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Supporting Women with Postnatal Weight Managements Feasibility Trial PROTOCOLV7. August 13thth 2017 IRAS No. 179204A two arm feasibility ACTs of lifestyle information and Slimming World groups to
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Start by writing the title of the protocol, indicating that it is for a two-arm study.
02
Provide a brief introduction to the study and the rationale behind it.
03
Clearly outline the objectives and aims of the study.
04
Describe the study design and methodology, including information on the two arms and how participants will be assigned to each arm.
05
Specify the inclusion and exclusion criteria for participant selection.
06
Explain the interventions or treatments that will be administered to each arm.
07
Discuss the outcome measures that will be assessed and how data will be collected.
08
Provide details on sample size calculation and statistical analysis plan.
09
Outline the ethical considerations and any necessary approvals obtained.
10
Clearly mention the expected timeline and milestones of the study.
11
Include any additional information or instructions relevant to the study.
12
Proofread and revise the protocol to ensure clarity and coherence.

Who needs protocol for a two-arm?

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Protocols for two-arm studies are needed by researchers, clinicians, and scientists conducting clinical trials or experimental research comparing two different interventions or treatment strategies. These protocols serve as a blueprint for the study and provide detailed instructions on the study design, methodology, and data collection procedures. They are essential for ensuring the study is conducted in a systematic and ethical manner, and for facilitating collaboration among research team members.
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Protocol for a two-arm is a detailed plan outlining the design, methodology, and objectives of a clinical trial with two treatment groups.
The principal investigator or sponsor is required to file protocol for a two-arm clinical trial.
Protocol for a two-arm is typically filled out by providing information on study design, inclusion and exclusion criteria, endpoints, statistical analysis plan, and ethical considerations.
The purpose of protocol for a two-arm is to ensure the safety of participants, maintain scientific integrity, and guide the conduct of the clinical trial.
Protocol for a two-arm must include details on study objectives, eligibility criteria, study procedures, data collection, safety monitoring, and statistical analysis plan.
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