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Intervention group The group receiving the study agent that is being tested in a clinical trial or clinical study. (NCI) Intervention name The generic name of the precise intervention being studied. (NLM) Intra-rater reliability The property of yielding equivalent results when used by the same rater on different occasions. (ICH E9) Investigational
ITT analysis is intended to avoid various misleading artifacts that can arise in intervention research such as non-random attrition of participants from the study or crossover. ITT is also simpler than other forms of study design and analysis, because it does not require observation of compliance status for units assigned to different ...
Phase IV is post-approval studies. [8] Phase I includes 20 to 100 healthy volunteers or individuals with the disease or condition. [1] [3] This study typically lasts several months and its purpose is to prove safety and an effective dosage. Phase II includes a larger number of individual participants in the range of 100–300, and Phase III ...
The first line of treatment for hypertension is lifestyle changes, including dietary changes, physical exercise, and weight loss. Although these have all been recommended in scientific advisories, [7] a Cochrane systematic review of available relevant studies found that although weigh-loss diets did reduce body weight and blood pressure, beneficial effects of those changes could not be ...
A quasi-experiment is an empirical interventional study used to estimate the causal impact of an intervention on target population without random assignment.Quasi-experimental research shares similarities with the traditional experimental design or randomized controlled trial, but it specifically lacks the element of random assignment to treatment or control.
IDEAL (Idea, Development, Exploration, Assessment, Long-term study) is a framework for describing the stages of innovation in surgery and other interventional procedures.. The purpose of IDEAL is to improve the quality of research in surgery by emphasizing appropriate methods, transparency of data and rigorous reporting of outcom
A megastudy or mega-study is a research study in which a large number of different treatments or interventions are tested at the same time, on the same sample or similar samples, using a common outcome measure, and using the same experimental protocol. [1] [2] [3] This research design ensures the outcomes across interventions are comparable.
One significant issue with parallel studies, though, is the concept of intra subject variability, which is defined as variability in response occurring within the same patient. [1] The two treatment groups in a parallel study can either consist of two completely separate treatments (i.e. different drugs), or simply different doses of a common drug.