Format of Synopsis
Format of Synopsis
Before starting to work on Dissertation/Article, the FCPS trainee has to send a Synopsis to RTMC and get it
approved. The synopsis is a brief out line (about four A-4 size pages or 1000 words is the maximum limit) of your
future work.
TITLE: Should reflect the objectives of the study. It must be written after the whole synopsis has been written so
that it is a true representative of the plan (i.e. the synopsis).
INTRODUCTION: Should contain brief background of the selected topic. It must identify the importance of study,
its relevance and applicability of results. It must clearly state the purpose of the study.
OBJECTIVES: Objectives are statements of mentions. They inform the reader clearly what the researcher plans to
do in his/her work. The must identify the variables involved in research. Objective should start with an action verb
and be sufficiently specific, measurable, achievable, relevant and time bound (SMART).
OPERATIONAL DEFINITION: May be required in some synopses. It is definition of a term specifically telling
how it will be measured for e.g.:
1. Morbidity: this encompass a number of aspects viz. prolonged hospital stay, severe pain, immediate
complications, long term sequelac. A research must define how a vague term will be measured.
2. Efficacy: These can by measured
i. Time taken in relieve of symptoms which may be pain, fever cough heartburn etc.
ii. Taking into account number of side effects.
iii. Time taken for complete recovery student is requirement to specify how he/she will measure efficacy.
HYPOTHESIS: A hypothesis is a statement showing expected relation b/w 2 variables. A hypothesis is needed in
the following study designs:
i. All interventional studies
ii. Cohort
iii. Case control
iv. Comparative cross sectional.
DURATION OF STUDY: How long will the study take with dates.
SAMPLE SIZE: How many patients will be included. If there are groups how many per group?
SAMPLE SELECTION:
Inclusion criteria: on what bases will patients be inducted in the study.
Exclusion criteria: On what bases will patients be excluded from the study.
DATA COLLECTION PROCEDURE: A detailed account of how the researcher will perform research; how s/he
will measure the variable. It includes:
Identification of the study variables
Methods for collection of data
Data collection tools (proforma/questionnaire)
DATA ANALYSIS PROCEDURE: Relevant details naming software to be used, which descriptive statistics and
which test of significance if and when required, specifying variables where it will be applied.
REFERENCES:
In Vancouver style (for detail refer to page 132).