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INFORMATION SHEETTitleRandomised control trial of standalone resistance training in people with Chronic Psychotic DisordersCoordinating Principal Investigator Dr Nicole KormanPrincipal Investigator
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What is Participant Ination Leaflet and Ined Consent Form?

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A participant information leaflet is a document that provides participants in a research study or clinical trial with information about the study's purpose, procedures, risks, benefits, and their rights as participants.
The researchers or institutions conducting the study are required to file the participant information leaflet as part of the ethical and regulatory approval process for the research.
To fill out a participant information leaflet, ensure that it includes clear language explaining the study's objectives, methods, potential risks, and benefits, as well as instructions for participants on how to proceed if they agree to take part.
The purpose of the participant information leaflet is to inform potential participants about the study details and to ensure that they can make an informed decision about their participation.
The leaflet must report information such as the study's purpose, duration, procedures involved, potential risks and benefits, confidentiality of data, and whom to contact for questions.
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