Veidlapa Nr. M-3 (8)
Study Course Description

Writing a Research Protocol

Main Study Course Information

Course Code
CFUBK_090
Branch of Science
Clinical medicine
ECTS
3.00
Target Audience
Life Science
LQF
Level 7
Study Type And Form
Full-Time

Study Course Implementer

Course Supervisor
Structure Unit Manager
Structural Unit
Department of Human Physiology and Biochemistry
Contacts

Riga, 9 Kronvalda boulevard, svek@rsu.lv, +371 67338307

About Study Course

Objective

To provide an understanding of the content of a scientific research protocol in the healthcare sector, to develop skills in the independent writing of such a protocol.

Preliminary Knowledge

Bachelor's degree in health care science, basic knowledge in epidemiology.

Learning Outcomes

Knowledge

1.• Name the parts of the content for the scientific research protocol • Describe the need and nature of the scientific rationale for research • Explain the concept of the research goal and objectives • Name the research designs used in the health sector, their characteristics, advantages and disadvantages • List and explain the basic elements of research methodology • Formulate the safety principles to be observed in the study • Explain the idea and principles of publishing policy of the research results • Explain the nature of the research timeframe and risk management • Define the basic principles of research ethics.

Skills

1.• Select and systematise adequate sources of information to justify the need and nature of the research • Articulate a focused research goal and appropriate objectives to achieve it • Differentiate between types of research in the health sector according to their design • Describe in detail the research methodology and tools to be used • Establish a publicity plan and conditions for the research results • If necessary, draw up informed consent forms for research participants.

Competences

1.• Critically evaluate the information needed to support the research, depending on the data sources and data collection approaches • Anticipate and articulate potential risks during the course of the study and develop a plan to address them • Integrate the acquired knowledge to independently design a scientific research protocol in accordance with the principles recommended by international bodies.

Assessment

Individual work

Title
% from total grade
Grade
1.

Individual work

-
-
During the study course a written independent work, a research protocol, must be written and presented. In order to evaluate the quality of the study course as a whole, the student must fill out the study course evaluation questionnaire on the Student Portal.

Examination

Title
% from total grade
Grade
1.

Examination

-
-
During the course the research protocol will be developed and presented independently.
2.

Examination

-
-
The compliance of the developed independent work with the components of the research protocol and their conditions. Final test.

Study Course Theme Plan

FULL-TIME
Part 1
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Recommended content of the study protocol
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Research justification, references
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Research goal and objectives
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Research design
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Research methodology, safety considerations
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Data processing, quality assurance in the research, expected results
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Publication of research results and publication policy
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Timeframe, anticipated challenges, project management
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Ethical aspects, types of informed consent
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Budget, cooperation
  1. Lecture

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Practical work
  1. Class/Seminar

Modality
Location
Contact hours
On site
Auditorium
2

Topics

Presentation of independently accomplished work.
Total ECTS (Creditpoints):
3.00
Contact hours:
24 Academic Hours
Final Examination:
Exam (Written)

Bibliography

Required Reading

1.

Fathalla M. F., Fathalla M. M. F. A practical guide for health researchers. World Health Organization, Regional Office for the Eastern Mediterranean, 2004

Other Information Sources

1.

World Health Organization. Research policy. Recommended format for a Research Protocol. WHO, Geneva, 2015