CEDAR Value Sets Ontology Study file type is Adverse Events. Study file type is Assessment Results. Study file type is Case Report Form. A responsible party role played by a person responsible for the overall conduct of a study. Study file type is Concomitant Medications. Criterion_Category value set used by the ImmPort basic_study_design template (version 2.29). Study file type is Data Dictionary. Study file type is Demographics. Exclusion Criterion used to evaluate whether a subject is a candidate for exclusion in a study. Titration is done manually, by visual inspection Fully Manual Inclusion Criterion used to evaluate whether a subject is a candidate for inclusion in a study. An Intervention Longitudinal study involves repeated observations of the same variables over long periods of time during an intervention study. It is to Interventional study as Longitudinal is to Observational study. In an interventional study, the investigators give the research subjects a particular medicine or other intervention. Usually, they compare the treated subjects to subjects who receive no treatment or standard treatment. Then the researchers measure how the subjects' health changes. Study file type is Interventions. Study file type is Lab Test Results (e.g. CBC, chemistry, cytokine). A longitudinal study is a correlational research study that involves repeated observations of the same variables over long periods of time - often many decades. It is a type of observational study. Person employed by the sponsor or clinical research organization, who is responsible for determining that a clinical study is being conducted in accordance with the protocol. A monitor's duties may include, but are not limited to, helping to plan and initiate a trial, assessing the conduct of trial, assisting in data analysis, interpretation, and extrapolation. Monitor has medical authority for the checking data and documentation from the trial and for the evaluation of its safety aspects. An observational study draws inferences about the possible effect of a treatment on subjects, where the assignment of subjects into a treated group versus a control group is outside the control of the investigator. Existence of precipitate is automatically sensed via an optical sensor Optically Sensed A person having a Role that is some Other value not in CV Terms. Precipitate is sensed in some other way (not optical, pH, or manual) Other Detection Method A responsible party role played by a person responsible for the overall conduct of a study. Role_In_Study value set used by the ImmPort basic_study_design template (version 2.29). Someone (or something) that controls, directs, and organizes people, resources, or processes. Data associated with a study. For studies at a data curation level 0, this is the default setting for data linked to a study. Study_File_Type value set used by the ImmPort basic_study_design template (version 2.29). Study file type is Study Medication. Study Summary Description document. Study_Type value set used by the ImmPort basic_study_design template (version 2.29). These study types are adapted from Clinicaltrials.gov terms. A worker role authorized to make study-related decisions and carry out tasks related to the study; this role occurs during the study timeline. Study file type is Substance Use. The method of titration is not known. Unknown Precipitate is sensed by automatically detecting the change of pH of the sample pH-Meter Sensed CEDAR Value Sets Ontology