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About
A small pilot study to assess feasibility and acceptability of the PL4Y intervention.
Full description
After completing enrollment and informed consent, participants will be randomly assigned to PL4Y in a 2:1 fashion (intervention:control) with a target enrollment of 40 receiving the intervention and 20 in the control arm for a total of 60 participants. There is no blinding in this study protocol.
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30 participants in 2 patient groups
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Central trial contact
Ruby Viera Corral; Barbara Taylor, MD, MS
Data sourced from clinicaltrials.gov
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