4 results on '"Internal validity"'
Search Results
2. Comment le praticien doit-il interpréter les résultats d’un essai clinique ?
- Author
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E. Fakra, Raoul Belzeaux, D. Pringuey, T. Bottai, Marc Adida, Michel Cermolacce, Arthur Kaladjian, O. Blin, Nicolas Simon, Jean-Arthur Micoulaud-Franchi, J.-M. Azorin, Institut de Neurosciences des Systèmes (INS), and Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)
- Subjects
medicine.medical_specialty ,Psychotherapist ,[SCCO.NEUR]Cognitive science/Neuroscience ,Comparability ,030227 psychiatry ,law.invention ,External validity ,03 medical and health sciences ,Psychiatry and Mental health ,0302 clinical medicine ,Arts and Humanities (miscellaneous) ,Randomized controlled trial ,law ,Statistical significance ,Physical therapy ,medicine ,Clinical endpoint ,Internal validity ,Psychology ,030217 neurology & neurosurgery ,ComputingMilieux_MISCELLANEOUS - Abstract
To correctly interpret the results of a randomised controlled trial (RCT), practitioners have to spot bias and other potential problems present in the trial. Internal as well as external validity of the trial are linked to the presence of such bias. The internal validity is ensured by a clear definition of the objectives of the trial. The number of patients to be included in the trial is calculated on the basis of the main objective of the trial and more precisely on the basis of the primary endpoint selected to assess the efficacy of treatment. This is the best way to ensure that the statistical significance of the result may have a clinical relevance. Internal validity depends also on the process of patients selection, the methods used to ensure comparability of groups and treatments, the criteria employed to assess efficacy, and the methods for the analysis of data. External validity refers to subjects that have been excluded from the trial, limitations of RCTs, as well as the coherence and clinical relevance of the trial. Internal validity has to be fueled by external validity.
- Published
- 2016
- Full Text
- View/download PDF
3. Does the origin of olive oil influence the sensory perception ? Ask the control group
- Author
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Dekhili, Sihem, d'hauteville, François, European Science Foundation, ., Marchés, Organisations, Institutions et Stratégies d'Acteurs, Centre de Coopération Internationale en Recherche Agronomique pour le Développement (Cirad)-Institut National de la Recherche Agronomique (INRA)-Centre International de Hautes Etudes Agronomiques Méditerranéennes - Institut Agronomique Méditerranéen de Montpellier (CIHEAM-IAMM), Centre International de Hautes Études Agronomiques Méditerranéennes (CIHEAM)-Centre International de Hautes Études Agronomiques Méditerranéennes (CIHEAM)-Institut national d’études supérieures agronomiques de Montpellier (Montpellier SupAgro), Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro)-Institut national d'enseignement supérieur pour l'agriculture, l'alimentation et l'environnement (Institut Agro), and European Science Foundation (ESF)
- Subjects
PERCEIVED QUALITY ,VALIDITE INTERNE ,QUALITE PERCUE ,REGION OF ORIGIN ,QUASI-EXPERIMENTAL DESIGN ,STATISTICAL POWER ,SENSORY ANALYSIS ,REGION D'ORIGINE ,INTERNAL VALIDITY ,PUISSANCE STATISTIQUE ,PLAN QUASI-EXPERIMENTAL ,[SHS]Humanities and Social Sciences - Abstract
International audience; Many studies examining the effect of information on consumer food product evaluation use a pre-test/post-test quasi-experimental design. Generally, one group of subjects is placed in successive tasting situations. However, sensory peerceptions are not stable overtime, which may lead to internal validity and statistical power problems. A review of the literature develops the advantages of introducing of control groups for the detection of the effects of the information on consumers responses. An empirical study measuring the effect of the region of origin image on the perceived quality of olive oil illustrates the use of control groups and exposes the various statistical means that can used to limit the effect of external uncontrolled variables.; La plupart des études examinant l’effet de l’information sur l’évaluation d’un produit alimentaire chez les consommateurs utilisent un plan quasi-expérimental de type pré-test/post-test avec un seul groupe. Or l’évaluation par les sujets de leurs perceptions sensorielles est instable dans le temps, ce qui peut poser problème au niveau de la validité interne et de la puissance statistique des résultats expérimentaux. Le recours à un groupe témoin peut pallier cette insuffisance. Une revue de la littérature est proposée afin de mettre en avant l’importance des groupes témoins dans la détection de l’effet de l’information. Une étude empirique mesurant l’effet de l’image de la région d’origine sur la qualité perçue de l’huile d’olive illustre l’utilisation de groupes témoins et expose les différents moyens statistiques susceptibles d’éliminer l’effet des variables externes.
- Published
- 2007
4. [How may practitioners interpret the results of clinical trials?]
- Author
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Azorin JM, Adida M, Blin O, Simon N, Fakra E, Cermolacce M, Bottai T, Pringuey D, Micoulaud-Franchi JA, Belzeaux R, and Kaladjian A
- Subjects
- Bias, Humans, Internal-External Control, Physician's Role, Randomized Controlled Trials as Topic standards, Reproducibility of Results, Data Interpretation, Statistical, Physicians, Randomized Controlled Trials as Topic statistics & numerical data
- Abstract
To correctly interpret the results of a randomised controlled trial (RCT), practitioners have to spot bias and other potential problems present in the trial. Internal as well as external validity of the trial are linked to the presence of such bias. The internal validity is ensured by a clear definition of the objectives of the trial. The number of patients to be included in the trial is calculated on the basis of the main objective of the trial and more precisely on the basis of the primary endpoint selected to assess the efficacy of treatment. This is the best way to ensure that the statistical significance of the result may have a clinical relevance. Internal validity depends also on the process of patients selection, the methods used to ensure comparability of groups and treatments, the criteria employed to assess efficacy, and the methods for the analysis of data. External validity refers to subjects that have been excluded from the trial, limitations of RCTs, as well as the coherence and clinical relevance of the trial. Internal validity has to be fueled by external validity., (© L’Encéphale, Paris, 2016.)
- Published
- 2016
- Full Text
- View/download PDF
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