Scientific Research
The Fountain of
Knowledge
Professor Syed Amin Tabish
FRCP (London), FRCP (Edin.), FAMS, MD (AIIMS)
Postdoc Fellowship, Bristol University (England)
Doctorate in Educational Leadership (USA)
Scientific Research
 Research conducted for the purpose of
contributing towards science by the
systematic collection, interpretation and
evaluation of data and that, too, in a
planned manner is called scientific
research
It is a systematic collection, analysis and
interpretation of data to answer a question
or solve a problem
Classification of Scientific Research
 According to data collection techniques:
 Observational
 Experimental
 According to causality relationships:
 Descriptive
 Analytical
 According to relationships with time:
 Retrospective
 Prospective
 Cross-sectional
Classification of Scientific Research
According to the medium through
which they are applied:
Clinical
Laboratory
Social descriptive research
Classification Of Research
I. Descriptive research
 Case series
 Surveillance studies
II. Analytical research
 Observational studies: cohort, case control and cross-
sectional research
 Interventional research: quasi-experimental and clinical
research
Analytical observational research
OBSERVATIONAL
 Cohort Studies (Prospective, Retrospective and
Ambidirectional)
 Case-Control studies
 Cross-Sectional studies
INTERVENTIONAL RESEARCH (Experimental
Studies)
1. Quasi-Experimental Research
2. Clinical Research
Quantitative Research
 It is numerical, non-descriptive, applies statistics
or mathematics, and uses numbers.
 It is an iterative process whereby evidence is
evaluated.
 The results are often presented in tables and
graphs.
 It is conclusive.
 It investigates the what, where, and when of
decision-making.
Qualitative Research
 It is non-numerical, descriptive, applies to
reason, and uses words.
 Its aim is to get the meaning, and feeling and
describe the situation.
 Qualitative data cannot be graphed.
 It is exploratory.
 It investigates the why and how of decision-
making
Types of Questions
Academic “Basic”
 To add to our scientific
knowledge
Applied “Practical”
 To solve our practical
problems
Research: the Fountain of Knowledge
 A research problem refers to a difficulty that a researcher or
a scientific community or an industry or a government
organization or a society experiences. It may be a theoretical
or a practical situation. It calls for a thorough understanding
and possible solutions.
 Research provides the basis for many government policies.
For example, research on the needs and desires of the
people and on the availability of revenues to meet the needs
helps a government to prepare a budget.
 It is the fountain of knowledge and provides guidelines for
solving problems.
Step 1. Define a Research Area
Areas for
research are
very broad
and
overlapping
Selection depends on
Researcher’s
interest
Actual need
Available resource
1. RESEARCH AREA
Cardiology
Step 2: Select a Research Topic
Researcher can
not study every
topic in the
selected area
Magnitude of
problem
Seriousness
Preventability
Curability
Feasibility
2. RESEACH TOPIC
Ischemic Heart Diseases
Step 3. State the Research
Objectives?
 State objectives at
the beginning of
study
 State them clearly
 Objectives are stated
in two forms
Goal (general
objectives)
Specific objectives
Research Objectives Should Be
 Closely related to research questions
 Covering all aspects of the problem
 Very specific
 Ordered in logical sequence
 Achievable (take in account time & resource)
 Mutually exclusive (no repetition, no overlaps)
 Stated in action verb that can be evaluated
3. GOAL (GENERAL
OBJECTIVES)
To contribute to prevention
of Ischemic Heart Disease
PRIMARY OBJECTIVES
To determine the effect of reducing
serum cholesterol (LDL) on the
occurrence of MI
SECONDARY OBJECTIVES
To describe the side effects of
lowering serum cholesterol
Step 4. Develop a Research
Question
 Before start, you make sure that
You has a research question
Question is clear and specific
Reflect the objective (s)
Has no answer by common sense
Has no answer in literature
Finding an answer will solve the problem of
the study
At this stage, review of
literature is very
important to ensure that
research question has
no answer
Review of literature is important
 Identify valid question
 Refine question(s)
 Avoid un-needed research
 Avoid duplication
 Avoid pitfalls of previous studies
 Provide scientific background
 Give rationale for study
Examples of Questions (1)
Description
 What is the incidence
of disease “D”?
 What is the prevalence
of disease “D”?
 What is the rate of
risk factor “F” in the
community?
Examples of Questions (2)
Etiology
 What is the cause of
disease “D”?
 Is exposure “E”
associated with disease
“D”?
 What is the risk factor
“F” associated with
the disease “D”?
Examples of Questions (3)
Diagnosis
 Is test “T1” better
than test “T2” in
diagnosis disease “D”?
 What the value of test
“T” in diagnosis
disease “D”?
Examples of Questions (4)
Therapy
 Is drug “A” better
than drug “B” in
treatment of disease
“D”?
 Is surgery more
effective than
conservative
treatment for disease
“D”?
Examples of Questions (5)
Prognosis
 What is the five-year
survival of patients
with disease “D”?
 What is the five-year
survival of patients
having disease “D”
after intervention “I”?
4. RESEARCH QUESTION
Does hypo-cholesterolemic agent
“A” decrease the risk of MI ?
Step 5: Formulate a Hypothesis
It is a statement
of research
question in a
measurable
format
Hypothesis; must be:
 Based on scientific
background
 Translation of research
question
 Reflect the study design
 Use the study variable
 Test only one relationship
 Stated in measurable terms
Example for Formulating a Sound
Hypothesis
A prospective cohort study was designed
to answer the research question: “ is
hypercholesterolemia (HC) a risk factor
for coronary artery disease (CAD)?”
Examine the Following
Hypothesis
1. All subjects having HC will develop CAD
2. Dietary habits affect the risk of CAD
3. Rats given high fat diet will develop CAD
4. Atherosclerosis is associated with a high risk of
CAD
5. Increased serum cholesterol and triglycerides
and decreased HDL lead to increased risk f
CAD
6. CAD is high among hypercholesterolemic
subjects
7. Subjects with HC have a higher risk of
developing CAD compared to subjects without
HC
8. The prevalence of CAD among HC subjects is
higher than that in subjects without HC
9. The probability of HC in CAD patients is
higher than in subjects without CAD
 Hypothesis (1) is refuted because it is not biologically
plausible
 Hypothesis (2) is refuted because it is not related to
research question
 Hypothesis (3) is refuted because it does not reflect the
study design (cohort not experiment)
 Hypothesis (4) is refuted because it does not use the
study variables
 Hypothesis (5) is refuted because it examine more than
one relationship. It is better to use separate hypothesis
for each studied association
 Hypothesis (6) can be refuted because it is
not stated in a measurable terms.
Expression “high” is very subjective
 Hypothesis (8) & (9) an be refuted because
they do not reflect the study design.
Although they fulfill all other criteria
 Hypothesis (7) is a sound hypothesis
5. RESEARCH
HYPOTHESIS
Subjects with HC have a higher risk
of developing CAD compared to
subjects without HC
STUDY DESIGNS
 Classification
depends on role of
investigator in
controlling factors
under study
 Observational
 Ecological
 Cross sectional
 Case control
 Cohort
 Experimental/interven
tion
 Lab experiments
 Clinical trials
 Community interventions
 Quasi-experimental
1. Ecological Study
 Sampling units are
groups
 Good source for
new hypothesis
 Problems
Ecological fallacy
Temporal
relationship
2. Cross Sectional Study
 Data collected at a
single point in time
 No control group
 Prevalence rate can be
calculated
 Develop new
hypothesis
“Snapshot”
Prevalence vs. Incidence
 Prevalence
The total number of
cases at a point in
time
 Includes both new
and old cases
 Incidence
The number of new
cases over time
Example of a Cross-Sectional
Study
Study of association between garlic
consumption & CAD in the Family
Practice Clinic
Cross-sectional Study
Sample of Population
Garlic Eaters Non-Garlic Eaters
Prevalence of CAD Prevalence of CAD
Time Frame = Present
Cross-sectional Study
Garlic Consumption
+ -
C
A
D
+
- 90
10 90
10
Cross-Sectional Study
 Strengths
Quick
Cheap
 Weaknesses
 Weak evidence of
association
 Lack of
representativeness
 Absence of temporal
relationship
 No control of
confounders
 Prevalence-incidence
bias
3. Case-Control Study
 Start with people who have disease
 Compare them with controls that do
not
 Look back and assess exposures
Case-Control Study
Patients with CAD
Patients w/o CAD
Present
Past
High Garlic Diet
High Garlic Diet
Low Garlic Diet
Low Garlic Diet
Cases
Controls
Do not eat
Eat garlic
ill not ill
49 49 98
4 6 10
Presentation of Case-control Study
Strengths
 Good for rare outcomes: cancer
 Can examine many exposures
 Useful to test hypothesis
 Fast & easy
 Cheap
 Provides Odds Ratio
 Minimal ethical problems
 No risk to participants
 No attrition problems
Weaknesses
 Cannot measure
 Incidence
 Prevalence
 Relative Risk
 High susceptibility to
bias
Misclassification
bias
Recall bias
Selection bias
Confounding bias
Temporal
relationship
Exposed
Unexposed
Source
population
Cases
Exposed
Unexposed
Source population
Cases
Exposed
Unexposed
Source population
Sample
Intuitively
If the frequency of exposure is higher
among cases than controls
Then the incidence rate will probably be
higher among exposed than non
exposed.
Case Control Study
Disease
Controls
Exposure
?
?
Retrospective nature
Marching towards outcomes
Cohort Studies
Cohort Study
 Begin with disease-free individuals
 Classify individuals as exposed/unexposed
 Record outcomes in both groups
 Compare outcomes using relative risk
follow-up period
Calculate
measure of frequency:
 Cumulative incidence
- Incidence
- Attack rate (outbreak)
end of follow-up
Unexposed
Exposed
Cohort Studies
Unexposed
Exposed
Incidence among
exposed
Incidence among
unexposed
Cohort Studies
Example of a Cohort Study
To see the effects of smoking on lung
cancer development
Prospective Cohort Study
Non-smoker
Smoker
No
cancer
cancer
cancer
No
cancer
Present Future
Smokers
Non-smokers
ill not ill
70 6930 7000
3 2997 3000
Presentation of Cohort Data
Data Analysis
Incidence rate
 Among smokers =
70/7000=10/1000
 Among non-smoker =
3/3000 = 1/1000
Relative risk =
10/1 = 10
time
Exposure Study starts
Disease
occurrence
Prospective Cohort Study
Exposure
Disease
occurrence
time
Study starts
Retrospective Cohort Study
Exposure
time
Disease
occurrence Study starts
Strengths
 Provides incidence data
 Establishes time sequence for causality
 Eliminates recall bias
 Suitable for rare exposure
 Allows for accurate measurement of
exposure variables
Strengths
 Can measure multiple outcomes
 Can adjust for confounding variables
 Can calculate relative risk
Dose response can be calculated
Weaknesses
 Expensive
 Time consuming
 Problems of attrition
 Cannot study rare outcomes (diseases)
 Some ethical problems
Weaknesses
 Exposure may change over time
 Disease may have a long pre-clinical phase
 Change of diagnostic criteria
Experimental Studies
Clinical trials provide the “gold
standard” of determining the
relationship between garlic and
cardiovascular disease prevention.
Clinical Trials
 Randomized
 Double-blind
 Placebo-controlled
Clinical Trial
Study
Population
Treatment
Group
Control Group
Outcomes
Outcomes
R
a
n
d
o
m
i
z
e
Clinical Trial
Study
Population
R
a
n
d
o
m
i
z
e
Garlic Pill
Placebo
CAD
No CAD
CAD
No CAD
Strengths
 Best measure of causal relationship
 Best design for controlling bias
 Can measure multiple outcomes
Weaknesses
 Ethical issues
 Unawareness of patients
 Withholding beneficial treatment
 Inability to refuse (prisoners)
 Potential side effects
 Co-intervention & contamination
 Feasibility problems
Small Group Tasks
 Elect a leader and a speaker
 Read your scenario
 Design a study to answer the research question
 Your funds are not unlimited!
 Briefly present your study to the large group
 Time:
 10 min for study design
 10 min for group presentations
Selection of Research Design
 Selection of the best
research design
depends on many
factors
 Purpose of study
 State of existing
knowledge
 Characteristics of study
variables
(exposure/outcome)
 Latency
 Feasibility
Research: The Fountain of Knowledge
 A research problem refers to a difficulty that a
researcher or a scientific community or an industry or a
government organization or a society experiences. It
may be a theoretical or a practical situation. It calls for
a thorough understanding and possible solutions.
 Research provides the basis for many government
policies. For example, research on the needs and
desires of the people and on the availability of revenues
to meet the needs helps a government to prepare a
budget.
 It is the fountain of knowledge and provides guidelines
for solving problems.

Scientific Research

  • 1.
    Scientific Research The Fountainof Knowledge Professor Syed Amin Tabish FRCP (London), FRCP (Edin.), FAMS, MD (AIIMS) Postdoc Fellowship, Bristol University (England) Doctorate in Educational Leadership (USA)
  • 2.
    Scientific Research  Researchconducted for the purpose of contributing towards science by the systematic collection, interpretation and evaluation of data and that, too, in a planned manner is called scientific research It is a systematic collection, analysis and interpretation of data to answer a question or solve a problem
  • 3.
    Classification of ScientificResearch  According to data collection techniques:  Observational  Experimental  According to causality relationships:  Descriptive  Analytical  According to relationships with time:  Retrospective  Prospective  Cross-sectional
  • 4.
    Classification of ScientificResearch According to the medium through which they are applied: Clinical Laboratory Social descriptive research
  • 5.
    Classification Of Research I.Descriptive research  Case series  Surveillance studies II. Analytical research  Observational studies: cohort, case control and cross- sectional research  Interventional research: quasi-experimental and clinical research
  • 6.
    Analytical observational research OBSERVATIONAL Cohort Studies (Prospective, Retrospective and Ambidirectional)  Case-Control studies  Cross-Sectional studies INTERVENTIONAL RESEARCH (Experimental Studies) 1. Quasi-Experimental Research 2. Clinical Research
  • 7.
    Quantitative Research  Itis numerical, non-descriptive, applies statistics or mathematics, and uses numbers.  It is an iterative process whereby evidence is evaluated.  The results are often presented in tables and graphs.  It is conclusive.  It investigates the what, where, and when of decision-making.
  • 8.
    Qualitative Research  Itis non-numerical, descriptive, applies to reason, and uses words.  Its aim is to get the meaning, and feeling and describe the situation.  Qualitative data cannot be graphed.  It is exploratory.  It investigates the why and how of decision- making
  • 9.
    Types of Questions Academic“Basic”  To add to our scientific knowledge Applied “Practical”  To solve our practical problems
  • 10.
    Research: the Fountainof Knowledge  A research problem refers to a difficulty that a researcher or a scientific community or an industry or a government organization or a society experiences. It may be a theoretical or a practical situation. It calls for a thorough understanding and possible solutions.  Research provides the basis for many government policies. For example, research on the needs and desires of the people and on the availability of revenues to meet the needs helps a government to prepare a budget.  It is the fountain of knowledge and provides guidelines for solving problems.
  • 11.
    Step 1. Definea Research Area Areas for research are very broad and overlapping Selection depends on Researcher’s interest Actual need Available resource
  • 12.
  • 13.
    Step 2: Selecta Research Topic Researcher can not study every topic in the selected area Magnitude of problem Seriousness Preventability Curability Feasibility
  • 14.
  • 15.
    Step 3. Statethe Research Objectives?  State objectives at the beginning of study  State them clearly  Objectives are stated in two forms Goal (general objectives) Specific objectives
  • 16.
    Research Objectives ShouldBe  Closely related to research questions  Covering all aspects of the problem  Very specific  Ordered in logical sequence  Achievable (take in account time & resource)  Mutually exclusive (no repetition, no overlaps)  Stated in action verb that can be evaluated
  • 17.
    3. GOAL (GENERAL OBJECTIVES) Tocontribute to prevention of Ischemic Heart Disease
  • 18.
    PRIMARY OBJECTIVES To determinethe effect of reducing serum cholesterol (LDL) on the occurrence of MI
  • 19.
    SECONDARY OBJECTIVES To describethe side effects of lowering serum cholesterol
  • 20.
    Step 4. Developa Research Question  Before start, you make sure that You has a research question Question is clear and specific Reflect the objective (s) Has no answer by common sense Has no answer in literature Finding an answer will solve the problem of the study
  • 21.
    At this stage,review of literature is very important to ensure that research question has no answer
  • 22.
    Review of literatureis important  Identify valid question  Refine question(s)  Avoid un-needed research  Avoid duplication  Avoid pitfalls of previous studies  Provide scientific background  Give rationale for study
  • 23.
    Examples of Questions(1) Description  What is the incidence of disease “D”?  What is the prevalence of disease “D”?  What is the rate of risk factor “F” in the community?
  • 24.
    Examples of Questions(2) Etiology  What is the cause of disease “D”?  Is exposure “E” associated with disease “D”?  What is the risk factor “F” associated with the disease “D”?
  • 25.
    Examples of Questions(3) Diagnosis  Is test “T1” better than test “T2” in diagnosis disease “D”?  What the value of test “T” in diagnosis disease “D”?
  • 26.
    Examples of Questions(4) Therapy  Is drug “A” better than drug “B” in treatment of disease “D”?  Is surgery more effective than conservative treatment for disease “D”?
  • 27.
    Examples of Questions(5) Prognosis  What is the five-year survival of patients with disease “D”?  What is the five-year survival of patients having disease “D” after intervention “I”?
  • 28.
    4. RESEARCH QUESTION Doeshypo-cholesterolemic agent “A” decrease the risk of MI ?
  • 29.
    Step 5: Formulatea Hypothesis It is a statement of research question in a measurable format Hypothesis; must be:  Based on scientific background  Translation of research question  Reflect the study design  Use the study variable  Test only one relationship  Stated in measurable terms
  • 30.
    Example for Formulatinga Sound Hypothesis A prospective cohort study was designed to answer the research question: “ is hypercholesterolemia (HC) a risk factor for coronary artery disease (CAD)?”
  • 31.
    Examine the Following Hypothesis 1.All subjects having HC will develop CAD 2. Dietary habits affect the risk of CAD 3. Rats given high fat diet will develop CAD 4. Atherosclerosis is associated with a high risk of CAD 5. Increased serum cholesterol and triglycerides and decreased HDL lead to increased risk f CAD
  • 32.
    6. CAD ishigh among hypercholesterolemic subjects 7. Subjects with HC have a higher risk of developing CAD compared to subjects without HC 8. The prevalence of CAD among HC subjects is higher than that in subjects without HC 9. The probability of HC in CAD patients is higher than in subjects without CAD
  • 33.
     Hypothesis (1)is refuted because it is not biologically plausible  Hypothesis (2) is refuted because it is not related to research question  Hypothesis (3) is refuted because it does not reflect the study design (cohort not experiment)  Hypothesis (4) is refuted because it does not use the study variables  Hypothesis (5) is refuted because it examine more than one relationship. It is better to use separate hypothesis for each studied association
  • 34.
     Hypothesis (6)can be refuted because it is not stated in a measurable terms. Expression “high” is very subjective  Hypothesis (8) & (9) an be refuted because they do not reflect the study design. Although they fulfill all other criteria  Hypothesis (7) is a sound hypothesis
  • 35.
    5. RESEARCH HYPOTHESIS Subjects withHC have a higher risk of developing CAD compared to subjects without HC
  • 37.
    STUDY DESIGNS  Classification dependson role of investigator in controlling factors under study  Observational  Ecological  Cross sectional  Case control  Cohort  Experimental/interven tion  Lab experiments  Clinical trials  Community interventions  Quasi-experimental
  • 38.
    1. Ecological Study Sampling units are groups  Good source for new hypothesis  Problems Ecological fallacy Temporal relationship
  • 39.
    2. Cross SectionalStudy  Data collected at a single point in time  No control group  Prevalence rate can be calculated  Develop new hypothesis “Snapshot”
  • 40.
    Prevalence vs. Incidence Prevalence The total number of cases at a point in time  Includes both new and old cases  Incidence The number of new cases over time
  • 41.
    Example of aCross-Sectional Study Study of association between garlic consumption & CAD in the Family Practice Clinic
  • 42.
    Cross-sectional Study Sample ofPopulation Garlic Eaters Non-Garlic Eaters Prevalence of CAD Prevalence of CAD Time Frame = Present
  • 43.
  • 44.
    Cross-Sectional Study  Strengths Quick Cheap Weaknesses  Weak evidence of association  Lack of representativeness  Absence of temporal relationship  No control of confounders  Prevalence-incidence bias
  • 45.
    3. Case-Control Study Start with people who have disease  Compare them with controls that do not  Look back and assess exposures
  • 46.
    Case-Control Study Patients withCAD Patients w/o CAD Present Past High Garlic Diet High Garlic Diet Low Garlic Diet Low Garlic Diet Cases Controls
  • 47.
    Do not eat Eatgarlic ill not ill 49 49 98 4 6 10 Presentation of Case-control Study
  • 48.
    Strengths  Good forrare outcomes: cancer  Can examine many exposures  Useful to test hypothesis  Fast & easy  Cheap  Provides Odds Ratio  Minimal ethical problems  No risk to participants  No attrition problems
  • 49.
    Weaknesses  Cannot measure Incidence  Prevalence  Relative Risk  High susceptibility to bias Misclassification bias Recall bias Selection bias Confounding bias Temporal relationship
  • 50.
  • 51.
  • 52.
  • 53.
    Intuitively If the frequencyof exposure is higher among cases than controls Then the incidence rate will probably be higher among exposed than non exposed.
  • 54.
  • 55.
  • 56.
    Cohort Study  Beginwith disease-free individuals  Classify individuals as exposed/unexposed  Record outcomes in both groups  Compare outcomes using relative risk
  • 57.
  • 58.
    Calculate measure of frequency: Cumulative incidence - Incidence - Attack rate (outbreak) end of follow-up
  • 59.
  • 60.
  • 61.
    Example of aCohort Study To see the effects of smoking on lung cancer development
  • 62.
  • 63.
    Smokers Non-smokers ill not ill 706930 7000 3 2997 3000 Presentation of Cohort Data
  • 64.
    Data Analysis Incidence rate Among smokers = 70/7000=10/1000  Among non-smoker = 3/3000 = 1/1000 Relative risk = 10/1 = 10
  • 65.
    time Exposure Study starts Disease occurrence ProspectiveCohort Study Exposure Disease occurrence time Study starts
  • 66.
  • 67.
    Strengths  Provides incidencedata  Establishes time sequence for causality  Eliminates recall bias  Suitable for rare exposure  Allows for accurate measurement of exposure variables
  • 68.
    Strengths  Can measuremultiple outcomes  Can adjust for confounding variables  Can calculate relative risk Dose response can be calculated
  • 69.
    Weaknesses  Expensive  Timeconsuming  Problems of attrition  Cannot study rare outcomes (diseases)  Some ethical problems
  • 70.
    Weaknesses  Exposure maychange over time  Disease may have a long pre-clinical phase  Change of diagnostic criteria
  • 71.
    Experimental Studies Clinical trialsprovide the “gold standard” of determining the relationship between garlic and cardiovascular disease prevention.
  • 72.
    Clinical Trials  Randomized Double-blind  Placebo-controlled
  • 73.
  • 74.
  • 75.
    Strengths  Best measureof causal relationship  Best design for controlling bias  Can measure multiple outcomes
  • 76.
    Weaknesses  Ethical issues Unawareness of patients  Withholding beneficial treatment  Inability to refuse (prisoners)  Potential side effects  Co-intervention & contamination  Feasibility problems
  • 77.
    Small Group Tasks Elect a leader and a speaker  Read your scenario  Design a study to answer the research question  Your funds are not unlimited!  Briefly present your study to the large group  Time:  10 min for study design  10 min for group presentations
  • 78.
    Selection of ResearchDesign  Selection of the best research design depends on many factors  Purpose of study  State of existing knowledge  Characteristics of study variables (exposure/outcome)  Latency  Feasibility
  • 79.
    Research: The Fountainof Knowledge  A research problem refers to a difficulty that a researcher or a scientific community or an industry or a government organization or a society experiences. It may be a theoretical or a practical situation. It calls for a thorough understanding and possible solutions.  Research provides the basis for many government policies. For example, research on the needs and desires of the people and on the availability of revenues to meet the needs helps a government to prepare a budget.  It is the fountain of knowledge and provides guidelines for solving problems.