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Resilience Skills SelfManagement for Chronic Pain (PRISM Study) NCT03304613 Date: 3/17/2021Study ID: HUM00124722 IRB: IRBMED Date Approved: 3/17/2021 Expiration Date: 2/16/2022UNIVERSITY OF MICHIGAN
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01
Ensure you have all necessary patient information and consent forms ready.
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Prepare the study protocol and obtain approvals from the relevant ethics board.
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Recruit participants based on the inclusion and exclusion criteria outlined in the protocol.
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Collect baseline data from participants before the intervention begins.
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Implement the intervention as described in the study protocol.
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Monitor participants throughout the study for any adverse effects or complications.
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Collect follow-up data at the specified time points involved in the study.
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Perform data analysis once all data is collected and ensure results are documented.
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Prepare a report of findings and submit for publication or presentation.
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What is pilot single center open?
Pilot single center open refers to a type of clinical trial or research study conducted at a single location, focusing on evaluating a specific intervention or treatment.
Who is required to file pilot single center open?
Researchers or organizations conducting a pilot single center open study are required to file the necessary documentation with relevant regulatory bodies.
How to fill out pilot single center open?
To fill out a pilot single center open form, ensure you include relevant study information, participant details, and any specific data requested by the regulatory authority.
What is the purpose of pilot single center open?
The purpose of a pilot single center open study is to assess the feasibility, time, cost, risk, and adverse events involved in conducting a full-scale trial.
What information must be reported on pilot single center open?
Reported information typically includes study objectives, methodology, participant demographics, intervention details, and outcomes measured.
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