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NCT03892967Enhanced, Facilitated Cancer Symptom Control (E2C2) Pragmatic Clinical Trial June 26, 2020Minimal Risk Protocol Template [IRB 10429.010]Effective: 9/20/2017IRB Minimal Risk Protocol Template

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How to fill out minimal risk protocol template

01

Start by providing a clear title for the protocol.

02

Include a brief introduction explaining the purpose and significance of the study.

03

Detail the research methods and procedures to be used in the study.

04

Describe the potential risks and how they will be minimized.

05

Provide information on how subjects will be recruited and consented.

06

Include a section on how data will be collected, stored, and analyzed.

07

Outline the qualifications and roles of individuals involved in the study.

08

Conclude with any additional information or considerations relevant to the study.

Who needs minimal risk protocol template?

01

Researchers conducting studies involving minimal risk to participants.

02

Institutional review boards (IRBs) or ethics committees reviewing research protocols.

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What is minimal risk protocol template?

The minimal risk protocol template is a standardized form that outlines the procedures and precautions to be taken when conducting research with minimal risk to participants.

Who is required to file minimal risk protocol template?

Researchers and institutions conducting studies with minimal risks are required to file the minimal risk protocol template.

How to fill out minimal risk protocol template?

The minimal risk protocol template can be filled out by providing information on the study design, participant population, procedures, and risk mitigation strategies.

What is the purpose of minimal risk protocol template?

The purpose of the minimal risk protocol template is to ensure that studies with minimal risk are conducted ethically and with participant safety in mind.

What information must be reported on minimal risk protocol template?

The minimal risk protocol template must include details on the study objectives, methodology, participant inclusion criteria, informed consent process, and risk management plan.

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