Series: Quasi-Experimental Study DesignsQuasi-experimental study designs series—paper 1: introduction: two historical lineages
Section snippets
Background
The quest to understand causal relationships permeates the history of health research [1], [2]. While the randomized controlled trial has become the mainstay for clinical efficacy and safety testing, quasi-experiments offer important alternatives and additional opportunities for causal inferences about health and health care. Quasi-experiments can generate effect size estimates that can come close in causal strength to those obtained in controlled trials because—like trials—they can control for
Historical origins of quasi-experiments
One very broad definition of an experiment is a study, in which a researcher intervenes in the “natural” processes, to establish the causal effects of a treatment—in contrast, a quasi-experiment can then be identified as any study, in which the causal effects of a treatment are established without a researcher's intervention. In different sciences, different types of experiments have developed, which can lead to strong causal inferences through complete control of confounding. In the laboratory
A series on quasi-experiments in health research
While the historical origins and developments of different quasi-experiments are highly varied, the designs share important similarities. These similarities—in potential uses, in strengths and limitations, in the processes that typically generate the necessary data, etc.—become apparent when quasi-experiments are discussed together as a category of study designs that is distinct from experiments, on the one hand, and “nonexperiments,” on the other hand. The distinctness as a category of study
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2023, Diabetes Research and Clinical PracticeCitation Excerpt :Whereas current observational studies contribute ample evidence of an existing association between IPT and improved health outcomes that complements that of RCTs, causal inference is limited by design [24]. Natural or quasi-experimental research designs are becoming increasingly popular as a means to overcome this limitation and evaluate causal effects of, e.g., health care policies or treatments using real-world, observational data [25,26]. Like the randomisation process in RCTs, the goal of such designs is to control for both observed and unobserved confounding under a potential outcomes framework by exploiting quasi-random variation in routinely collected data [25–27].
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2022, Journal of Clinical EpidemiologyCitation Excerpt :Based on the small number of pooled ID-focused IPD analyses and the lack of modern causal method implementation found in this systematic review, we recommend increased interdisciplinary collaborations between statistical methodologists and ID-focused researchers. We also suggest the development of guidance documents related to the implementation and reporting of causal methods in the analysis of pooled participant-level data from longitudinal observational ID-focused studies which could be similar to the guidance produced for a recent series on quasi-experimental methods in health [57–69]. This study did not require any ethical approval because we used only publicly available data.
Epidemiology and development economics two sides of the same coin in impact evaluation
2022, Journal of Clinical EpidemiologyCitation Excerpt :Evaluation studies conducted by economists frequently use quasi-experimental methods, although randomized trials have become accepted as the golden standard (R. Khandker, Gayatri B., & Hussain A., 2010). Methods used in economic studies such as instrumental variable models (IV), local average treatment effect models, regression discontinuity design are now starting to be considered by epidemiologists [9,10]. Interrupted-time series designs and cohort studies, which are used by epidemiologists, are practically absent in evaluations conducted by economists.
Adjusting mean arterial pressure alarms improves the time spent within blood pressure targets in patients with septic shock: A quasi-experimental study
2021, Australian Critical CareCitation Excerpt :Nurses were also unaware that MAP control was evaluated both before and after implementation of MAP alarms, limiting the risk of Hawthorne effect. Thus, the comparability of the two groups herein limits usual concerns regarding internal validity of quasi-experimental studies.17 Second, patients were still outside the prescribed target range a quarter of the time, which suggests that, at least in part, the dose of norepinephrine was not timely adjusted.
Trials embedded in cohorts, registries, and health care databases are gaining ground
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