course-details-portlet

KLMED8009 - Klinisk forskning

Om emnet

Vurderingsordning

Vurderingsordning: Skriftlig skoleeksamen
Karakter: Bestått/ Ikke bestått

Vurdering Vekting Varighet Delkarakter Hjelpemidler
Skriftlig skoleeksamen 100/100 4 timer D

Faglig innhold

The course consists of three parts, 3 + 2 + 2 days, usually in the beginning of September, October and November. The course is focusing on Randomized Controlled Trials (RCTs) and will cover all the important aspects of RCTs, from design to reporting. Particular emphasis will also be placed upon practical aspects. Recent advances in RCT methodology will be covered. Other research designs will also be presented with focus on strengths and limitations. Protocol design will be covered with focus on background, eligibility criteria, randomization, sample size, outcome measures, procedures for participants, monitoring, reporting and analysis, and publication policy. A short introduction/repetition of basic statistics will focus on significance tests, confidence intervals, p-values and sample size estimation. Fraud, bias and confounding will be discussed. The course also covers the use of clinical measurements and studies on diagnostic tests, including precision, accuracy, validity, specificity, sensitivity, reproducibility, feasibility, appropriateness and how to interpret the results in a clinical setting. Further, the course will focus on Patient Reported Outcomes (PRO). Worldwide there is an increasing demand to always consider measurements of PRO in new clinical trials. Measurements of PRO and subjective symptoms are generally important, but particularly important in studies of palliative care. The course will cover several aspects of these measurements in randomized studies and clinical trials; choice of questionnaire, methods, study design, problem solving, analysis and comprehension of the data, report of results and conclusions. The course will also focus on how to read and interpret papers with focus on how to evaluate the scientific quality, i.e. should the results be trusted or not. An important part of this is homework with a written evaluation of selected papers. Having taken the course participants should be able to evaluate the work of others as well as to plan, execute and report their own clinical studies according the highest scientific standards.

Læringsutbytte

After completing the course, the student is:

  • able to assess the expediency and application of the different designs in clinical research including more sophisticated designs
  • able to contribute to the improvement of designs and methods in clinical research
  • by a given hypothesis able to formulate research questions in accordance with the different types of design
  • with the correct methods able to design, implement, analyze and publish clinical research on an international level
  • able to identify research questions related to design and carry out research with a methodical integrity
  • able to communicate clinical research and development through acknowledged national and international channels
  • able to select and use methods of patient reported outcome
  • able to use methods for relevant literature search
  • able to evaluate the quality of clinical research papers according to research methods used controlled clinical experiment.

Læringsformer og aktiviteter

Lectures, group work, home assignment. To be allowed to take the examination all homework must be delivered on time and at least 80% attendance of the lectures is mandatory.

Obligatoriske aktiviteter

  • Gjennomføre oppgave mellom samlingene og eksamen
  • Alle forelesninger/samlinger

Mer om vurdering

If retake of the examination this can be either by a written or an oral test. This is to be deceided by the person responsible for the course.

Spesielle vilkår

Obligatorisk aktivitet fra tidligere semester kan godkjennes av instituttet.

Forkunnskapskrav

Master degree or similar. Medical students at The Student Research Programme. Candidates with a lower degree will be assessed individually.

Kursmateriell

Stephen B Hulley et al. Designing Clinical Research (fourth edition) Forlag: Lippincott Williams & Wilkins: 2013. ISBN: 978-1-60831-804-9. David Machin & Peter Fayers. Randomized controlled trials. Design, practice and reporting. Forlag: Wiley-Blackwell 2009/2010. ISBN-10: 0471498122. ISBN-13: 978-0471498124.

Studiepoengreduksjon

Emnekode Reduksjon Fra Til
KLMED8003 4.0 HØST 2012
KLMED8007 5.0 HØST 2012
Flere sider om emnet

Ingen

Fakta om emnet

Versjon: 1
Studiepoeng:  7.5 SP
Studienivå: Doktorgrads nivå

Undervisning

Termin nr.: 1
Undervises:  HØST 2021

Undervisningsspråk: Engelsk

Sted: Trondheim

Fagområde(r)
  • Klinisk medisin
  • Medisin
Kontaktinformasjon
Emneansvarlig/koordinator:

Ansvarlig enhet
Institutt for klinisk og molekylær medisin

Eksamensinfo

Vurderingsordning: Skriftlig skoleeksamen

Termin Statuskode Vurdering Vekting Hjelpemidler Dato Tid Eksamens- system Rom *
Høst ORD Skriftlig skoleeksamen 100/100 D 13.12.2021 15:00
Rom Bygning Antall kandidater
SL510 Sluppenvegen 14 24

Vurderingsordning: Muntlig

Termin Statuskode Vurdering Vekting Hjelpemidler Dato Tid Eksamens- system Rom *
Vår UTS Muntlig 100/100 01.04.2022 09:00
Rom Bygning Antall kandidater
SL310 blå sone Sluppenvegen 14 1
  • * Skriftlig eksamen plasseres på rom 3 dager før eksamensdato. Hvis mer enn ett rom er oppgitt, finner du ditt rom på Studentweb.
Eksamensinfo

For mer info om oppmelding til og gjennomføring av eksamen, se "Innsida - Eksamen"

Mer om eksamen ved NTNU