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Clinical Trial Summary

The purpose of this study is to estimate the potential benefit of early and continued palliative care (PC) consultation on end of life issues.


Clinical Trial Description

Participants in this study will be randomized to either an intervention group or a standard of care group. Participants in the intervention group will participate in regular visits with a palliative (or supportive) care specialist, while participants in the standard of care group will only see palliative care specialists if the clinician requests a referral. All participants will be asked to complete monthly questionnaires regarding their general well-being. Participants have a greater chance of being assigned to the intervention group than to the standard of care group. On average, in every 5 people randomized, 3 will be randomized to the intervention and 2 will be randomized to standard of care. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04482894
Study type Interventional
Source University of Virginia
Contact Emily Leytham
Phone (434) 924-7621
Email EL5MF@hscmail.mcc.virginia.edu
Status Recruiting
Phase Phase 2
Start date August 19, 2020
Completion date April 1, 2025

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