Introduction

My name is Frank Castel, and I am currently pursuing a Masters degree in nursing at Regis College. According to the institution’s guidelines, I am required to undertake outstanding research that will improve the present information in nursing to make the profession more competent. From this, I have designed, and I am currently developing an experimental study. The primary objective of the study is to investigate what physical injuries nurses experience when handling for obese and pregnant patients.

This template is a formal invitation for your participation in the study. However, it should be noted that it is voluntary. This means that even if one has signed up for the survey, they may leave at whatever point as indicated in the informed consent that will be filled.

Eligibility for study participation requires the subject to be a nurse (does not indicate the level of professionalism) and should be above the age of 21 years of age.

Procedure

The participant is required to fill out a questionnaire as well as answer impromptu questions regarding the objective of the study (Kim & Miller, 2015). In exceptional circumstances, group study will be conducted which ensures participant interaction which will boost the study’s primary objective. When possible, further appointments will be set out to present more relevant information if the researcher is not satisfied with the provided ones at the moment.

Potential Benefits

The benefits are targeted at improving the current knowledge of physical injuries experienced by nurses while caring for specific types of patients. It is believed it will open up an avenue where detailed research would be conducted and essential discovery of measures for each example of care.

Potential Risks

There are no potential risks associated with the present study. But, at a minimal point, chances are associated with information biasness, and this may hinder the credibility of the research.

Cost

Costs incurred will be by the researcher, not the participant.

Right to Refusal/ Withdrawal of Participation

Participants should know that the study is on a voluntary basis and the participant can leave whenever they desire.

Assurance of Privacy and Confidentiality

Personal information will not be used disclosed. Participants will only fill in professional details and each provided with an identity number (Spatz et al., 2016). Data will be stored in secure computers and files with authorized entry codes.

Additional Information

At any one point, if the participant has any question or concern, they may contact the researcher with the provided details (Trung et al., 2017). Any concerns should be directed to the Chairperson of Regis College Institute. The details of the Chairperson are provided below including the name and the telephone number. The participants will be presented with the documents that require confirmation of participation and acknowledgment of the knowledge about the study.

Research Participant

By signing below, you agree that you have read the above document, been provided with the opportunity to ask questions where necessary and understood the risks associated with the study. Also, as the participant, you are aware of the voluntary state for participation.

Name: ____________________________________________________________________

Participant Signature: ____________________________________________________-

Date: ______________________________________________________________________

Individuals Conducting Research Signatures:

I have explained the details of the research and have answered all the questions regarding the study to the best of my ability.

Signature _______________________________________

Date: __________________________________________

IRB Approval

This form has been approved by the Regis College IRB

Authorising Signature: ___________________________________________

Date: ________________________________________________________

References

Kim, S. Y., & Miller, F. G. (2015). Informed consent for pragmatic trials: the integrated consent Model.

Spatz, E. S., Krumholz, H. M., & Moulton, B. W. (2016). The new era of informed consent: getting to a reasonable-patient standard through shared decision making. Jama, 315(19), 2063-2064.

Trung, L. Q., Morra, M. E., Truong, N. D., Turk, T., Elshafie, A., Foly, A., … & Ngoc, T. N. (2017). A systematic review finds underreporting of ethics approval, informed consent, and incentives in clinical trials. Journal of clinical epidemiology, 91, 80-86.

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