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7. Participant Retention 7.1 Overview of Section 7 This section presents information related to participant retention definitions, requirements, and procedures. Once a participant enrolls in HP TN
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01
Familiarize yourself with the purpose of participant retention in the context of the HPTN (HIV Prevention Trials Network) study.
02
Ensure you have access to the necessary data and information regarding the participants in the study.
03
Identify the key factors that can influence participant retention, such as communication strategies, incentives, and support systems.
04
Develop a comprehensive plan for participant retention that is tailored to the specific needs of the study.
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Implement the plan, keeping track of the progress and effectiveness of the strategies used.
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Regularly evaluate and reassess the participant retention efforts to make necessary adjustments and improvements.

Who needs participant retention - hptn?

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Researchers and coordinators involved in the HPTN study require participant retention to ensure the statistical validity and reliability of the findings.
02
Participants who have enrolled in the study benefit from participant retention efforts as it helps maintain their involvement and engagement in the research.
03
Funders and sponsors of the HPTN study are interested in participant retention as it ensures the successful completion of the study and the delivery of valuable results.
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Participant retention in HPTN refers to the process of keeping participants engaged in the clinical trial from enrollment to completion.
All sites and researchers involved in the HPTN trial are required to submit participant retention data.
Participant retention data for HPTN can be filled out through the designated online portal provided by the trial organizers.
The purpose of participant retention in HPTN is to ensure the integrity and success of the clinical trial by maintaining participant involvement.
Participant retention data for HPTN typically includes information on participant follow-up visits, study completion status, and any reasons for discontinuation.
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2015 HPTN HIV SDMC IRB IoR Statistician DAIDS offsite registries evaluable QA timeframes CRMs QC ECs IRBs designee enrolls multifaceted SSP caseloads minimally allowable newsletters attainable judicious directories implementation maximizing enrolling

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