Q3 Week 1 Research Design 1
Q3 Week 1 Research Design 1
C. CROSS-SECTIONAL STUDIES
- THOSE IN WHICH DATA COLLECTION IS STRICTLY IN THE PRESENT
TIME.
3. THE SUBJECTS TO BE INCLUDED IN THE RESEARCH.
Symbol Meaning
X Treatment
O Observation
R Randomization
EG Experimental Group
CG Control Group
TE Treatment effect
TYPES OF EXPERIMENTAL DESIGN
A. PRE-EXPERIMENTAL DESIGN
Design 1. One-Shot Case Study- considers
only one group exposed to an experimental
variable/treatment (X) and then given a post-
test (O). It is devoid of controls.
Design 2. The One-Group Pre-test-Post-test Design-
this is the improvement of the first design, with the giving of
a pretest (O1) prior to the introduction of the experimental
variable/treatment (X) and post tested (O2).
Design 3. The Static-Group Comparison Design- This is
a design in which a group which has experienced
experimental variable/treatment (X) is compared with one
which has not for the purpose of establishing the effect of X.
This design involves two (2) groups, the experimental group
and the control group, and both are post-tested.
A.The True Experimental Design. It controls for
nearly all sources of internal and external validity. It is
the most scientific experimental design.
Design 1. The Pretest-Posttest Control Group Design- It
involves two groups, both of which are formed by random
assignment. Both groups are pre-tested and post-tested but
only one group is given the experimental variable/treatment
(X). Threats to internal validity are prevented by means of a
second group. Maturation and testing for instance, are
manifested equally to both groups and so is regression.
Selection in taken care of by randomization.
Design 2. The Post-test Only Control Group Design. It
involves two groups, one of them receives the experimental
variable/treatment (X); both are post tested but are not pre-
tested. It is commonly confused with static group comparison
design but its difference with the latter lies on randomization.
This design is considered the last two groups of the Solomon
Four- Group design. The combination of random assignment
and the presence of control group control the sources of
internal validity except on mortality..
Design 3. The Solomon Four-Group Design – It
involves random assignment of subjects to four groups; two
(2) groups are pretested and the other two are not; one of
the pre-tested groups and one of the unpre-tested groups
receives the experimental variable/treatment (X).
C. Quasi-Experimental Design. It is quicker to use
and less expensive. It aims to establish a cause and
effect relationship between an independent and
dependent variable. But do not involve randomization.
Design 1. Time Series Design- It is an
elaboration of the one-group pretest- posttest
design in which one group is,
-repeatedly pre-tested,
-exposed to a treatment, and
-repeatedly post tested.
DESIGN 2. NON-EQUIVALENT CONTROL GROUP
DESIGN – IT IS LIKE THE PRE-TEST POSTTEST CONTROL
GROUP DESIGN. BUT IT DOES NOT INVOLVE RANDOM
ASSIGNMENT. THE BROKEN LINE BETWEEN THE TWO (2)
GROUPS SUGGESTS NO RANDOMIZATION DONE. THE LACK
OF RANDOM ASSIGNMENT ADDS A SOURCE OF INVALIDITY
NOT ASSOCIATED WITH THE PRE-TEST POSTTEST CONTROL
NOTE:
NONEQUIVALENT DESIGN IS RECOGNIZED AS WELL
WORTH USING IN MANY INSTANCES IN WHICH DESIGN
#1, #2 AND #3 OF THE TRUE EXPERIMENTAL DESIGNS
ARE IMPOSSIBLE TO USE.
DESIGN 3. COUNTER-BALANCE DESIGN – ALL
GROUPS RECEIVE ALL TREATMENTS BUT IN A
DIFFERENT ORDER. THE ONLY RESTRICTION IS THAT
THE NUMBER OF CONTROLLED GROUPS. IT WAS
ALSO NAMED “ROTATION EXPERIMENT” (MCCALL,
1923); “COUNTERBALANCED DESIGN”
(UNDERWOOD 1949); “CROSS-OVER DESIGN”
(COCHRAN AND COX 1957); “SWITCH-OVER
DESIGN” (KEMPTHORNE 1952); AND “LATIN-SQUARE
ARRANGEMENT” (CAMPBELL AND STANLEY 1963).
Time 1 Time 2 Time 3 Time 4
Group A X 1O X 2O X 3O X 4O
Group B X 2O X 4O X 1O X 3O
Group C X 3O X 1O X 4O X 2O
Group D X 4O X 3O X 2O X 1O
III. STATISTICAL DESIGN
IT IS A METHOD FOR PLANNING AND CONDUCTING EXPERIMENTS WHEN
INVESTIGATING RELATIONS BETWEEN INPUT AND OUTPUT TO A PROCESS.
A. COMPLETE RANDOMIZED DESIGN (CRD)
• IT IS A DESIGN WHERE THE TREATMENTS ARE ASSIGNED
COMPLETELY AT RANDOM SO THAT EACH EXPERIMENTAL UNIT
HAS THE SAME CHANCE OF RECEIVING ANY ONE TREATMENT.
NOTE:
FOR CRD, ANY DIFFERENCE AMONG EXPERIMENTAL UNITS
RECEIVING THE SAME TREATMENT IS CONSIDERED AS EXPERIMENTAL
ERROR. HENCE, CRD IS APPROPRIATE ONLY FOR EXPERIMENTS
WITH HOMOGENEOUS EXPERIMENTAL
UNITS, SUCH AS LABORATORY EXPERIMENTS
WHERE ENVIRONMENTAL EFFECTS ARE
RELATIVELY EASY TO CONTROL. FOR FIELD
EXPERIMENTS, WHERE THERE IS GENERALLY
LARGE VARIATION AMONG EXPERIMENTAL
PLOTS IN SUCH ENVIRONMENTAL FACTORS AS
SOIL, THE CRD IS RARELY USED.
STEP-BY-STEP PROCEDURE FOR RANDOMIZATION AND LAYOUT OF CRD:
1. DETERMINE THE TOTAL NUMBER OF EXPERIMENTAL UNITS (N): AS THE PRODUCT
OF THE NUMBER OF TREATMENTS (T) AND THE NUMBER OF REPLICATIONS (R);
THAT IS,
EXAMPLE:
N=RT
N=5 X 4 = 20. HERE, ONE POT WITH A SINGLE PLANT IN IT MAY BE
CALLED A UNIT/PLOT. IN CASE THE NUMBER OF REPLICATIONS IS NOT THE
SAME FOR ALL THE TREATMENTS, THE TOTAL NUMBER OF EXPERIMENTAL
UNITS IS OBTAINED AS THE SUM OF THE REPLICATIONS FOR EACH
TREATMENT.
2. ASSIGN A NUMBER TO EACH EXPERIMENTAL
UNIT/PLOT IN ANY CONVENIENT MANNER;
CONSECUTIVELY FROM 1 TO N.
3. ASSIGN THE TREATMENTS TO THE EXPERIMENTAL
UNITS/PLOTS RANDOMLY USING A TABLE OF
RANDOM NUMBERS OR DRAW LOTS TO OBTAIN THE
EXPERIMENTAL UNITS.
EXAMPLE: N=20
RANDOM NUMBER: 37, 80, 76, 02, 65, 27, 54, 77, 48, 73
SEQUENCE: 1, 2, 3, 4, 5, 6, 7, 8, 9,10
RANDOM NUMBERS: 86, 30, 67, 05, 50, 31, 04, 18, 41,
89
SEQUENCE: 11, 12, 13, 14, 15, 16, 17, 18, 19, 20
4. RANK THE N RANDOM NUMBERS OBTAINED IN
ASCENDING
RANDOM
NO.
OR DESCENDING
SEQUENCE RANK
ORDER.
RANDOM
NO.
SEQUENCE RANK
37 1 8 86 11 19
80 2 18 30 12 6
76 3 16 67 13 14
02 4 1 05 14 3
65 5 13 50 15 11
27 6 5 31 16 7
54 7 12 04 17 2
77 8 17 18 18 4
48 9 10 41 19 9
73 10 15 89 20 20
5. DIVIDE THE N RANKS DERIVED INTO T GROUPS,
EACH CONSISTING OF R NUMBERS, ACCORDING
TO THE SEQUENCE IN WHICH THE RANDOM
NUMBERS APPEARED.
EXAMPLE: THE 20 RANKS ARE DIVIDED INTO 4
GROUPS,
NO. EACH CONSISTING OF 5 NUMBERS.
GROUP RANKS IN THE GROUP
1 8 13 10 14 2
2 18 5 15 3 4
3 16 12 19 11 9
4 1 17 6 7 20
6. ASSIGN THE TREATMENTS (T) TO THE EXPERIMENTAL
UNITS/PLOTS (N), BY USING THE GROUP NUMBER AS
THE TREATMENT NUMBER AND THE CORRESPONDING
RANKS IN EACH GROUP AS THE PLOT NUMBER IN WHICH
THE CORRESPONDING TREATMENT IS TO BE ASSIGNED.
EXAMPLE:
• THE FIRST GROUP IS ASSIGNED TO TREATMENT A
(PLOTS 8, 13, 10, 14, 2);
• THE SECOND GROUP IS ASSIGNED TO TREATMENT
B (PLOTS 18, 5 , 15, 3, 4);
• THE THIRD GROUP IS ASSIGNED TO TREATMENT C (PLOTS 16, 12,
19, 11, 9)
• THE FOURTH GROUP IS ASSIGNED TO TREATMENT D (PLOTS 1, 17,
1 2 3 4
6, 7, 20) PLOT
TREATME D A B B
NT
5 6 7 8
B D D A
9 10 11 12
C A C C
13 14 15 16
A A B C
17 18 19 20
D B C D
THE MAJOR ADVANTAGE OF CRD IS THE SIMPLICITY IN THE
COMPUTATION OF ITS ANALYSIS OF VARIANCE ESPECIALLY
WHEN THE NUMBER OF REPLICATIONS IS NOT UNIFORM FOR
ALL TREATMENTS.
B. RANDOMIZED COMPLETE BLOCK DESIGN (RCBD)
• IT DIVIDES THE EXPERIMENTAL SUBJECTS INTO MORE
OR LESS HOMOGENEOUS GROUPS CALLED BLOCKS THEN
THE TREATMENT/INTERVENTION GETS RANDOMLY ASSIGNED
WITHIN EACH BLOCK.
• BLOCKING IS DONE TO MAKE SURE THAT THE
EXPERIMENTAL SUBJECTS IN A GROUP HAVE SIMILAR
CHARACTERISTICS SO
THAT THE OBSERVED DIFFERENCES AMONG THE
GROUPS WILL BE LARGELY DUE TO THE
TREATMENTS.
• BLOCKING ALSO HELPS IN GIVING MORE
ACCURATE RESULTS THAN THE CRD.
• THERE ARE NO RESTRICTIONS AS TO THE
NUMBER OF TREATMENTS OR NUMBER OF
BLOCKS IN THE EXPERIMENTS.
HOWEVER, IT IS DIFFICULT TO FORM BLOCKS WITH
HOMOGENEOUS EXPERIMENTAL UNITS AND A LARGE
ERROR WILL BE OBTAINED WHEN VARIATIONS AMONG
EXPERIMENTAL SUBJECTS WITHIN A BLOCK IS LARGE.
NOTE:
RCBD IS MOST APPROPRIATE TO USE IF:
1. THE SUBJECTS CAN BE CATEGORIZED ACCORDING
TO CERTAIN CHARACTERISTICS LIKE GENDER, AGE,
WEIGHT, AND HEIGHT WHICH CAN AFFECT
COMPARISON OF TREATMENTS; AND
2. A FEW DROP-OUTS ARE EXPECTED.
EXAMPLE:
HOW WILL YOU DESIGN AN EXPERIMENT WITH FOUR
(4) TREATMENTS REPLICATED THREE (3) TIMES?
SOLUTION:
RANDOMIZATION WILL BE DONE BLOCK BY BLOCK USING A
TABLE OF RANDOM NUMBERS. IN THIS EXPERIMENT,
THERE WILL BE THREE (3) BLOCKS SINCE THERE ARE 3
REPLICATES. IN EACH BLOCK THE FOUR (4) TREATMENTS
ARE ASSIGNED
RANDOMLY TO EACH OF THE 4 SUBJECTS. FOR
THE FIRST BLOCK WE GET THE FOLLOWING:
C. PHENOMENOLOGICAL METHOD
• IT IS A QUALITATIVE RESEARCH APPROACH THAT SEEKS TO
UNDERSTAND AND DESCRIBE THE UNIVERSAL ESSENCE OF
A PHENOMENON.
• THE APPROACH INVESTIGATES THE EVERYDAY
EXPERIENCES OF HUMAN BEINGS WHILE SUSPENDING
THE RESEARCHERS’ PRECONCEIVED ASSUMPTIONS
•ABOUT
In other words, phenomenological
THE PHENOMENON.