Table of Contents
As a result of the Workshop's scenario presentations, the
audience will:
-
Understand how opportunities and
challenges in effectiveness and translational research
(related to the research questions, setting, availability
of resources, etc.) lead to a consideration of a variety
of research designs.
-
Recognize key tradeoffs between
alternative research designs.
-
Identify one or more useful research
designs for effectiveness and translational studies.

Dates and Location
Tuesday, May 4 –
Wednesday, May 5, 2004
The Workshop was held on the NIH Main Campus
in Bethesda, MD:
Building 31C, 6th Floor, Room 10

More than a year ago, a
CDC and NIH planning committee was formed to consider how to
organize a meeting to explore the strengths and weaknesses of
various research designs for effectiveness and translational
research in complex, multi-level community health
interventions. For the purposes of this initiative,
community is defined broadly and includes the health care
system and other sectors.
The diverse nature of the planning committee indicated that
there is a broad interest in research designs for complex
interventions. The initiative was co-sponsored by
the National Institutes of Health (NIH) and the Centers for
Disease Control and Prevention (CDC), with additional support
from the Agency for Healthcare Research and Quality (AHRQ),
and in conjunction with the Robert Wood Johnson Foundation.
Its long-term objectives are:
-
To build broad-based consensus as to the
strengths and limitations of experimental,
quasi-experimental, and natural experiment research
designs for studying complex interventions, programs, or
policies at the practice or community level.
-
To encourage an enhanced understanding of
the strengths and weaknesses of experimental,
quasi-experimental, and natural experiment research
designs in the evaluation and critique of intervention
research.
Toward these ends, the format
chosen for the invitational meeting was to create scenarios
for which experts will have constructed two favored
research designs, and during the meeting they discussed
their perception of trade-offs between these designs.
The scenarios define the research question plus the nature
of the intervention and its setting, target population,
cost, and outcome measures. The topics for the
scenarios are: 1) prevention of Type 2 diabetes, 2)
prevention of childhood obesity, 3) improving the
management of asthma, 4) promotion of physical activity,
5) prevention of alcohol purchase and use among
adolescents, and 6) tobacco control and cessation.
Four scenarios were presented on the first day and two were presented on the second day.
Ample
discussion time was planned involving, first, the members of each working
group, and second, the other meeting participants. There
was discussion time at the end of each scenario and at the
end of each day. With the help of our discussion
facilitator, Tom Chapel of CDC, we looked forward to an
exciting exchange of ideas. The objective of this meeting
was to have dialogue and to gather information regarding the
strengths and weaknesses of various research designs using these
scenarios as illustrative examples. The purpose was not to
select a design that is the "winner," but rather, to examine the
trade-offs involved in choosing one design over another and to
describe the situations in which a given design would be
preferable. Increasing our scientific knowledge about the
effects of complex interventions will require the use of a
variety of research designs. We hope that this workshop
contributed in a small way to these vital research endeavors.

DAY 1:
Tuesday, May 4, 2004
(Transcript
of Day 1)
| 7:00 am |
Registration and
Continental Breakfast
|
| 8:00 am |
"Setting the Stage"
Rationale for Conference, CDC Perspective
Lawrence Green, DrPH, Centers for Disease Control and
Prevention |
| |
|
| |
AHRQ Perspective
Denise Doughtery, PhD, Agency for Healthcare Research and
Quality |
| |
|
| |
NIH Perspective,
Description of the Pre-conference Process
Lawrence Fine, MD, DrPH, Office of Behavioral and Social
Sciences Research |
| |
|
| |
Logistics of the Day
Including Welcome Note, Scenario table, and Schedule
Thomas Chapel, MA, MBA, Centers for Disease Control and
Prevention |
| |
|
| 8:30 am |
Scenario 1:
Prevention
of Type 2 Diabetes
Marshall Chin, MD, Univeristy of Chicago
Carol Mangione, MD, MSPH, School of Medicine at UCLA |
| 9:50 am |
Break
|
| 10:05 am |
Scenario 2: Prevention
of Childhood Obesity
Steven L. Gortmaker, PhD, Harvard School of Public
Health
Robert W. Jeffrey, PhD, University of Minnesota
David M. Murray, PhD, University of Memphis |
| 11:25 am |
LUNCH
|
| 12:45 pm |
Commentator
Comment on Presentation & Discussion of Scenarios 1,
2 & International Perspective
Rob Sanson-Fisher, PhD, University of Newcastle,
Australia |
| 1:15 pm |
Scenario 3: Promotion of
Physical Activity
Ross C. Brownson, PhD, Saint Louis University of Public
Health
Deborah A. Cohen, MD, MPH, RAND Corporation
Henry A. Feldman, PhD, Children's Hospital Boston |
| 2:45 pm |
Break
|
| 3:00 pm |
Scenario 4: Tobacco
Control and Cessation Among Adolescents
(large presentation; takes longer to
load)
Anthony Biglan, PhD, Oregon Research Institute
K. Stephen Brown, PhD, University of Waterloo, Canada
Brian R. Flay, D.Phil, University of Illinois at Chicago |
| 4:30 pm |
Commentator
Comment on Presentations & Discussion of Scenarios
1-4
Thomas Cook, PhD, Northwestern University, Institute for
Policy Research
Discussion |
DAY 2: Wednesday, May 5, 2004 (Transcript
of Day 2)
|
7:30 am |
Continental
Breakfast
|
|
8:30 am |
Scenario 5:
Improving the Management of Asthma
Carlos Camargo, MD, DrPH, Harvard University
Sandra Wilson, PhD, Palo Alto Medical Foundation Research
Institute |
|
9:50 am |
Break
|
|
10:10 am |
Scenario 6:
Prevention of Alcohol Purchase and Use Among Adolescents
Ralph Hingson, ScD, MPH, National Institute on Alcohol
Abuse and Alcoholism
Harold Holder, PhD, Prevention Research Center
William R. Shadish, PhD, University of California, Merced |
|
11:30 am |
LUNCH
|
|
12:30 pm |
"Exploring the
Trade-offs"
Time Series
Henry Feldman, PhD, Children's Hospital Boston
Natural Experiment
Steven L. Gortmaker, PhD, Harvard School of Public Health
Group Randomized Trials
David M. Murray, PhD, University of Memphis
Staggered Enrollment
Marshall Chin, MD, University of Chicago
Regression Discontinuity
William R. Shadish, PhD, University of California, Merced
Multiple Baseline
Rob Sanson-Fisher, PhD, University of Newcastle, Australia |
|
2:00 pm |
"Reflections
and Next Steps"
Facilitated by Lawrence Green & Lawrence Fine
Mary Northridge, PhD, MPH, Columbia University
|

Anthony Biglan, PhD, Oregon Research Institute
(large
presentation; takes longer to load)
K. Stephen Brown,
PhD, University of Waterloo,
Canada
Ross C. Brownson, PhD, Saint Louis University School of Public
Health
Carlos A. Carmargo, MD, DrPH, Harvard University
Marshall H. Chin, MD, MPH, FACP, University of Chicago
Deborah A. Cohen, MD, MPH, RAND Corporation
Thomas D. Cook, PhD, Northwestern University
Henry A. Feldman, PhD, Children's Hospital Boston
Brian R. Flay, D.Phil, University of Illinois at Chicago
Steve Gortmaker, PhD, University of Wisconsin, Madison
Harold D. Holder, PhD, Prevention Research Center at the Univ.
of California, Berkeley
Robert W. Jeffery, PhD, University of Minnesota
Carol M. Mangione, MD, MSPH, University of California, Los
Angeles
David Murray, PhD, University of Memphis
Mary E. Northridge, PhD, MPH, Columbia University
Rob Sanson-Fisher, PhD, University of Newcastle Australia
William R. Shadish, MS, PhD, University of California, Merced
A compilation of
Speaker Bios is available electronically.

For additional information on the Research Designs for
Complex, Multi-level Health Interventions and Programs
Workshop, please contact Ms.
Dana Sampson via e-mail or phone at 301-402-1146.
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