual standardisation and industrialisation of the entire cycle of ISTAT statistical processes, according to a model based on a metadata-driven, service-oriented architecture. With regard to data collection, as well for the other production phases, Stat2015 aims at outlining strong enterprise architecture standards. 3. A first step along these lines was to develop a comprehensive set of requirements according to which select, design or further develop the IT tools supporting data collection. The requirements encompassed four areas, covering the main functions of the entire (data collection) process: i) Survey unit management, ii) Data collection management, iii) Questionnaire, iv) Communication facilities. 4. A significant contribution to the definition and implementation of these requirements came with the development of the new ISTAT Business Statistical Portal, a single entry point for Web-based data collection from enterprises, which is at the same time an attempt to streamline the organization and management of business surveys as a whole. -
Questionnaire Design Guidelines for Establishment Surveys
Journal of Official Statistics, Vol. 26, No. 1, 2010, pp. 43–85 Questionnaire Design Guidelines for Establishment Surveys Rebecca L. Morrison1, Don A. Dillman2, and Leah M. Christian3 Previous literature has shown the effects of question wording or visual design on the data provided by respondents. However, few articles have been published that link the effects of question wording and visual design to the development of questionnaire design guidelines. This article proposes specific guidelines for the design of establishment surveys within statistical agencies based on theories regarding communication and visual perception, experimental research on question wording and visual design, and findings from cognitive interviews with establishment survey respondents. The guidelines are applicable to both paper and electronic instruments, and cover such topics as the phrasing of questions, the use of space, the placement and wording of instructions, the design of answer spaces, and matrices. Key words: Visual design; question wording; cognitive interviews. 1. Introduction In recent years, considerable effort has been made to develop questionnaire construction guidelines for how questions should appear in establishment surveys. Examples include guidelines developed by the Australian Bureau of Statistics (2006) and Statistics Norway (Nøtnæs 2006). These guidelines have utilized the rapidly emerging research on how the choice of survey mode, question wording, and visual layout influence respondent answers, in order to improve the quality of responses and to encourage similarity of construction when more than one survey data collection mode is used. Redesign efforts for surveys at the Central Bureau of Statistics in the Netherlands (Snijkers 2007), Statistics Denmark (Conrad 2007), and the Office for National Statistics in the United Kingdom (Jones et al. -
Standardization and Harmonization of Data and Data Collection Initiatives
Conference of the Parties to the WHO Framework Convention on Tobacco Control Fourth session FCTC/COP/4/15 Punta del Este, Uruguay, 15–20 November 2010 15 August 2010 Provisional agenda item 6.2 Standardization and harmonization of data and data collection initiatives Report of the Convention Secretariat INTRODUCTION 1. At its third session (Durban, South Africa, 17–22 November 2008) the Conference of the Parties requested the Convention Secretariat to compile a report on data collection measures, in decision FCTC/COP3(17). The decision outlined the fact that this should be undertaken under the guidance of the Bureau, and with the assistance of competent authorities within WHO, in particular WHO’s Tobacco Free Initiative, as well as relevant intergovernmental and nongovernmental organizations with specific expertise in this area. Paragraph 6 of the decision stated that the report should cover measures: to improve the comparability of data over time; to standardize1 collected data within and between Parties; to develop indicators and definitions to be used by Parties’ national and international data collection initiatives; and to further harmonize2 with other data collection initiatives. 2. The request to provide such a report is in line with Article 23.5 of the Convention, which requires the Conference of the Parties to “keep under regular review the implementation of the Convention” and to “promote and guide the development and periodic refinement of comparable methodologies for research and the collection of data, in addition to those provided for in Article 20, relevant to the implementation of the Convention”. 1 Standardization: the adoption of generally accepted uniform technical specifications, criteria, methods, processes or practices to measure an item. -
Data Collection and Analysis Plan FAMILY OPTIONS STUDY
Data Collection and Analysis Plan FAMILY OPTIONS STUDY UU.S..S. DDepaepartmentrtment ofof HouHousingsing andand UrUrbanban DevDevelopelopmmentent || OOfficeffice ofof PolicPolicyy DevDevelopelopmentment andand ResReseaearchrch Visit PD&R’s website www.huduser.org to find this report and others sponsored by HUD’s Office of Policy Development and Research (PD&R). Other services of HUD USER, PD&R’s research information service, include listservs, special interest reports, bimonthly publications (best practices, significant studies from other sources), access to public use databases, and a hotline (800-245-2691) for help accessing the information you need. Data Collection and Analysis Plan FAMILY OPTIONS STUDY Prepared for: U.S. Department of Housing and Urban Development Washington, D.C. Prepared by: Abt Associates Inc. Daniel Gubits Michelle Wood Debi McInnis Scott Brown Brooke Spellman Stephen Bell In partnership with : Vanderbilt University Marybeth Shinn March 2013 Disclaimer Disclaimer The contents of this report are the views of the authors and do not necessarily reflect the views or policies of the U.S. Department of Housing and Urban Development or the U.S. Government. Family Options Study Data Collection and Analysis Plan Table of Contents Family Options Study Revised Data Collection and Analysis Plan Table of Contents Chapter 1. Introduction and Evaluation Design .................................................................................. 1 1.1 Overview and Objectives ........................................................................................................ -
Ground Data Collection and Use
ANDREWS. BENSON WILLIAMC. DRAEGER LAWRENCER. PETTINGER University of California* Berkeley, Calif. 94720 Ground Data Collection and Use These are essential components of an agricultural resource survey. INTRODUCTION sions based on their efforts to perform re- HE IMPORTANCE OF collecting meaningful gional agricultural inventories in Maricopa T and timely ground data for resource in- County, Arizona, using space and high-alti- ventories which employ remote sensing tech- tude aerial photography, as part of an ongoing niques is often discussed, and appropriately NASA-sponsored research project (Draeger, so. However, those wishing to conduct inven- et a]., 1970). This paper draws upon examples tories frequently fail to devote as much time from this research. However, much of the dis- to the planning of field activities which occur cussion is relevant to other disciplines for in conjunction with an aircraft mission as which ground data is important. they do in planning the flight itself. As a re- sult. adequate remote sensing data mav be collected,-but no adequate sipporting infor- Preliminary evaluation of the geographical ABSTRACT:During the past two years, extensive studies have been conducted out in the Phoenix, Arizona area to ascertain the degree to which sequential high- altitude aircraft and spacecraft imagery can contribute to operational agri- cultural crop surveys. Data collected on the ground within the test site con- stituted an essential component of the three phases of the survey: (I)farniliariza- tion with the area and design of preliminary evalz~ationexperiments, (2) train- in,g of interpreters, and (3)providing the basis upon which image interpretation estimates can be adjusted and evaluated. -
Design and Implementation of N-Of-1 Trials: a User's Guide
Design and Implementation of N-of-1 Trials: A User’s Guide N of 1 The Agency for Healthcare Research and Quality’s (AHRQ) Effective Health Care Program conducts and supports research focused on the outcomes, effectiveness, comparative clinical effectiveness, and appropriateness of pharmaceuticals, devices, and health care services. More information on the Effective Health Care Program and electronic copies of this report can be found at www.effectivehealthcare.ahrq. gov. This report was produced under contract to AHRQ by the Brigham and Women’s Hospital DEcIDE (Developing Evidence to Inform Decisions about Effectiveness) Methods Center under Contract No. 290-2005-0016-I. The AHRQ Task Order Officer for this project was Parivash Nourjah, Ph.D. The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views ofAHRQ or the U.S. Department of Health and Human Services. Therefore, no statement in this report should be construed as an official position of AHRQ or the U.S. Department of Health and Human Services. Persons using assistive technology may not be able to fully access information in this report. For assistance contact [email protected]. The following investigators acknowledge financial support: Dr. Naihua Duan was supported in part by NIH grants 1 R01 NR013938 and 7 P30 MH090322, Dr. Heather Kaplan is part of the investigator team that designed and developed the MyIBD platform, and this work was supported in part by Cincinnati Children’s Hospital Medical Center. Dr. Richard Kravitz was supported in part by National Institute of Nursing Research Grant R01 NR01393801. -
Interactive Voice Response for Data Collection in Low and Middle-Income Countries
Interactive Voice Response for Data Collection in Low and Middle-Income Countries Viamo Brief April 2018 Suggested Citation Greenleaf, A.R. Vogel, L. 2018. Interactive Voice Response for Data Collection in Low and Middle- Income Countries. Toronto, Canada: Viamo. 1 0 - EXECUTIVE SUMMARY Expanding mobile network coverage, decreasing cost of cellphones and airtime, and a more literate population have made mobile phone surveys an increasingly viable option for data collection in low- and middle-income countries (LMICs). Interactive voice response (IVR) is a fast and cost-effective option for survey data collection. The benefits of trying to reach respondents in low and middle-income countries (LMICs) via cell phone have been described by The World Bank,[1] academics[2,3], and practitioners[4] alike. IVR, a faster and less expensive option than face-to-face surveys, can collect data in areas that are difficult for human interviewers to reach. This brief explains applications of IVR for data collection in LMICs. Sections 1- 4 provide background information about IVR and detail the advantages of “robo-calls”. The next three sections explain the three main target groups for IVR. Beginning with Section 5 we outline the four approaches to sampling a general population and address IVR data quality. Known respondents, who are often enrolled for monitoring and evaluation, are covered in Section 6, along with best practices for maximizing participant engagement. Finally, in Section 7 we explain how professionals use IVR for surveillance and reporting. Woven throughout Sections 5-7, four case studies illustrate how four organizations have successfully used IVR to for data collection. -
When Should We Ask, When Should We Measure?
Page 1 – CONGRESS 2015 Copyright © ESOMAR 2015 WHEN SHOULD WE ASK, WHEN SHOULD WE MEASURE? COMPARING INFORMATION FROM PASSIVE AND ACTIVE DATA COLLECTION Melanie Revilla • Carlos Ochoa • Roos Voorend • Germán Loewe INTRODUCTION Different sources of data Questionnaires have been a fundamental tool for market research for decades. With the arrival of internet, the questionnaire, a tool invented more than 100 years ago, was simply adapted to online data collection. The arrival of online panels in the 2000s meant an important boost for online questionnaires, and as a consequence, the tipping point for their online migration. We have come this far making all kind of market research projects using almost always the same tool. But this does not mean there is no room or need for improvement. If researchers massively used questionnaires during all these years, it is not because this is the most suited data collection tool for all the problems they faced; but because there were no better alternatives available. In addition, nowadays, things are changing really fast. This affects survey-based market research, particularly when the data collection process relies on respondent’s memory. A tool that was working reasonably in the past may not be sufficient anymore. Indeed, in the last decades, with the development of new technologies, an increased part of the consumer activity takes place on the internet. Also, we have witnessed an explosion of relevant events for marketing: increased consumer ad exposure through multiple channels, increased availability of products and brands, complex and quick decision making processes, etc. Larger memory issues may be expected in this new situation. -
Collapsing the Distinction Between Experimentation and Treatment in the Regulation of New Drugs
File: LAAKMANN EIC PUBLISH.doc Created on: 3/30/2011 4:56:00 PM Last Printed: 4/7/2011 11:58:00 AM COLLAPSING THE DISTINCTION BETWEEN EXPERIMENTATION AND TREATMENT IN THE REGULATION OF NEW DRUGS Anna B. Laakmann* The explosion of scientific knowledge in recent decades has simulta- neously increased pressure on the Food and Drug Administration (FDA) both to expedite market entry of promising medical breakthroughs and to safeguard the public from harms caused by new products. Ironically, as the FDA and drug manufacturers spend huge sums in the premarketing phase gathering and interpreting data from planned trials, an enormous amount of valuable information about postmarketing clinical experiences with FDA-regulated drugs is not being effectively captured. The Article asserts that the FDA should formally recognize the blurred line between experimentation and treatment by adopting a more fluid approach to its review of new medical technologies. It argues that the FDA should shift its focus toward harnessing and distilling accumulated experiential knowledge about the effects of new drugs so as to enable patients and doctors to make rational treatment decisions based on inevitably imperfect information. The Article sets forth an alternative regulatory approach that seamlessly incor- porates prospective outcomes data into the FDA drug review process. This approach would be facilitated by the creation of a centralized database that serves as a clearinghouse of information about treatment outcomes. The proposed scheme would help to address current failures in the imple- mentation of the agency’s “fast-track” programs. More broadly, it could serve as the instrumentality to effectuate a shift in the perceived role of the FDA from market gatekeeper to consolidator and purveyor of information about drug safety and efficacy. -
(EPOC) Data Collection Checklist
Cochrane Effective Practice and Organisation of Care Review Group DATA COLLECTION CHECKLIST Page 2 Cochrane Effective Practice and Organisation of Care Review Group (EPOC) Data Collection Checklist CONTENTS Item Page Introduction 5-6 1 Inclusion criteria* 7-8 1.1 Study design* 7 1.1.1 Randomised controlled trial* 1.1.2 Controlled clinical trial* 1.1.3 Controlled before and after study* 1.1.4 Interrupted time series* 1.2 Methodological inclusion criteria* 8 2 Interventions* 9-12 2.1 Type of intervention 9 2.1.1 Professional interventions* 9 2.1.2 Financial interventions* 10 2.1.2.1 Provider interventions* 2.1.2.2 Patient interventions* 2.1.3 Organisational interventions* 11 2.1.3.1 Provider orientated interventions* 2.1.3.2 Patient orientated interventions* 2.1.3.3 Structural interventions* 2.1.4 Regulatory interventions* 12 2.2 Controls* 13 3 Type of targeted behaviour* 13 4 Participants* 14-15 4.1 Characteristics of participating providers* 14 4.1.1 Profession* Item Page Page 3 4.1.2 Level of training* 4.1.3 Clinical speciality* 4.1.4 Age 4.1.5 Time since graduation 4.2 Characteristics of participating patients* 15 4.2.1 Clinical problem* 4.2.2 Other patient characteristics 4.2.3 Number of patients included in the study* 5 Setting* 16 5.1 Reimbursement system 5.2 Location of care* 5.3 Academic Status* 5.4 Country* 5.5 Proportion of eligible providers from the sampling frame* 6 Methods* 17 6.1 Unit of allocation* 6.2 Unit of analysis* 6.3 Power calculation* 6.4 Quality criteria* 17-22 6.4.1 Quality criteria for randomised controlled trials -
Patient Reported Outcomes (PROS) in Performance Measurement
Patient-Reported Outcomes Table of Contents Introduction ............................................................................................................................................ 2 Defining Patient-Reported Outcomes ............................................................................................ 2 How Are PROs Used? ............................................................................................................................ 3 Measuring research study endpoints ........................................................................................................ 3 Monitoring adverse events in clinical research ..................................................................................... 3 Monitoring symptoms, patient satisfaction, and health care performance ................................ 3 Example from the NIH Collaboratory ................................................................................................................... 4 Measuring PROs: Instruments, Item Banks, and Devices ....................................................... 5 PRO Instruments ............................................................................................................................................... 5 Item Banks........................................................................................................................................................... 8 Devices ................................................................................................................................................................. -
Survey Data Collection Using Complex Automated Questionnaires
From: AAAI Technical Report SS-03-04. Compilation copyright © 2003, AAAI (www.aaai.org). All rights reserved. Survey Data Collection Using Complex Automated Questionnaires William P. Mockovak, Ph.D. Bureau of Labor Statistics Office of Survey Methods Research 2 Massachusetts Ave. N.E. Washington, DC 20212 [email protected] Abstract Since the early 1980s, researchers in the federal statistical com- The CPS is conducted by a workforce of about 1,500 inter- munity have been moving complex surveys from paper question- viewers scattered across the U.S. who conduct interviews naires to computer-assisted interviewing (CAI). The data col- in respondents’ homes and, occasionally, on doorsteps, lected through such surveys cover a variety of needs, from critical porches, lawns, etc., or over the telephone from either an information on the health of the economy to social issues as interviewer’s home or from a centralized telephone inter- measured by statistics on health, crime, expenditures, and educa- viewing facility. Although the composition of the inter- tion. This paper covers some of the key issues involved in devel- viewer workforce has undergone some changes in recent oping applications used primarily by a middle-age, part-time years with the increased hiring of retirees, historically, the workforce, which uses the software in a variety of situations, majority of interviewers have been women between the while interacting with an occasionally uncooperative public. ages of 45 and 55, who work part-time, and who lack many of the computer skills taken for granted in younger popula- Introduction tions. Many interviewers tend to work on a single, primary survey, but are available to work on others (some continu- Government surveys provide critical information on a vari- ous, some one-time).