Assess HealthCare Provider Perceptions and Utilization of Patient Safety Reporting System and its Barriers in Saudi Arabian Hospitals

Assess HealthCare Provider Perceptions and Utilization of Patient Safety Reporting System and its Barriers in Saudi Arabian Hospitals: A cross sectional study

and bleow tempelt can help ypu

Requirements: ,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,

KING FAISAL SPECIALIST HOSPITAL & RESEARCH CENTER/RIYADH

TYPE YOUR TITLE HERE

PRIMARY INVESTIGATOR:

POSITION, DEPARTMENT:

CO-PRIMARY INVESTIGATOR:

POSITION, DEPARTMENT:

CO-INVESTIGATOR(S):

POSITION, DEPARTMENT:

DATE OF SUBMISSION:

REVIEWED SUBMISSION:

*Remove all the blue instructions from this template before your submission.

*Make sure that the level of English is adequate (e.g. use or ask a colleague to review as needed). Proposal with poor language quality will be returned.

*To update this Table of content, right click on the table and choose “update field”.

ABSTRACT

Background

This section briefly introduces the research topic and provides context for the study (including statistics relevant to the problem). It should explain why the research is important and relevant to the field of nursing.

Aim(s) of the study

This section highlights the purpose of conducting the study.

Method

This section outlines the methodology planned to reach the aim(s), including the study design, data collection methods, and analyses techniques.

Conclusion

This section discusses the potential implications of the study findings for the nursing practice, policies, management, or education.

Keywords (5-6):

*The abstract should not exceed 250 words.

BACKGROUND/PROBLEM

Use HEADING 1, HEADING 2, HEADING 3 from the Microsoft Word selection in the tool bar above (right side). Do not change the style (font, size, underlining). These styles are pre-programmed to allow you to update your Table of Content easily.

Use the style NORMAL for the body of the text.

REFERENCES/CITATIONS: Please use one style of reference through your proposal (e.g. APA, Harvard, Chicago).

AIM OF STUDY

List your primary aim +/- secondary aim(s). You can use bullet points if you want.

LITTERATURE REVIEW

This section will give an overview of the existing scientific literature on your topic. It should enable us to identify what is knows and the gaps. Most of the time, it should not be lengthy (2/3 to 1 page) can be adequate for most studies. If your study is more complex and more concepts needs to be explained, it can be longer.

DESIGN AND METHOD

You may write this section as a continuous paragraph, but make sure to include all the elements below, according to your study design.

Design

Describe the design of your study (e.g. cross-sectional observation study, qualitative study, retrospective chart review, interventional study).

Population

Inclusion

E.g., children from birth to 14 years of age, patient diagnosed with sickle-cell disease, able to consent independently

Exclusion

Do not write the contrary of your inclusion criteria. These are different criteria. E.g., patient is clinically unstable, patient has severe cognitive deficits, has a specific condition or is taking a specific medication.

Sample Size and Sample Selection

For a quantitative study: include the sample size calculation to achieve power analysis.

For a qualitative study: explain how you will reach data saturation.

For a retrospective chart/database/registry study: indicate the exact period covered by the review (DD-MM-YYYY to DD-MM-YYYY).

Sources of Data

List all sources from where you will get your data (e.g., sociodemographic and clinical data will be retrieved from the medical record, satisfaction scored will be gathered through Questionnaire X)

For a quantitative study:

Make a table in the Appendix and list all the variable that will be measured and their unit of measure.

If a questionnaire/tool/scale is used: describe briefly the instrument (goal, length, #item, duration to complete) and it psychometric properties (fidelity, validity), if available. If a translated version is use, it should be already validated unless you plan to validate the tool, then you need to explain how. You must also contact the original authors to get permission to use a tool unless there is a mention that it not required. Attached the license agreement or the email with the author’s permission.

For a qualitative study:

Describe how you will collect the data (e.g., semi-structured interviews).

Put the list of your questions in an Appendix. (in Arabic as well, if they will be interviewed in Arabic)

DATA COLLECTION

How and where the data will be collected?

DESCRIPTION OF THE INTERVENTION

Only for interventional studies. Remove this section, if not applicable.

DATA MANAGEMENT

Where will the data be stored confidentially? (Excel sheet with password). Who has access?

We encourage you to use the free resource REDCap to manage your data. Contact the Nursing Research team for more information about it. It makes everything simpler for most studies.

STATISTICAL CONSIDERATIONS

For a quantitative study: Planned statistical analyses, statistical significance targeted, statistical software that will be used to analyze the data (e.g., Excel, SPSS). If you need help with this section, you can contact the Nursing Research team. If your study requires complex statistical analyses, you can take an appointment on Service Hub with the Research Concierge.

For a qualitative study: explain how the data will be analyze (framework).

ETHICAL CONSIDERATIONS

Type of consent that will be uses, is a waiver for informed or signed consent is requested?

For any study involving children of 8 years and above, you need to include a Child Assent.

Explain how the confidentiality will be maintain.

If your study can cause any type of discomfort (even mild anxiety when talking about a sensitive topic), mention it here and how any distress would be addressed.

Consult the “Nursing Knowledge Base” page for more information or contact a Research Nurse Specialist.

Unless you are doing a retrospective chart/database/registry review, most study need to have either a full consent or a Participant Information sheet attached to the proposal. You can find some template on the Knowledge base page for both. Make sure the English/Arabic language is simple (8th grade level max.)

TIMEFRAME

RESEARCH TEAM’S ROLES (LEADING TO AUTHORSHIP)

E.g., study design, data collection, data analysis, statistical analyses, manuscript redaction, manuscript review

*To be consider an author on a publication, one must usually assume 3-4 roles in a research or less if a specific role is significant/

REFERENCES

Use one reference style through your proposal (e.g. APA, Vancouver, Harvard)

APPENDIX 1 VARIABLES

Remove if not applicable.

APPENDIX 2 ADD TITLE

As applicable to your study:

Add tools that will be used (questionnaires, scales)

Add permission from authors to use a tool

Add participant information sheet (can also be sent separately, if preferred)

Collepals.com Plagiarism Free Papers

Are you looking for custom essay writing service or even dissertation writing services? Just request for our write my paper service, and we'll match you with the best essay writer in your subject! With an exceptional team of professional academic experts in a wide range of subjects, we can guarantee you an unrivaled quality of custom-written papers.

Get ZERO PLAGIARISM, HUMAN WRITTEN ESSAYS

Why Hire Collepals.com writers to do your paper?

Quality- We are experienced and have access to ample research materials.

We write plagiarism Free Content

Confidential- We never share or sell your personal information to third parties.

Support-Chat with us today! We are always waiting to answer all your questions.