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A Quasi Experimental Study to Evaluate the Effectiveness of Information Education and Communication Package on Knowledge Regarding Impact of Mobile Phone Usage During Pregnancy Among Antenatal Women in s
A Quasi Experimental Study to Evaluate the Effectiveness of Information Education and Communication Package on Knowledge Regarding Impact of Mobile Phone Usage During Pregnancy Among Antenatal Women in s
package on knowledge regarding impact of mobile phone usage during pregnancy among antenatal
women in selected health centers in thajavur district.
OBJECTIVES 1. To assess the existing level of knowledge and practice regarding self-care among
diabetes mellitus patients on Insulin therapy in experimental group and control group. 2. To assess the
effectiveness of information education and communication package on knowledge and practice regarding
self-care among diabetes mellitus patients on Insulin therapy in experimental group. 3. To correlate the
posttest level of knowledge and practice regarding self-care among diabetes mellitus patients on Insulin
therapy in experimental group and control group. 4. To determine the association between selected de
OBJECTIVES
1. To assess the existing level of knowledge regarding impact of mobile phone usage during pregnancy
among antenatal women in experimental group and control group.
communication package on knowledge regarding impact of mobile phone usage during pregnancy
among antenatal mothers in experimental group.
3. To correlate the posttest level of knowledge regarding impact of mobile phone usage during pregnancy
among antenatal women in experimental group and control group.
4. To determine the association between selected demographic variables and pretest level of knowledge
and also selected demographic variables and posttest level of knowledge regarding impact of mobile
phone usage during pregnancy among antenatal mothers in experimental group and control group.
theory
E O1 X O2
C O1 O2
check list
DATA COLLECTION
DATA ANALYSIS
control group.
experimental group.
RESEARCH METHODOLOGY
analyzing data.
procedure, reliability, pilot study, data collection procedure and plan for data
analysis.
RESEARCH APPROACH
RESEARCH DESIGN
EXPERIMENTAL GROUP O1 X O2
CONTROL GROUP O3 O4
O1 - Pre-test
X - Treatment
O2 - post test
O3 - Pre-test
O4 - Post test
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clock. The number of diabetic out-patients will be 15-20 and in-patients will
be 10-15. The setting was selected on the basis of feasibility and also the
department. Also the hospital has advanced diagnostic laboratory. It also has
diabetic out-patients and in-patients department. The number of diabetic outpatients will be 15-20 and in-
patients will be 10-15.The reason for selecting
this hospital was the availability of samples, facility for the study and
expectation of cooperation from the medical and nursing staff for collection
of data.
POPULATION
The target population of this study was diabetes mellitus patients (In
SAMPLE
(in patients & out patients) on insulin therapy at G.V.N Hospital and
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SAMPLE SIZE
Hospital)
SAMPLING TECHNIQUE
study.
INCLUSION CRITERIA
EXCLUSION CRITERIA
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checklist on self-care.
SCORING PROCEDURE
SECTION II
The total score was 25.Ascore of 1 mark was given for every correct
answer and zero was given for every wrong answer. A score was ranged as
follows
Level of knowledge
SECTION III
The total score was 20.Ascore of 1 mark was given for every correct
answer and zero was given for every wrong answer. A score was ranged as
follows
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Level of practice
VALIDITY
The tool was evaluated by 5 experts who were requested to give their
RELIABILITY
mellitus patients on insulin therapy, who were not included in main study.
Reliability of the tool was assessed by split half method and inters rater
PILOT SYUDY
for experimental group. After obtaining oral consent from the diabetes
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group. For control group pretest was given and after 1week posttest was
given. The pilot study was designed to find out the feasibility of the tool and
group design was used. The data were collected for 6 day a week. The timing
of data collection was from 9.00am to 5.00 pm. The researcher identified the
samples. Five to ten samples were selected per day depending on the
availability. The researcher first meets the samples, rapport was developed
and the researcher obtained written consent from all samples. The nature and
purpose of the study was explained to the selected samples. First pre
will be collected from them for scoring. The information education and
minutes and demonstration on insulin administration and foot care was also
given. The adequate time was given to all study samples to clarify the
based on the questionnaire. In control groups the pretest and posttest was
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demographic data.
Paired„t‟ test was used to compare the pretest and the post test scores
variables with pretest and posttest level of knowledge and practice scores.
ETHICAL CONSIDERATION
Formal permission from the principal and head of the department was
obtained prior to the study. Also formal written letter was given to director
consent was obtained before administration of tool. The samples are assured
withdraw from the study at any time. The purpose of the study was explained