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Clinical Trial Summary

A small pilot study to assess feasibility and acceptability of the PL4Y intervention.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05689515
Study type Interventional
Source The University of Texas Health Science Center at San Antonio
Contact
Status Active, not recruiting
Phase N/A
Start date February 2, 2023
Completion date July 2025