SALUM (Research Proposal)
SALUM (Research Proposal)
SALUM (Research Proposal)
YEAR, 2023
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Table of Contents
Acknowledgement.....................................................................................................................iii
Acronyms and abbreviations.....................................................................................................iv
Abstract.......................................................................................................................................v
CHAPTER ONE.........................................................................................................................1
1.0 Introduction..........................................................................................................................1
1.1 Background...........................................................................................................................1
1.2 Statement of the problem......................................................................................................2
1.3 Rationale of the study...........................................................................................................4
1.4 Research objectives..............................................................................................................4
1.5 Research Questions...............................................................................................................4
1.6 Research variables................................................................................................................4
1.7 Hypothesis formulation:.......................................................................................................5
CHAPTER TWO........................................................................................................................6
2.0 Literature review...................................................................................................................6
CHAPTER THREE....................................................................................................................8
3.0 Research methodology.........................................................................................................8
3.1 Study design.........................................................................................................................8
3.2 Study area.............................................................................................................................8
3.3 Study population...................................................................................................................8
3.4 Sampling procedure..............................................................................................................8
3.5 Sample size...........................................................................................................................8
3.6 Plan for data collection and technique..................................................................................8
3.7 Data management and analysis.............................................................................................9
3.8 Dissemination of results.......................................................................................................9
3.9 Ethical consideration............................................................................................................9
3.8 Pre-test..................................................................................................................................9
3.9 Limitations of the study........................................................................................................9
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APPENDICES..........................................................................................................................10
Appendix 1; Work plan schedule.............................................................................................10
Appendix 2; study design budgeting........................................................................................10
Appendix 3; Quantitative Data Collection Tool (Structured Questionnaire)...........................11
References................................................................................................................................16
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Acknowledgement
It not easy to complete research proposal without the help of God and supportive contribution from
others. Special thanks to the ministry of health for introducing research as project in training
process for Clinical Medicine as this will help to widen our knowledge, thanks to all staff of Geita
Hospital for their support during my study and special thanks to Mr. Kiswebe who taught and
directed me on how to write the research proposal as well as Madam Grory who is my supervisor
during the research study.
Lastly, I would like to thank my fellow students who helped me in one way or another in writing
my research proposal.
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ACRONYMS AND ABBREVIATIONS
AIDS- Acquired Immune Deficiency Syndrome
ART- Anti-Retroviral Therapy
ARV - Anti- retroviral
CD4+ - Cluster of Differentiation
HAART-Highly Active Anti-retroviral Therapy
HIV- Human Immuno-Deficiency Virus
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CHAPTER ONE
1.0 Introduction
Antiretroviral therapy (ART) is the recommended treatment for HIV. ART involves taking
a combination of anti-HIV medications (a regimen) every day. Anti-HIV medications which
are also called antiretroviral are grouped into six drug classes according to how they fight
HIV. The six classes are non-nucleoside reverse transcriptase inhibitors (NNRTIs),
nucleoside reverse transcriptase inhibitors (NRTIs), protease inhibitors (PIs). These are also
commonly referred to as HAART a regimen that is Highly Active AntiretroviralTherapy.
ART are used to keep HIV infections under control. This because, these drugs tend to
suppress the growth and development of the Human Immunodeficiency Virus in the HIV
infected patient and help in reducing disease progression hence reduces the HIV related
mortality.
There drugs reduce the viral load that is the amount of virus in the bloodstream. In some
people viral load can become so low that it is undetectable by the viral load test but this does
not mean that the all virus is gone and does not mean that the person is cured of HIV
infection. However, these people are less likely to transmit HIV infection to others.
ART also prevents onward transmission of HIV to sexual partner and mother to child
transmission. Huge reductions have been seen in rates of death and infections when the use is
made of a potent ARV regimen, particularly in early stages of the disease.
1.1 Background
According to the world organization, antiretroviral therapy (ART) is combination of
several drugs which was introduced in the management of patients living with HIV or
AIDS. As of December 2017, an estimated 21.7 million people globally were receiving
antiretroviral therapy. This represented an increase of 2.3 million people over the number
receiving such treatment 12 months earlier. Of all persons living with HIV 59% [44−73%]
had obtained antiretroviral therapy in 2017.
In the WHO African Region, 60% [45−73%] of people living with HIV were able to
access life-saving medicines in 2017. Similarly, 66% [48−84%] in the Region of the
Americas, 18% [12−26%] in the Eastern Mediterranean Region, 54% [43−62%] in the
European Region, 51% [34−70%] in the South-East Asia Region and 62% [45−82%] in
the Western Pacific Region were accessing such treatment. It is increasingly clear that
everyone infected with HIV will eventually need treatment. With an estimated 36.9
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million [31.1–43.9 million] million people now living with HIV globally, this represents a
significant need to scale up HIV testing and treatment, while continuing to invest in
prevention and other programmes to combat new infections.
Overall antiretroviral therapy coverage among children was lower than among adults.
Children represented 4% of the people receiving antiretroviral therapy and also
approximately 5% of the people living with HIV. Of the 1.8 million [1.3–2.4 million]
children estimated live with HIV, 52% [33–70%] had access to treatment versus 59% [44–
73%] of adults.
Access to ART has increased rapidly since 2005 from just 2.1 million to 21.7 million by
the end of 2017. The estimated ART global coverage increased from 7% in 2005 to 59%
in 2017. The greatest increase occurred in WHO African Region, where ART was
uncommon up to 2005 (758 000 people on ART) and increased to 15.4 million in 2017.
Regions that have made less progress are those in which the epidemic is predominantly
concentrated in populations with lower access and utilization of services, such as sex
workers, injecting drug users, and men who have sex with men.
According to WHO, the HIV or AIDS patient who adhere well to the prescribed ART can
achieve viral suppression as a benefit of ART such as immune restoration, prolonged
survival, reduce resistance, improve quality of life and treatment as prevention.
However, despite of the education provided to the HIV or AIDS patient as well as the care
giver on the benefits of ART compliance, there are some patients who still fail to take ARV
drugs as directed by the health care provider by leaving behind the course of treatment and
others tend to refuse to initiate the HIV treatment regimen after being diagnosed as HIV
infected.
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1.3 Rationale of the study
This study aims to identify possible factors related to poor adherence of ART among
people living with HIV (PLHIV) and to find their solutions as well as to expand
knowledge about effective compliance of ART regimen as this can make people aware
of the importance of effective use of ART.
Specific objectives
To assess the knowledge of ART adherence among the patient living with HIV or
AIDS at GEITA CTC CLINIC
To determine acceptance on ART among patient living with HIV or AIDS.
To establish perceptions towards adherence to ART among AIDS patients.
Identify accessibility of ART to the patients living with HIV or AIDS at GEITA CTC
CLINIC
1.5 Research Questions
How does poverty influence to poor-adherence of ART among HIV/AIDS patients?
Does patients’ perception towards ART hinders adherence to the ARV regimen
among HIV/AIDS patients?
How do accessibility of ARV influence adherence to ART regimen among HIV/AIDS
patients?
1.6 Research variables
The variables of this study are:
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CHAPTER TWO
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from work to get prescriptions, mainly because they do not want to disclose their HIV status
to employers out of fear of discrimination. With soaring unemployment rates (24% as of
2014) and widespread food insecurity, few patients are willing to risk their jobs, especially
when only one in five households in the country currently meets its dietary energy needs.
Poverty
There is a relationship between food and medication that extends even further beyond the
income argument. Some classes of antiretroviral drugs (such as Saquinvair and Nelfinavir)
actually cause adverse side effects when taken without food, such as nausea, vomiting, and
stomach pain. On the other hand, other classes of drugs (such as Didanosine and Indinavir)
cause side effects when taken with food, such as increased appetite. For patients living in
poverty, reducing these negative side effects naturally become priorities in the context of
scarce food and income. In this case, non-adherence seems more convenient and
advantageous to the patient.
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CHAPTER THREE
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charts, bar and line graphs and frequency tables. Descriptive statistics such as mean,
frequencies and percentages will be used to describe and summarize the data.
3.8Dissemination of results
At the end, the results will be disseminated to Care and Treatment Clinic (CTC) at Geita
Hospital, to Geita School of Nursing and Midwifery for the purpose of keeping references for
the College, and other remained to researcher.
3.9Ethical consideration
Letter for requesting permission to conduct research will be sent to managing medical
directors Geita Hospital for asking permission. Also permission will be requested from
respondents before interviewing them therewas no any names of respondents mentioned on
the questioner and hence confidential will be maintained.
3.8 Pre-test
This will be done to three HIV infected patients at medical ward at Geita Hospital.
Language barrier; this hindered during data collection because some of the respondents use
local language hence facing difficulties when communicating with them during interviewing
or answering of questions, so for this case the researcher will be supposed to have a person
who can translate.
Time; time will be limited for data collection the analysing and interpreting of research
findings
Financial; lack of enough money will be a problem due to expensiveness during printing and
typing.
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References
Lipincott, W., & Wilkins.(2007). Patients Perception of HAART in relation to treatment
uptake and adherence. Epidemiology and Social Sciencies
Nakiyemba A., Aurugai D.A., Kwasa R., Oyobba T (2005). Factors that facilitate or constrain
adherence to antiretroviral therapy among adults in Uganda: A- Pre-Intervention Study
Briggs, C.L. (1992). Learning How to Ask. A Sociolinguistic Appraisal of the Interview in
Walonick, D.S. (2005). Elements of a Research Proposal and Report. Retrieved from
http://www.statpac.com/research-papers/research-proposal.htm (date unknown).
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SALUM JABILI
SCHOOL OF NURSING AND MIDWIFERY
GEITA
P.O BOX 136
GEITA TC- GEITA
THE MANAGING MEDICAL DIRECTOR
GEITA REFERAL HOSPITAL
P. O. BOX
GEITA
UFS
THE PRINCIPAL
GEITA SCHOOL OF NURSING AND MIDWIFERY
P. O. BOX 40
GEITA
Dear Sir
Your faithfully:
……………………………………
SalumJabili
Copy to:-
CTC In charge
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a. Research work plan and budget
b. 3.9.1 Research work plan
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Prepare proposal A-4 papers Ream 1 @10000/= 10,000/=
Total 10400/=
Total 5000/=
Total 2,600/=
Total 30,000/=
Total 73900/=
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