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Study of Home-Embedded Palliative Care for Hemodialysis-Dependent End-Stage Renal Disease (SHEPHERD)

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University of Pennsylvania

Status

Completed

Conditions

End-Stage Renal Disease

Treatments

Behavioral: Nudge for PHPC Referral

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Home palliative care needs are often under-recognized in patients with End-Stage Renal Disease (ESRD). This pilot study is designed to evaluate the feasibility and acceptability of an initiative to enhance referrals to Penn Home Palliative Care compared with usual care among hemodialysis-dependent ESRD patients admitted to a Penn hospital. Results will inform a future pragmatic trial comparing the effectiveness of home palliative care compared with usual care among ESRD patients. Evaluating the effectiveness of home palliative care services is critical to determine whether increasing access to these services would improve patient-centered outcomes for these high-need patients.

Enrollment

285 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Be an adult (18 years of age or older) hospitalized at one of two study hospitals

  • Digital signature of ESRD (N18.6) within the last 12 months with an inpatient hemodialysis order

  • Patient resides in the five-county area surrounding Philadelphia which is served by the Penn Home Palliative Care services.

  • Appropriate for home palliative care, defined as:

    (i) Existing home care eligibility/referral for home care OR (ii) Severe protein malnutrition (E43, E44) OR (iii) Non-ambulatory status determined by a flowsheet completed by nursing on hospital admission with three ambulatory options: (1) non-ambulatory, (2) ambulates with assistance, or (3) ambulates independently. If this information is missing from the electronic health record, the determination will be made using one of the three following options: (1) overall prior home mobility assessment "complete dependence on all aspects," or (2) ambulation or functional transfers domains indicate "dependent," or (3) wheelchair mobility domain was completed (with any non-null/non-empty value).

Exclusion criteria

  • None

Trial design

Primary purpose

Health Services Research

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

285 participants in 2 patient groups

Intervention
Experimental group
Description:
The lead case manager and covering provider on the inpatient care team for participants in this group will receive a message from the research team identifying their patient as appropriate for home palliative care and will be asked to refer their patient for these services.
Treatment:
Behavioral: Nudge for PHPC Referral
Usual Care
No Intervention group
Description:
Participants in this group will receive usual care upon discharge from the hospital. Their clinical team will not be notified that they are appropriate for home palliative care services, but they may still be referred for those services if their clinicians feel their patient will benefit.

Trial contacts and locations

1

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Central trial contact

Vanessa Madden, MS, MPH; Nicholas Bishop

Data sourced from clinicaltrials.gov

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