Chapter 3 Research Methodology
Chapter 3 Research Methodology
RESEARCH
METHODOLOGY
Chapter 3
RESEARCH METHODOLOGY
A. Research Design
B. Locale of the Study
C. Participants of the Study
D. Sampling Procedure
E. Data Gathering Instrument
F. Data Gathering Procedure
G. Analysis of Data
H. Ethical Considerations
I. QUALITATIVE
RESEARCH DESIGN
Research Design
This is a blueprint. A blueprint is a
guide for making something. It's a
design or pattern that can be
followed like what is the
measurement of height, width,
length, distance to build your
designed building, or a house.
Types of Qualitative
Research Designs
CASE STUDY
It is a research approach in a qualitative method that is used to
generate or determine an in-depth understanding of an issue in its
real-life context. It can be an investigation of a single person, group,
event or the community (Kothari 2004).
• Unstructured. Unlike the structured type of interview, unstructured type has no prepared sets of
questions for the interviewee. Here, the researcher is required to have enough knowledge of the
topic under investigation so that he/she can get the needed data without planned and guided
questions. The session is done in a natural manner of conversing and exchanging of ideas while the
reliability of obtained data is still ensured.
3. Post-data Gathering. This phase is conducted after the data have been
already collected and transcribed. Here, the researcher will present the
transcribed data to the participants in order to check the accuracy of the
collected and transcribed data. In addition, the researcher may also perform
some follow-up activities such as informal interviews to clarify some unclear
information as well as to ensure the rigor of the possible results of the study.
V. ANALYSIS OF DATA
1. Transcribing. The first step the researcher should do once he/she has obtained
data is to transcribe them. Data transcription aims to create an organized
textbased version of data gathered from interview, observation, and other types of
qualitative research tools (e.g., the researcher creates a text version of an audio
recording of the interview conducted). Moreover, data transcription enables the
researcher to immerse into the data he/she collected. This further helps him/her to
sort and organize data for easy understanding and analysis.
2. Coding. The next step the researcher should perform after transcribing the data is
to code them. Coding aims to categorize the data by creating smaller groupings
for easy analysis of the transcribed data. The formulated codes can be a word or
phrase that are used by the researcher to describe the meaning and context of the
data. These can be further created using either the prior knowledge of the
researcher as a result of reviewed literature or the observed apparent codes of the
researcher as he/she reviews the actual data. In addition, the researcher may
employ either manual or automated coding.
3. Drawing themes. The final step of data analysis deals with drawing of themes
based on the transcribed and coded data. Here, the researcher may utilize
different qualitative analyses such as the commonly used content and thematic
analysis.
V. ETHICAL
CONSIDERATIONS
1. Informed consent. Providing a consent letter informing the target participants
is necessary to be done by the researcher. The said letter or form should
primarily state the objective of the study justifying their need for participation.
Their roles, responsibilities, and rights should also be clearly discussed (e.g.,
the involvement of the participants is solely voluntary, and they have the right to
withdraw from the activity without coercion).
2. Beneficence – do not harm. The data collection procedure should not bring
any harm with the participants. The researcher should avoid decisions and
actions that may cause harms such as physical, emotional, and the like to the
participants (e.g., the researcher should be sensitive enough with the place,
time, and even the manner the data will be collected to the participants). In
addition, it is also to note that the researcher should inform the participants of
the possible risk and harm prior to the process of data collection.