Admission requirements
Mandatory course for Master students with specialisation Clinical Psychology.
Description
Clinical psychological research is often concerned with investigating the causes of abnormal behavior or with its treatment. A range of study designs can used to identify causes of illness, both cross-sectional and longitudinal designs. Treatment evaluation designs range from case reports to randomized clinical trials (RCTs). RCTs have rapidly become the gold standard of evidence in biomedical research. However, the vast majority of studies is observational. Furthermore, it has been argued that RCTs are impractical in some circumstances, and impossible in others.
In this course we will discuss the strengths and weaknesses of cohort-studies, case-control studies and cross-sectional studies for investigating causal relationships. Secondly, we will discuss the strengths and weaknesses of different treatment evaluation designs, as well as the standards of conducting and reporting this research. Recent developments in psychotherapy and psychopharmacology research will be used as examples.
Course objectives
Learn to reflect upon the strengths and weaknesses of research designs typically used in clinical psychology.
Learn to assess research papers on the merits of their chosen research strategies and design.
Learn the standards of reporting of various types of clinical research, including the rationale for these standards.
Gain knowledge about recent developments in psychological treatments of psychiatric disorders.
Timetable
Experimental Clinical Psychology (2014-2015):
Lectures (1st semester)
Workgroups (1st semester)
Lectures (2nd semester)
Workgroups (2nd semester)
Exams (2nd semester)
Mode of instruction
Six two hour lectures and six two hour seminars, 100% attendance is required.
Registration
Course
Students need to enroll for lectures and work group sessions. Please consult the Instructions on registration
Examination
Students are not automatically enrolled for an examination. They need to register via uSis from 100 to 10 calendar days before the date of the exam; students who are not registered will not be permitted to take the examination. Registering for exams
Assessment method
6 graded assignments (40%)
grade for participation during seminars, including presentation of assignment (15%)
final exam (essay questions) (45%)
The Faculty of Social Sciences has instituted that instructors use a software programme for the systematic detection of plagiarism in students’ written work. In case of fraud disciplinary actions will be taken. Please see the information concerning fraud
Blackboard
Information on blackboard.leidenuniv.nl
Reading list
- Kazdin, Alan E.(2009) Research Design In Clinical Psychology. 524 pagina’s, Pearson Education (US) | International ed of 4th revised ed juni 2009 ISBN13 9780205774067 Paperback (NB: make sure you buy the paperback (appr. 42 euro instead of 140)
Furthermore, the following papers will be made available through Blackboard.
Vandenbroucke JP (2008). Observational research, randomized trials, and two views of medical science. PLoS Medicine 5: e67.
Vandenbroucke JP et al. (2007). Strengthening the Reporting of Observational Studies in Epidemiology (STROBE): Explanation and elaboration. PLoS Medicine 4: e297.
Altman DG et al. (2001). The revised CONSORT statement for reporting randomized trials: Explanation and elaboration. Annals of Internal Medicine 134: 663-694.
Boutron I et al. (2008). Extending the CONSORT statement to randomized trials of nonpharmacological treatment: explanation and elaboration. Annals of Internal Medicine 148: 295-309.
Contact information
Prof.dr. Willem van der Does
Room 2 B33
Tel. +31 (0)71 527 8482
Email: vanderdoes@fsw.leidenuniv.nl