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Example of Electronic Invitation Letter
Invitation to Participate in Research Study
A Correlational Study of Childhood Religiosity, Childhood Sport Participation, and Sport-Learned Aggression Among African American Female Athletes
Participants are needed for a research study in order to gain insight on the relationships among childhood religiosity, childhood sport participation, and sport-learned aggression. The research cannot be performed without data. Your participation is voluntary and provides that data. Your name will not be written on the questionnaires. The survey site will be active for three weeks.
You are being invited to participate in this study because you are a member of Zoomerang and because you match the characteristics
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Although the results of the research study will be published, your name or identity will not be revealed. The health information provided in the research study will be used by the researcher as a way to control extraneous variables. This information may be confirmed by members of the dissertation committee.
The researcher is required by law to protect your health related information. By electronically signing this document, you authorize the researcher to use and/or disclose your health related information for this research. Those individuals who receive your health related information may not be required by Federal privacy laws to protect the information and they may share it with other people without your permission, if permitted by the laws that govern them.
This authorization has no expiration date. However, you may voluntarily withdraw from the study at any time prior to electronically submitting the data. Once the data are collected, it will no longer be possible to link the data to the signed confidential health care information forms. Please click on the appropriate box below that indicates whether you would like to participate in this study or whether you want to withdraw from this
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Purpose
The purpose of this study is to determine the relationships among childhood religiosity, childhood sport participation, and sport-learned aggression. However, other variables may affect the study. Some of them will be controlled by design. Others will be assessed in the demographics part of the survey.
III. Participation
About 500 females have been invited to participate in this study. You have been selected because you represent the study’s population. You are an African American female. You are 21 to 40 years of age. You have not been medically treated for depression. You have not been diagnosed with ADD.
Participation is voluntary. You do not have to participate in this study. Nothing will happen to you if you do not want to participate in this study. If you have any questions involving this study, you may call the researcher at xxx-xxx-xxxx.
IV. Procedures
The study will take a total of about 20 minutes to complete. You will mark your answers by clicking on the best response. You will then submit the completed survey online to Zoomerang.
V. Reason for Participation
You have been asked to participate in this study in order to provide data. The data will be used to gain insight on the relationships among variables. The research cannot be performed without data. Your participation provides the needed
The flip side of the signing a confidentiality document under HIPAA policy healthcare officials many times has been frustrated because bounds they can’t cross. Many times family or friends who aren’t authorizes obtains valuable medical information are coming all hours of the day to ask for critical medical reason, the nurses, physicians and others officials bid my law not to get out information on the telephone, or in personal if the individual or individuals name aren’t on the privacy document. Having a ...
The IRB is an administrative body which has been established to make sure research participants' rights are protected. IRBs review all aspects of the researchers' project: the study design, the recruitment process, the participant population, the informed consent document and process, the risk/benefit ratio, privacy and confidentiality, data storage and protection, and safeguards for vulnerable participants (University of St. Francis, n.d.). In this way, participants' rights are protected because the effort is made even before the research begins. The review process ensures that participants are chosen fairly and informed adequately and the information collected during research is safeguarded through collection, use, and storage. Research using human participants is such an important part of medicine that it is imperative it is performed in a way that its intrigue is not compromised.
The guidance explains and clarifies key provisions of the medical privacy regulation, which was published last December (HIPAA, 1996). Guaranteeing the accuracy, security, and protection of the privacy of all medical information is crucial and an ongoing challenge for many organizations. References American Medical Association (2005). Retrieved December 7, 2008, from http://www.ad http://www.ama-assn.org/.
Researchers who conduct interventional clinical research have put into question the Privacy Rule and how it will affect their research activities. The Department of Health and Human Services, Food and Drug Administration and Protection of Human Subjects Regulations are advised to take measures to protect the
With today's use of electronic medical records software, information discussed in confidence with your doctor(s) will be recorded into electronic data files. The obvious concern is the potential for your records to be seen by hundreds of strangers who work in health care, the insurance industry, and a host of businesses associated with medical organizations. Fortunately, this catastrophic scenario will likely be avoided. Congress addressed growing public concern about privacy and security of personal health data, and in 1996 passed “The Health Insurance Portability and Accountability Act” (HIPAA). HIPAA sets the national standard for electronic transfers of health data.
.In addition young athletes have become more aggressive. Kids that participate in competitive sports are becoming more and more aggressive and competitive the sports have become themselves. Mitchell reveals "traits like bullying and the need to dominate their oppo...
Protecting Personal Health Information in Research: Understanding the HIPAA Privacy Rule, NIH Publication Number 03-5388. Retrieved November 12, 2011 from http://privacyruleandresearch.nih.gov/pr_02.asp
HIPPA Privacy Rules were established to protect health information that may be used or disclosed by covered entities for research trial purposes. HIPPA Privacy Rules define research as a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalized knowledge (“Research,” HHS.gov, June 5, 2013). Privacy Rule established regulation guidelines to inform research volunteers on how medical information for research purposes will be utilized. Guidelines and right to access medical information held by researching entity are also covered in the HIPPA Privacy Rule. Countermeasures to establish protection of identifiable individual health information during research are extremely important,
Introduction: Health information is regarded as one of the most sensitive types of personal information. For this reason, the Privacy Act 1988 provides extra protections around its handling. For example, a counselling organisation generally needs a client’s consent before they can collect their health information. The Privacy Act regulates how organisations collect and handle personal information, including health information. It also includes provisions that generally allow a person to access information held about them.
The confidentiality of personal health information is an issue that affects every American. Secretary Donna E. Shalala, PhD from the U.S. Department of Health and Human Services quoted, "Will our health records be used to heal or reveal us?" AHIMA, a professional...
For the interviews two individuals who self-identify as African-American/Black were recruited. The individuals were previously known by the researcher and were not compensated for their assistance. The interviews were semi-structured in nature and some questions had been previously prepared and they are found on Appendix A. One interview took place through Facebook chat and the second interview took place outside of the UCI Starbucks near the Student Center and lasted approximately 45 minutes.
Privacy challenges. Privacy is a circumstance of restricted right of entry to an information regarding an individual (Knoppers, 2015). Brothers and Rothstein (2015) noted numerous other kinds of privacy, comprising physical, decisional, proprietary and relational or associational privacy. This study emphasizes on informational health privacy. When it comes to privacy issues the crucial question to explore is; how can leadership balance the right of privacy with the advantageous requirement for clinical data-access in EHR? The Privacy Act of 1974 is the US law that represents national standards to protect the private health information of individuals by mandating appropriate safeguards and limitations on the right to use and release of (PHI)
The questionnaire encompasses five sections. The first section is an introduction. The aim of the research and the completion time of the questionnaire were introduced in the section and make sure the respondents know the security of the information they offered. The second section included only two demographic questions, which are ‘What is your gender?’ and ‘How old are you?’
Linver, M. R., Roth, J. L., & Brooks-Gunn, J. (2009). Patterns of adolescents' participation in organized activities: Are sports best when combined with other activities? Developmental Psychology, 45(2), 354-367. doi:http://dx.doi.org/10.1037/a0014133
Individual privacy and confidentiality play a role in both research and clinical health care settings. In each instance, standards and expectations put in place by researchers and health care practitioners to follow to protect patients and research participants while interacting with them. The evolving health care system and convergence of research and treatment protocols to create learning health care systems (LHCS) are creating the need to look at patient confidentiality and privacy differently to protect them and their information.