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Bryant et al. BMC Cancer (2015) 15:295 DOI 10.1186/s128850151314xSTUDY Protocolize AccessProtocol of a multigenre randomized controlled trial of a web based information intervention with nurse delivered
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01
Start by clearly defining the objectives and purpose of the multi-centre protocol.
02
Identify all the participating centres and obtain their consent to be part of the study.
03
Develop a structured format for the protocol, including sections for background, study design, inclusion and exclusion criteria, data collection and analysis, ethical considerations, etc.
04
Provide detailed instructions on how to complete each section of the protocol, ensuring consistency and accuracy.
05
Clearly outline the roles and responsibilities of the investigators at each centre.
06
Include a section for obtaining necessary approvals from ethics committees or regulatory bodies.
07
Specify the timeline for the study, including recruitment, data collection, and analysis.
08
Hold regular meetings with all participating centres to address any questions or concerns regarding the protocol.
09
Provide templates or examples of completed protocols to help centres in filling out their own protocols.
10
Review and revise the protocol as needed based on feedback from the centres and external reviewers.

Who needs protocol of a multi-centre?

01
Researchers or organizations conducting multi-centre studies
02
Ethics committees or regulatory bodies reviewing multi-centre study proposals
03
Investigators and study coordinators involved in multi-centre studies
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The protocol of a multi-centre is a document outlining the procedures and guidelines for a research study conducted at multiple centers.
The principal investigator is usually required to file the protocol of a multi-centre.
The protocol of a multi-centre should be filled out following the specific guidelines provided by the research institution or regulatory body.
The purpose of the protocol of a multi-centre is to ensure standardized procedures are followed across all centers involved in the research study.
The protocol of a multi-centre must include details about the study objectives, methodology, participant selection criteria, data collection procedures, and ethical considerations.
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