-
effectivehealthcare.ahrq.gov/sites/default/files/mcda-ijzerman.pdf
January 01, 2011 - Slide 7
Conjoint analysis
Each participant receives N choice sets.
-
effectivehealthcare.ahrq.gov/sites/default/files/product/pdf/methods-guide-inclusion-nonrandomized-studies.pdf
September 01, 2022 - RCTs often
have narrow participant eligibility criteria that exclude some subsets of the population, … longitudinal
Retrospective • May be useful
for rare
diseases or
newer
interventions
• Ease of
participant … They lack participant follow-up and therefore do not
allow inference regarding temporality of the association … The closer to 1, the stronger the probability that the participant would be in
the intervention group … ; likewise, the closer to 0, the stronger the probability the participant would
be in the control group
-
effectivehealthcare.ahrq.gov/sites/default/files/wysiwyg/pdf/methods-guide-inclusion-nonrandomized-studies.pdf
September 01, 2022 - RCTs often
have narrow participant eligibility criteria that exclude some subsets of the population, … longitudinal
Retrospective • May be useful
for rare
diseases or
newer
interventions
• Ease of
participant … They lack participant follow-up and therefore do not
allow inference regarding temporality of the association … The closer to 1, the stronger the probability that the participant would be in
the intervention group … ; likewise, the closer to 0, the stronger the probability the participant would
be in the control group
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/version-3-immunity-after-COVID-19-appendix-table-B-1.xlsx
January 24, 2022 - Imunodiagnostic Products;
developed at Centers for Disease Control
Only one sample for serology per participant … who tested positive for SARS-CoV-2 infection at South West London Pathology during the study period Participant … cohort May-September 2020 to January 25, 2021 ~6.75 months (27 weeks) NR HCW & other essential workers Participant … Switzerland Data of SARS-CoV-2 infections was extracted from a centralized state registry and linked to each participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/study-design-framework_research.pdf
March 01, 2012 - Other considerations:
Meta-analysis of individual participant data
Modeling
Additional systematic … Additional Considerations
Meta-analysis of individual participant data, modeling, and additional systematic … Meta-analysis of individual participant data (MIPD). … In a meta-analysis of individual
participant data (MIPD), data from existing studies are brought together … When individual participant
data are available, outcome and exposure definitions can be standardized
-
effectivehealthcare.ahrq.gov/sites/default/files/wysiwyg/white-paper-standardized-library.pdf
February 01, 2019 - Began discussing
key participant,
provider, and
disease
characteristics that
should be collected … Continued discussion
of participant,
provider, and
disease
characteristics. … Defining Participant, Provider, and Disease Characteristics
The first OMF domain describes characteristics … of the participant, disease, and provider that
are important for fully defining an outcome measure … For each of the five
clinical areas, the project team developed an initial list of participant, disease
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/dietary-supplements_research-protocol.pdf
December 15, 2010 - : inclusion/exclusion criteria, numbers enrolled and analyzed,
participant characteristics (age, … controlled
studies
Uncontrolled
experimental (for
KQ 5 only)
Selection Bias
Appropriateness of participant … mode of harms
collection (e.g., active or passive, standard
tool)
X X X
aAppropriateness of participant … Methodological diversity will be explored by adequacy of participant selection,
important confounding
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/appendix-table-B-1-observational-studies.xlsx
March 20, 2021 - Serology done using "locally validated assays" NR Possible reinfection defined as a positive cohort participant … with two PCR+ samples ≥90 days apart, or a positive cohort participant with a new PCR+ test at least
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/fiber-intake-protocol.pdf
August 15, 2023 - allocation concealment, and outcome assessor blinding are
all unclear (with the recognition that the participant … Each study will be described in summary and evidence tables presenting study design
features, study participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/chronic-urinary-retention_research-protocol.pdf
November 19, 2012 - control characteristics (intervention components, timing, frequency, duration); followup
duration; participant … bias for this topic and to foster consistency with the RCT risk-of-bias instrument likely
including participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/registry-of-patient-registries_research-2012-2_1.pdf
January 01, 2012 - • To increase awareness of the registry in order to improve investigator and, in some cases,
participant … information about
patient registries will be posted on the RoPR at registry inception, prior to the first participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/methods-guidance-reporting-bias_methods.pdf
November 01, 2013 - biologics and devices
regulated by the
FDAb
No later than 21 days after
enrollment of first
participant … sample
- Participant flow
- Primary and
secondary outcomes
- Certain agreements
regarding dissemination … The RePORT
database does not include variables indicating study registration or participant recruitment … FDA for trials involving investigational new
drugs
Study Results
- Participant Flow
- Baseline … Key Inclusion and
Exclusion Criteria Inclusion and exclusion criteria for participant selection, including
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/diabetes-behavior-programs_executive.pdf
September 11, 2015 - Achieving program acceptability as measured by
participant attrition rates?
Key Question 2. … effect
on diabetes-related health care utilization; and (c) program
acceptability as measured by participant … According
to our decision rules for assessing risk of bias, a low
risk of bias for participant and … Participant blinding in
this manner was rarely reported. … All The risk of bias from participant and personnel blinding was high in most trials.
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/prostate-cancer-therapies-protocol_amended110619.pdf
November 02, 2019 - and exclusion criteria,
intervention and control characteristics, sample size, follow-up duration, participant … bias of
eligible RCTs will be assessed using the Cochrane Risk of Bias Tool.14 Components
include participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/linking-evidence-reviews-methods_0.pdf
October 01, 2018 - ............................................................................................... 7
Participant … We also documented participant discussion and questions during the
cyberseminar itself. … Participant Survey Results
Of the nine participants surveyed, only three responded, despite receiving … Organizational Context
Evaluation Results
Evaluation of the Cyberseminar
Evaluation of the EPC Report
Participant
-
effectivehealthcare.ahrq.gov/sites/default/files/related_files/preterm-birth-terbutaline-pump_executive.pdf
September 01, 2011 - Nonrandomized trial 1 12
Prospective cohort 2 13,14
Retrospective cohort 7 15-21
Case series 2 22,23
Participant … and one RCT reported outcomes related
to the pump device.11,22,23 In a case series of 51 women,
one participant … Setting All studies were from the United States and participant data were acquired from a
national database … Bias: A systematic error, arising from participant
selection or outcome measurement that produces an
-
effectivehealthcare.ahrq.gov/sites/default/files/osteoarthritis-knee-update-executive-170505.pdf
May 01, 2017 - University Arthritis Index [WOMAC] pain measures), as
two tools used in the same study on the same participant … We rated applicability of
participant populations and interventions separately, as
described below. … The most prevalent limit to study quality was participant
blinding: Only 33 of 85 RCTs reported an attempt … sufficient numbers
of participants to enable prespecified subgroup analysis
according to important participant … of the trials included in our review
modified interventions based on an assessment of
individual participant
-
effectivehealthcare.ahrq.gov/sites/default/files/ebc-challenge-case-130621.pdf
June 01, 2013 - This
process facilitated participant-to-participant communication, and was maintained until the close
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/autism-update_research-protocol.pdf
September 20, 2013 - able to be abstracted from data in the papers
Data must be presented in the aggregate (vs. individual participant … We anticipate that these data will include those related to baseline
participant characteristics (age … This quality-
assessment approach considered factors related to study design, diagnostic approach, participant
-
effectivehealthcare.ahrq.gov/sites/default/files/pdf/breast-reconstruction-mastectomy-protocol.pdf
April 09, 2020 - Because
NRCSs, like RCTs, can be impacted by the lack of blinding and by participant loss to followup … single-group studies, we will use the items from the Cochrane Risk of Bias Tool28 that pertain to
issues of participant … systematic review will be described in summary and evidence tables
presenting study design features, study participant