Maritime Health Research and Education-NET/Draft COST protocol

For the start of a COST-protocol

Title page

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  • Article title
  • Authors
  • Afiliaciones
  • Contact, name, mail, afiliacion

Abstract

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100-150 palabras

Problem to be solved
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Research questions
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Methods
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Expected results
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Introduction Background/rationale

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  • Explain the scientific background and rationale for the investigation being done

Objectives

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  • State the research questions, including any prespecified hypotheses

Methods

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Study design
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  • Present key elements of study design early in the paper
Setting
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  • Describe the setting, locations, and relevant dates, including periods of recruitment, exposure, follow-up, and data collection
Participants
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  • (a) Give the eligibility criteria, and the sources and methods of selection of participants
Variables
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  • Clearly define all outcomes, exposures, predictors, potential confounders, and effect modifiers. Give diagnostic criteria, if applicable
Data sources/ measurement
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  • For each variable of interest, give sources of data and details of methods of assessment (measurement). Describe comparability of assessment methods if there is more than one group
Bias
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  • Describe any efforts to address potential sources of bias
Study size
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  • Explain how the study size was arrived at
  • Quantitative variables
  • Explain how quantitative variables were handled in the analyses. If applicable, describe which groupings were chosen and why
Statistical methods
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  • a) Describe all statistical methods, including those used to control for confounding
  • (b) Describe any methods used to examine subgroups and interactions
  • (c) Explain how missing data were addressed
  • (d) If applicable, describe analytical methods taking account of sampling strategy
  • (e) Describe any sensitivity analyses
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The participants will be explained the purpose and details of the study through confirming the consent from the beginning of the questionnaire before the start. All of information from the participants will be confidential and only used for scientific purpose.

Ethical requirements

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The ethical rules for database research in Denmark and for the University of Southern Denmark are complied with. Confidentiality in handling personal information is done according to the rules set out by the Danish Data Protection Agency. There are no personal sensitive information included so approval from the Ethics Committee or written informed consent is not necessary. Data and results will be used for the public health master thesis in the University of Southern Denmark.

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The participants will be explained the purpose and details of the study through consent from the beginning of the questionnaire before the start. All of information from the participants will be confidential and only used for scientific purpose.

Chronogram
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Where and when will the data be collected

Dissemination of results
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Research team
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Financial budget
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References

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