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CONSENT FORM SCREENING VISIT Title:Prevention of Type 2 Diabetes amongst South Asians with central obesity and prediabetes (iHealthT2D) REC Ref: 182806, Screening Version 1, March 2016 Researchers:
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The participant information sheet v1 is a document that collects essential details about individuals participating in a study or program, ensuring proper data management and ethical compliance.
Researchers, organizations, or institutions conducting studies that involve participant interaction or data collection are required to file the participant information sheet v1.
To fill out participant information sheet v1, individuals need to provide accurate demographic information, consent, and any required personal or health-related details as specified in the guidelines.
The purpose of the participant information sheet v1 is to inform participants about the study, ensuring they understand their role, rights, and the use of their data, thereby facilitating informed consent.
The participant information sheet v1 must report information such as participant demographics, study details, consent options, and any potential risks or benefits associated with participation.
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Relevant keywords

2016 ihealth t2d iras anonymised v1 prediabetes uk jaspal kooner pct nhs analyses gp satisfactorily incapacity arising obesity asians prevention anonymously databases modification relinquish researchers deposited medically resulting relevance rec

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