Anthony Yacoub
Professor Gideonese
PH 195W
27 April 2021
National Institute of Dental and Craniofacial Research
The name of my sub-agency is the National Institute of Dental and Craniofacial Research
(NIDCR) and the name of my selected study section is The Oral, Dental and Craniofacial
Sciences. I chose this sub-agency because it closely ties to my practicum site and lead article
because of the mentioning of dentistry and the projects that I work on with internship. The
projects I work on with my internship deals with oral hygiene which is what this study section
and sub-agency work with. The sub-agency provides leadership for national research to be
designed to help understand, treat, and prevent infectious and inherited craniofacial-oral-dental
diseases that take away many people’s lives. The Oral, Dental and Craniofacial Sciences study
section works a lot with the investigation of teeth and the oral cavity. They deal with the
development of oral hard tissue and enamel. Periodontal bone remodeling and pathogenesis of
oral and dental diseases are also featured. The National Institute of Dental and Craniofacial
Research holds its funding priorities in oral health and overall health. They visioned a plan from
2020-2025 to focus on a future of dental, oral, and craniofacial health and diseases as they are
understood in the context of the whole body. In this case, the specified area of focus for both the
sub-agency and the study section overlap. The study section mentioned also works on various
studies that also relate to the overall health of individuals rather than just focusing strictly on the
oral cavity and the health of the teeth. The National Institute of Dental and Craniofacial Research
offer grant programs that include: Oral and Comprehensive Health, Oral and Salivary Cancer
Biology, Oral Health Disparities and Inequities, and many others that are oral concentrated as
well as grants that deal with the overall health of an individual. This agency includes a list of
funding opportunities that could easily be found and include application forms for easy access on
the same page. The goal of this agency is clear and the intentions are straightforward as it sets an
aim to advance the nation’s oral health through research and innovation.
State Application Identifier
Applicant Identifier
1. TYPE OF SUBMISSION 4. a. Federal Identifier
5. APPLICANT INFORMATION Organizational DUNS:
Legal Name:
Department: Division:
Street1:
Street2:
City:
State:
Country: ZIP / Postal Code:
Person to be contacted on matters involving this application
First Name: Middle Name:
Last Name: Suffix:
Phone Number: Fax Number:
Email:
6. EMPLOYER IDENTIFICATION (EIN) or (TIN):
7. TYPE OF APPLICANT:
Other (Specify):
Small Business Organization Type Women Owned Socially and Economically Disadvantaged
If Revision, mark appropriate box(es).
9. NAME OF FEDERAL AGENCY:
A. Increase Award B. Decrease Award C. Increase Duration D. Decrease Duration
E. Other (specify):
10. CATALOG OF FEDERAL DOMESTIC ASSISTANCE NUMBER:
Is this application being submitted to other agencies?
TITLE:
11. DESCRIPTIVE TITLE OF APPLICANT’S PROJECT:
2. DATE SUBMITTED
3. DATE RECEIVED BY STATE APPLICATION FOR FEDERAL ASSISTANCE
SF 424 (R&R)
County / Parish:
Province:
Prefix:
What other Agencies?
Pre-application Application Changed/Corrected Application
New Resubmission
Renewal Continuation Revision
Yes No
8. TYPE OF APPLICATION:
OMB Number: 4040-0001
Expiration Date: 12/31/2022
b. Agency Routing Identifier
12. PROPOSED PROJECT:
Start Date Ending Date
13. CONGRESSIONAL DISTRICT OF APPLICANT
c. Previous Grants.gov
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SF 424 (R&R) APPLICATION FOR FEDERAL ASSISTANCE Page 2
15. ESTIMATED PROJECT FUNDING
a. Total Federal Funds Requested
17. By signing this application, I certify (1) to the statements contained in the list of certifications* and (2) that the statements herein are
true, complete and accurate to the best of my knowledge. I also provide the required assurances * and agree to comply with any resulting
terms if I accept an award. I am aware that any false, fictitious. or fraudulent statements or claims may subject me to criminal, civil, or
administrative penalties. (U.S. Code, Title 18, Section 1001)
19. Authorized Representative
First Name: Middle Name:
Last Name: Suffix:
Position/Title:
Organization:
Department: Division:
Street1:
Street2:
City:
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Phone Number: Fax Number:
Email:
Signature of Authorized Representative Date Signed
20. Pre-application
*The list of certifications and assurances, or an Internet site where you may obtain this list, is contained in the announcement or agency specific instructions.
County / Parish:
c. Total Federal & Non-Federal Funds
18. SFLLL (Disclosure of Lobbying Activities) or other Explanatory Documentation
Province:
b. Total Non-Federal Funds
Prefix:
First Name: Middle Name:
Last Name: Suffix:
Position/Title:
Organization Name:
Department: Division:
Street1:
Street2:
City:
Country: ZIP / Postal Code:
Phone Number: Fax Number:
Email:
State:
County / Parish:
Province:
Prefix:
a. YES
b. NO
16. IS APPLICATION SUBJECT TO REVIEW BY STATE EXECUTIVE ORDER
12372 PROCESS?
I agree
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DATE:
THIS PREAPPLICATION/APPLICATION WAS MADE
AVAILABLE TO THE STATE EXECUTIVE ORDER 12372
PROCESS FOR REVIEW ON:
PROGRAM HAS NOT BEEN SELECTED BY STATE FOR
REVIEW
PROGRAM IS NOT COVERED BY E.O. 12372; OR d. Estimated Program Income
21. Cover Letter Attachment Add Attachment Delete Attachment View Attachment
14. PROJECT DIRECTOR/PRINCIPAL INVESTIGATOR CONTACT INFORMATION
I. Hypothesis and Specific Aims: The objective of this project is to demonstrate new
methods regarding studies done previously and to work on patient care quality, which is a
common challenge in the sector of health. The aims that the study aims to accomplish are:
A. To increase patients’ safety by using initiatives that are relevant.
B. To implement innovations in the patient’s health care sector.
II. Methodology
A. Study Design
The type of study design that will be used is the cross-sectional study which will include
follow-ups to assess the effects of increasing the safety of patients and innovations in
healthcare. Through follow-ups studies, the results will be more successful.
B. Sample selection
The study will take place in California, United States of America. The individuals to
participate in this study are in-patients and outpatients in Cedars-Sinai Medical center of
15 years and above. A total of 72 patients will be involved in this study.
C. Data Collection
The data will be collected through interviews, observations and questionnaires. The
patients will be given templates with questions regarding the type of care they are facing
and if they are satisfied with it. Moreover, they would be asked to provide suggestions on
how the quality of care they receive can be improved. Observations on how nurses,
doctors and other medical staff care for their patients to find out on what sectors need
improvements.
D. Data Analysis
The data collected from the respondents will be analyzed using the qualitative content
method of analyzing data. Frequencies in which complaints have been said or written by
patients regarding the type of care received will be critically analyzed. Also, suggestions
regarding improvement techniques will be key in analyses. Lengthy or large amounts of
responses will be grouped in codes and summarized into themes and categories, and get
tabulated.
III. Ethics
A. Protection of human subjects
Interests and welfare of the humans that will be involved in this research will be key
in order to reduce the chances of offending them or of risk occurrence. Any risks that
may occur during the research will be assessed, and the steps that are required to
protect the subjects from the risks will be carried out effectively before the beginning
of the research.
B. Consent and confidentiality
The data provided by one respondent will be very confidential for any other
respondent or person apart from the researcher to see. The interview will be carried
out in turns and privately to avoid disclosing information that may be very
confidential to a participant. The questionnaire filled documents will be locked in
secure places.
C. Data sharing
The data obtained from this research will be shared with other researchers. This will
be done through a qualitative method whereby codebooks, transcripts and interview
guides will be used in order to make it possible for others to verify claims rationales
in a certain qualitative study and also to yield new insights.
IV. Timeline
The study will be conducted for a period of one month which is enough to collect all the
necessary information on the possible ways to improve the care provided to patients. The
first week will involve preparation for the study and assembling all the required
materials, and visiting the study site to plan on how the research will be conducted. The
third week will involve information collection and the final week is when data will be
compiled and the results analyzed.
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