Methodology series module 3: Cross-sectional studies

Cross-sectional study design is a type of observational study design. In a cross-sectional study, the investigator measures the outcome and the exposures in the study participants at the same time. Unlike in case-control studies (participants selected based on the outcome status) or cohort studies (...

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Vydáno v:Indian journal of dermatology Ročník 61; číslo 3; s. 261 - 264
Hlavní autor: Setia, Maninder
Médium: Journal Article
Jazyk:angličtina
Vydáno: India Wolters Kluwer - Medknow Publications 01.05.2016
Medknow Publications and Media Pvt. Ltd
Medknow Publications & Media Pvt. Ltd
Medknow Publications & Media Pvt Ltd
Wolters Kluwer Medknow Publications
Témata:
Acne
Acquired immune deficiency syndrome
AIDS
Antibiotics
Behavior
Confidence intervals
Cross-sectional studies
Dermatologists
design
Drug resistance
Epidemiology
Females
Health risk assessment
HIV
Human immunodeficiency virus
IJD
Infections
limitations
Males
Module on Biostatistics and Research Methodology for the Dermatologist - Module Editor: Saumya Panda
Polls & surveys
Population
Practice
RNA polymerase
Sociodemographics
strengths
Studies
Surveillance
Transgender persons
Trends
Vitiligo
Pennsylvania
India
Cross-sectional studies
strengths
design
limitations
ISSN:0019-5154, 1998-3611, 1998-3611
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Shrnutí:Cross-sectional study design is a type of observational study design. In a cross-sectional study, the investigator measures the outcome and the exposures in the study participants at the same time. Unlike in case-control studies (participants selected based on the outcome status) or cohort studies (participants selected based on the exposure status), the participants in a cross-sectional study are just selected based on the inclusion and exclusion criteria set for the study. Once the participants have been selected for the study, the investigator follows the study to assess the exposure and the outcomes. Cross-sectional designs are used for population-based surveys and to assess the prevalence of diseases in clinic-based samples. These studies can usually be conducted relatively faster and are inexpensive. They may be conducted either before planning a cohort study or a baseline in a cohort study. These types of designs will give us information about the prevalence of outcomes or exposures; this information will be useful for designing the cohort study. However, since this is a 1-time measurement of exposure and outcome, it is difficult to derive causal relationships from cross-sectional analysis. We can estimate the prevalence of disease in cross-sectional studies. Furthermore, we will also be able to estimate the odds ratios to study the association between exposure and the outcomes in this design.
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ISSN:0019-5154
1998-3611
1998-3611
DOI:10.4103/0019-5154.182410