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Open accessProtocolHORIZONS protocol: a UK prospective cohort study to explore recovery of health and wellbeing in adults diagnosed with cancer Claire Foster,1 Lynn Cayman,1 Alison Richardson,1 Carl
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To fill out a UK Prospective Cohort, follow these steps:
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Collect the necessary data such as demographic information, lifestyle factors, medical history, and other relevant information of the participants.
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Determine the inclusion and exclusion criteria for the cohort study to ensure the participants meet the required criteria.
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Develop a data collection form or questionnaire to record the collected information.
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Recruit participants who meet the inclusion criteria from the target population.
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Provide clear instructions to the participants on how to complete the data collection form or questionnaire.
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Ensure the confidentiality and privacy of the collected data, while also obtaining necessary consent from the participants.
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Regularly monitor and follow up with the participants to track any changes in their health status or other relevant factors.
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Conduct data analysis using appropriate statistical methods to draw meaningful conclusions from the cohort study.
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Publish and disseminate the findings of the cohort study to contribute to scientific knowledge and inform public health interventions.
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Continually update and maintain the cohort study dataset for long-term follow-up and future research purposes.

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A UK prospective cohort is a study that follows a group of individuals over a period of time to observe their behavior, health outcomes, or other factors.
Researchers, scientists, or institutions conducting the cohort study are required to file a UK prospective cohort.
To fill out a UK prospective cohort, researchers need to provide detailed information about the study design, objectives, participants, methods, and expected outcomes.
The purpose of a UK prospective cohort is to gather valuable data over time to understand the development of diseases, health behaviors, or other relevant outcomes.
Researchers are required to report information such as participant demographics, study protocols, data collection methods, and any relevant findings.
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