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ProtocolStudy protocol: an investigation of the prevalence of autism among adults admitted to acute mental health wards: a cross sectional pilot study Sam Romans , 1,2 Guiding Lily Lao,1 Reza King,1,2
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Step 1: Start by identifying the objective and purpose of the study protocol
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Step 2: Include a clear title and abstract that summarizes the study
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Step 3: Provide a detailed introduction to the research topic and background
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Step 4: Clearly define the research question and hypothesis
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Step 5: Describe the study design and methodology to be used
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Step 6: Specify the inclusion and exclusion criteria for participants
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Step 7: Outline the data collection methods and tools to be used
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Step 8: Explain the statistical analysis plan for the study
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Step 9: Address any ethical considerations and obtain necessary approvals
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Step 10: Create a timeline for the study activities and milestones
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Step 11: Include a budget and resource allocation plan
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Step 12: Discuss the potential risks, limitations, and challenges of the study
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Step 13: Ensure the protocol is reviewed by all relevant stakeholders
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Step 14: Revise and finalize the study protocol before implementation

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A study protocol is a detailed plan that outlines the objectives, design, methodology, statistical considerations, and organization of the study. It serves as a guide to ensure the study is conducted ethically and scientifically.
Researchers or organizations conducting studies, particularly those involving human or animal subjects, are typically required to file a study protocol with institutional review boards or relevant regulatory bodies.
To fill out a study protocol, researchers should follow a structured format that includes sections such as introduction, objectives, methods, data analysis, and ethical considerations. Each section should provide clear and concise information pertinent to the study.
The purpose of a study protocol is to ensure that the research is carried out consistently and according to ethical and legal standards. It helps to protect the rights and welfare of participants and provides guidelines for data collection and analysis.
Key information that must be reported includes the study title, objectives, methodology, participant criteria, timeline, funding sources, and any potential conflicts of interest.
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