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ADAPTED HARVARD TRAUMA QUESTIONNAIRE WITH PTSD CIVILIAN CHECKLIST 5Indian Version Name/ID: ___ Sex: ___ Date of Birth: ___ Marital Status: ___ Date: ___Weathers, F.W., Liz, B.T., Keane, T.M., Palmier,
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01
Identify the objectives and goals of the pilot study adaptation.
02
Review the original study design and protocol.
03
Determine if any modifications are needed to the study procedures or data collection methods.
04
Obtain any necessary approvals from regulatory bodies or ethics committees.
05
Recruit participants for the pilot study.
06
Conduct the pilot study according to the adapted protocol.
07
Collect and analyze data from the pilot study.
08
Evaluate the results and make any necessary adjustments to the study design before proceeding to the full study.

Who needs a pilot study adapting?

01
Researchers who are planning to conduct a larger study and want to test and refine their methods before scaling up.
02
Research teams working on complex studies that require multiple iterations to optimize study protocols.
03
Funding organizations that want to ensure that their resources are used efficiently and effectively in larger studies.
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A pilot study adapting is a preliminary research study conducted before a larger research study to test the feasibility and effectiveness of specific methods or procedures.
Researchers or organizations conducting research studies that involve potential risks to human subjects or require approval from an ethics committee are required to file a pilot study adapting.
To fill out a pilot study adapting, researchers need to provide details about the research objectives, methodology, potential risks to participants, informed consent procedures, and ethical considerations.
The purpose of a pilot study adapting is to identify and address any potential issues or challenges that may arise in a larger research study, improve the research methodology, and ensure the safety and well-being of participants.
Information that must be reported on a pilot study adapting includes the study objectives, methodology, potential risks to participants, informed consent procedures, ethical considerations, and any preliminary results.
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