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Template for RIH Assessment 3

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Added on: 2024-11-22 07:00:25
Order Code: SA Student Josephine Medical Sciences Assignment(9_23_36728_522)
Question Task Id: 495335

Template for RIH Assessment 3

Ethics application form

Refer to assessments 1, 2 and assessment 3 part 1 to complete the form. Answers should be coherent and consistent with your research proposal.

Refer to the subject module and to The National Statement on Ethical Conduct in Human Research

https://www.nhmrc.gov.au/about-us/publications/national-statement-ethical-conduct-human-research-2007-updated-2018#toc__1114).

The template is an abbreviated template for the purpose of the assessment 3 (Part 2) and should not be used for any other purpose.

Project Overview

Project Title:

Question 1.

Q1.1 Provide a concise summary of the research project that includes research aims, methodology, design, sampling approach, sample, the process of recruitment data collection, management and analysis. An appropriate statement regarding the following: validity rigor trustworthiness should be included. (200 words):

2. Participant Specific Questions

The following questions (2.1-2.2) require short answer responsesP2.1 How will the people participate in this research? (100 words)

2.2. Explain how the research is likely to advance knowledge about the health or welfare or other matters relevant to participants (100 words)

Consent Questions

Tick the most appropriate response to question 2.3-2.4

Q2.3 Which type of consent will you be obtaining from participants to participate in the research?

Informed verbal and written consent

Informed written consent

Informed verbal consent (recorded)

Waiver of consent

Informed implied consent (such as completion of an online questionnaire)

Other (specify)

Q2.4 From whom are you obtaining consent?

The participant

The children or young persons themselves

One parent

Both parents

The guardian or primary care giver

An organisation required by lawWaiver of consent

3. Risk and Benefits Questions

The following questions (3.1-3.3) require that you critically assess and discuss the risks and benefits of your proposed research.

Q 3.1 Describe the risks and burdens to potential participants that are associated with your research, referencing any relevant sections of your Project Description as appropriate and referring to the NHMRC guidelines (100 words)

Q 3.2 Describe how you will mitigate and manage the risks (100 words)

Benefit Questions

Q3.3 In 150 words, justify the benefits to undertake your research and the significance of the proposed research in regard to your research question and implications for practice such as

healthcare practice/policy or service delivery

public health practice/policy

healthcare facilities

broader population

Data and Privacy

Data Characteristics and collection, and storage

Tick the most appropriate response for your study

Q4.1 Indicate the type of information/data you will be collecting for this project.

Personal information

Sensitive information

Health information

Not personal information

Q4.2 Indicate the type of information/data you will be using in this project:

Personal information

Sensitive information

Health information

Not personal information

Q4.3 Indicate the degree of identifiability of information/data you will be collecting for this project.

Individually identifiable information

Re-identifiable (coded) information

Non-identifiable information

Q4.4 Indicate the degree of identifiability of information/data you will be using in this project.

Individually identifiable information

Re-identifiable (coded) information

Non-identifiable information

Q4.5 How will you protect the privacy of participants and their identity during data collection?

Activities Planned for/with DataRefer to NHMRC guidelines.

The following question (4.6) requires a short answer response (50 words)

Q4.6 How will you protect the privacy of participants in any notes and/or publications arising from your research?

The following question (4.7) requires a short answer response (50 words) to justify your Yes or No response.

Q4.7 Are there any restrictions on your ability to assure the confidentiality of participants?

Yes or No and why

The following question (4.8) requires a short answer response (50 words)

Q4.8 Describe how the information/data will be stored, and accessed

The following question (4.9) requires a short answer response (50 words)

Q4.9 Describe any ethical considerations relating to the storage of, access to or destruction of information/data in this project

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