exam
問題一覧
1
Pilot study
2
It reduces the random error
3
Ethics committee approval
4
'a' and 'b' are correct
5
Implementation research
6
Feasibility should not be a criterion while developing research question
7
Reliable
8
I, III, IV, II
9
True
10
To determine the association of maternal smoking during pregnancy with respiratory infectious disease morbidity and mortality in infants
11
Critical appraisal
12
It is not necessary to address the weakness of the study in a scholarly manner
13
It helps the researcher in arriving the conclusion of a study
14
False
15
MeSH is used for EMBASE database
16
4.71
17
Case fatality ratio
18
Low prevalence and high incidence
19
Disease specific mortality
20
Numerator has number of new cases
21
Cross-sectional study
22
There is no comparison group
23
Cohort study
24
Risk factors of the disease
25
Compare the study outcomes for 2 group
26
Risk ratio
27
Less than 1
28
Incidence in exposed is higher than unexposed
29
Both (ii) and (iv)
30
False
31
All clinical trials must be blinded
32
Loss to follow up of study participants does not affect the study outcome
33
To get groups with comparable baseline characteristics
34
Avoid observer and participant bias
35
Placebo
36
Adequate sample size
37
Prevarication
38
At any of the above stages
39
Information bias
40
False
41
Focus Group Discussions and In-depth interviews
42
Content analysis
43
Observer becomes a part of the event/group
44
Heterogeneity of the group is a pre-requisite
45
Structured questionnaire-based interviews
46
26
47
10%
48
It covers the middle 50% of observations
49
Continuous
50
12.0
51
The magnitude of error can be measured in probability samples
52
Quota sampling is a type of non-probability sampling
53
True
54
Convenience sampling
55
Sampling frame
56
80%
57
Allocated budget
58
138
59
Can be defined as the probability of correctly rejecting null hypothesis when it is false
60
a' and 'b'
61
The degree to which the inferences drawn from a study can be generalized to a broader population beyond the study population
62
Target population
63
Feasibility
64
Internal validity
65
Adequate sample size
66
Only 'a'
67
Serious interpretation difficulties in analysis and interpretation
68
Experiences shared by victims of domestic violence
69
Prospective cohort study
70
a' and 'c
71
Open-ended questions
72
Judgments
73
Review of records
74
Stimulate memory
75
From intimate to casual
76
Manipulation of data
77
Field supervisor
78
Repetition of data collection in a randomly selected subset in the same population
79
Onsite training is not essential for data collectors
80
True
81
Record
82
True
83
c) Normalized database does not facilitate further data aggregation
84
Applying for the ethics committee clearance
85
Media, location and backup information
86
Univariate analysis, stratified analysis and multivariate analysis
87
D, B, C, F, E, G, A
88
Cohort study - relative risk
89
We compare the study outcome for 2 groups
90
False
91
Undue inducement
92
IC taken by coercion is considered valid
93
Autonomy
94
Consent from the tribal head (Group consent) is desirable
95
Non-Maleficence
96
Nuremberg code
97
Analysis of mortality data of 2001-2010
98
Archival for a period of 5 - 15 years as per the requirement of the sponsor may be necessary
99
Close watch on enrolment targets
100
Regulatory review
問題一覧
1
Pilot study
2
It reduces the random error
3
Ethics committee approval
4
'a' and 'b' are correct
5
Implementation research
6
Feasibility should not be a criterion while developing research question
7
Reliable
8
I, III, IV, II
9
True
10
To determine the association of maternal smoking during pregnancy with respiratory infectious disease morbidity and mortality in infants
11
Critical appraisal
12
It is not necessary to address the weakness of the study in a scholarly manner
13
It helps the researcher in arriving the conclusion of a study
14
False
15
MeSH is used for EMBASE database
16
4.71
17
Case fatality ratio
18
Low prevalence and high incidence
19
Disease specific mortality
20
Numerator has number of new cases
21
Cross-sectional study
22
There is no comparison group
23
Cohort study
24
Risk factors of the disease
25
Compare the study outcomes for 2 group
26
Risk ratio
27
Less than 1
28
Incidence in exposed is higher than unexposed
29
Both (ii) and (iv)
30
False
31
All clinical trials must be blinded
32
Loss to follow up of study participants does not affect the study outcome
33
To get groups with comparable baseline characteristics
34
Avoid observer and participant bias
35
Placebo
36
Adequate sample size
37
Prevarication
38
At any of the above stages
39
Information bias
40
False
41
Focus Group Discussions and In-depth interviews
42
Content analysis
43
Observer becomes a part of the event/group
44
Heterogeneity of the group is a pre-requisite
45
Structured questionnaire-based interviews
46
26
47
10%
48
It covers the middle 50% of observations
49
Continuous
50
12.0
51
The magnitude of error can be measured in probability samples
52
Quota sampling is a type of non-probability sampling
53
True
54
Convenience sampling
55
Sampling frame
56
80%
57
Allocated budget
58
138
59
Can be defined as the probability of correctly rejecting null hypothesis when it is false
60
a' and 'b'
61
The degree to which the inferences drawn from a study can be generalized to a broader population beyond the study population
62
Target population
63
Feasibility
64
Internal validity
65
Adequate sample size
66
Only 'a'
67
Serious interpretation difficulties in analysis and interpretation
68
Experiences shared by victims of domestic violence
69
Prospective cohort study
70
a' and 'c
71
Open-ended questions
72
Judgments
73
Review of records
74
Stimulate memory
75
From intimate to casual
76
Manipulation of data
77
Field supervisor
78
Repetition of data collection in a randomly selected subset in the same population
79
Onsite training is not essential for data collectors
80
True
81
Record
82
True
83
c) Normalized database does not facilitate further data aggregation
84
Applying for the ethics committee clearance
85
Media, location and backup information
86
Univariate analysis, stratified analysis and multivariate analysis
87
D, B, C, F, E, G, A
88
Cohort study - relative risk
89
We compare the study outcome for 2 groups
90
False
91
Undue inducement
92
IC taken by coercion is considered valid
93
Autonomy
94
Consent from the tribal head (Group consent) is desirable
95
Non-Maleficence
96
Nuremberg code
97
Analysis of mortality data of 2001-2010
98
Archival for a period of 5 - 15 years as per the requirement of the sponsor may be necessary
99
Close watch on enrolment targets
100
Regulatory review