CClinicalTrials.gg
Active, not recruitingNCT04071951Updated Apr 2, 2026Results posted

Pharmacist Intervention to Reduce Post-Hospitalization Utilization

An interventional study of Pharmacist-led Hospital Discharge Care Intervention in Nonadherence, Patient, Polypharmacy and Readmission, sponsored by Cedars-Sinai Medical Center. Active, not recruiting at 2 sites in United States. Open to participants aged 55 Years and older. Per ClinicalTrials.gov, last updated 2026-04-02.

Sponsored by Cedars-Sinai Medical Center · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
6,478
Allocation
Randomized
Ages
55 Years and older
Sex
All
01

Study summary

This is a randomized trial testing a peri- and post-discharge pharmacist-led medication management intervention on post-discharge utilization, including both readmissions and emergency department visits within 30 days of discharge. The intervention incorporates evidence addressing three main areas: medication reconciliation, medication adherence, and polypharmacy.

This study uses a pragmatic trial randomized at the patient level and conducted in two large hospitals to achieve the following aims, each of which has been designed using the RE-AIM framework:

Aim 1: To test the effect of PHARM-DC on post-discharge utilization among patients most at risk for post-discharge ADEs: recently discharged older adults taking >10 medications or >3 high-risk medications using a prospective, randomized, pragmatic multi-site study.

Aim 2: To study barriers and facilitators of implementing PHARM-DC using a qualitative study.

Aim 3: To analyze the costs of PHARM-DC, including the incremental cost per readmission averted and the net incremental cost from the health system perspective using a time-and-motion study and a cost-effectiveness analysis.

Read the detailed description

There are three components to this study: (1) the prospective, randomized, controlled trial (RCT), which includes a pharmacist-led hospital discharge care intervention, (2) the qualitative study, which involves focus groups and interviews, and (3) a cost-effectiveness study, which involves a review of the literature and a time-and-motion study component.For all three studies, there are two sites: CSMC and Brigham and Women's Hospital in Boston. Additionally, Dr. Kennelty of University of Iowa will participate in the qualitative study.1. For the RCT: Eligible patients will be identified through the use of a daily Epic report using inclusion/exclusion criteria. Patients will be randomized by a study coordinator to the intervention arm or control arm. For the control arm, patients will receive usual care, which includes medication reconciliation at hospital admission. For the intervention arm, pharmacy staff will address medication reconciliation at hospital discharge, medication review, and medication adherence. Most intervention activities will occur during the hospital stay or during a post-discharge phone call. We estimate a total number of 4,888 patients per study arm.

2. For the qualitative study: This is a qualitative study employing focus groups aimed at understanding implementation barriers and facilitators. Dr. Kennelty and study staff will conduct 3-day site visits to hold focus groups and/or interviews regarding intervention expectations, how the intervention is being implemented, barriers/facilitators to adoption and implementation, and adaptations made during delivery. Towards the end of the trial, Dr. Kennelty and study staff will use phone interviews to determine any changes to the implementation of PHARM-DC that occurred during the RCT, as well as to understand whether and how institutions will address the maintenance of PHARM-DC after the study ends. We estimate that up to 180 people may participate in this qualitative study.

3. For the cost-effectiveness study: This is a time-and-motion study aimed at understanding how much time during the day pharmacists spend on activities related to the hospital discharge (and post-discharge) interventions. During the trial, we will use time and motion methodology to understand how much pharmacist time is needed for PHARM-DC. Coupled with data on post-discharge utilization, this will enable us to conduct economic analyses.

02

Conditions studied

  • Nonadherence, Patient
  • Polypharmacy
  • Readmission

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03

In context

Patient Compliance

114 studies on the registry are indexed under Patient Compliance; 38 are open to participants now.

This study's enrollment of 6,478 is above the median of 120 across 87 interventional studies indexed under Patient Compliance.

Browse Patient Compliance studies →

Lead sponsor

Cedars-Sinai Medical Center is the lead sponsor of 441 studies on the registry; 108 are open to participants now.

Of its 62 completed or terminated interventional studies of FDA-regulated products, 47 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
55 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Admitted to a medical ward, AND
  • > 55 years AND
  • ≥ 10 prescription medications at admission

OR

  • ≥ 3 high-risk medications (anticoagulants, antiplatelets, insulin, oral hypoglycemics) at admission

Exclusion criteria

Exclusion Criteria:

  • Expected discharge to another state, acute care facility, psychiatric facility, or locked facility (including locked skilled nursing facility, jail, or prison) OR
  • Expected AMA or left hospital against medical advice (AMA) OR
  • Homeless OR
  • On hospice OR
  • Already enrolled into study within the past year OR
  • Patients admitted by admitting or attending Primary Medical Doctors who have a specialty that is not Internal Medicine or Family Medicine OR
  • Expected to receive pharmacist-led peri- and post-discharge medication management regardless of the trial OR
  • Expected post-discharge setting not conducive to the studied medication management intervention (e.g. SNF, rehabilitation facility) OR
  • Patients admitted with a suspected or confirmed diagnosis of COVID-19.
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
6,478 participants (actual)

Study arms

  • Experimental
    Pharmacist Arm

    Pharmacist-Led Medication Reconciliation, Regimen Review, and Adherence and Literacy Assessment and Counseling

    Behavioral: Pharmacist-led Hospital Discharge Care Intervention

  • No intervention
    Usual Care

    Patients in this study will receive usual care. Clinically-indicated services, including pharmacist services, may be provided to control group patients.

Interventions

  • BehavioralPharmacist-led Hospital Discharge Care Intervention

    Pharmacists will address medication reconciliation, medication adherence, and polypharmacy issues as appropriate. Pharmacists will rely most on their prior training, but study investigators will also encourage the use of documentation templates with reminders, Beers list, deprescribing, motivational interviewing, the Medication Adherence and Literacy tool, and post-discharge phone calls. Pharmacists will assess patient needs and customize accordingly. All patients will receive one discharge counseling visit and one post-discharge phone call, but pharmacists will find that some patients need further phone calls, interventions, referrals, or other interactions. Some or all of the pharmacist activities may take place over the phone.

06

What researchers measure

Primary outcomes

  1. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Based on EHR Data and CMS Claims)

    A patient is readmitted to a hospital (including observation) or has an ED visit within 30 days of discharge (including all hospitals at least statewide), excluding foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations

    Time frame: Hospitalization to a hospital or ED visit within 30 days of discharge (checking at least all same state facilities)

Secondary outcomes

  1. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital)

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge, excluding foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge (including other facilities in the system using the same electronic health record instance)

  2. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Receipt of Different Intervention Components

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge. This outcome measure will analyze the outcome by whether patients received the intervention components (admission medication reconciliation, medication regimen review, actions to improve adherence, side effect management, drug level monitoring, discharge medication reconciliation, patient/caregiver education, motivational interviewing, post-discharge follow-up phone call, medication access, communication with PCP, communication with communication pharmacy, other). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  3. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Whether Patient Has a Diagnosis of Congestive Heart Failure at Admission

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has a diagnosis of congestive heart failure at admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  4. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital), Stratified by Whether Patient Has Three or More High Risk Medications (Anticoagulants, Antiplatelets, Insulin, Oral Hypoglycemics) Prior to Admission

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has three or more high risk medications (anticoagulants, antiplatelets, insulin, oral hypoglycemics) prior to admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  5. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital), Stratified by Whether Patient Has 10 or More Medications Prior to Admission

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has 10 or more medications prior to admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  6. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Study Site

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by study site. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  7. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Patient Medication Adherence and Literacy

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient medication adherence and literacy (as assessed by study pharmacists, in addition to using limited English proficiency as a proxy for low medication literacy). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  8. Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Quintiles of Patient Socioeconomic Status (Estimated Via Median Income of Home Census Tract)

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient socioeconomic status (estimated via median income of home census tract). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  9. Rate (%) of New BZR Discharge Prescriptions Among Patients Not Taking BZRs Prior to Admission

    A dichotomous variable for a new discharge prescription of BZRs among patients not taking BZRs prior to admission.

    Time frame: Patients not taking BZRs prior to admission

  10. Rate (%) of Increased BZR Dose Prescription Among Patients Taking BZRs Prior to Admission

    A dichotomous variable for an increased dose prescription among patients taking BZRs prior to admission.

    Time frame: Patients taking BZRs prior to admission

  11. Rate (%) of Post-hospitalization Fall-related Injuries as Healthcare Utilization (Hospitalization, ED Visits, Urgent Care Visits, or Office Visits)

    The investigators define post-hospitalization fall-related injuries as healthcare utilization (hospitalization, ED visits, urgent care visits, or office visits) due to fall-related injuries within 30 days of discharge of the index admission. The investigators will link Medicare claims data to trial data to track this outcome at the individual patient level.

    Time frame: Fall-related injuries within 30 days of discharge of the index admission

  12. Rate of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Stratified by Patient Age Groups

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient age groups. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  13. Rate of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Stratified According to Time Periods That Had Changes in the Intervention and Control Arms

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified according to time periods that had changes in the intervention and control arms. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  14. Rate of 30 Day Post Hospitalization in ED Visits (Same Hospital) Restricted to Medication-related Utilization

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge restricted to medication-related utilization. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

  15. Rate of 7 Day Post-discharge Hospitalization Medication-related Post-discharge Utilization.

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 7 days of discharge by hospitalization medication-related post-discharge utilization. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 7 days of discharge

  16. Rate (%) of 30-day Post-discharge Hospital Utilization With ED Visits, Observation Stays, and Inpatient Readmissions Counted Separately (Including Hospitals at Least Statewide).

    A patient is readmitted to a hospital under inpatient or observation status or has an ED visit within 30 days of discharge (including hospitals at least statewide). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to a hospital or ED visit within 30 days of discharge (checking at least all same state facilities)

  17. 30-day, All-cause Mortality After Hospital Discharge

    All-cause mortality rate and survival analysis through Day 30 after hospital discharge.

    Time frame: Death occurring within 30 days after hospital discharge

  18. Rate (%) of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Among Patients Who Were Enrolled and Received the Intervention, Compared to Patients Who Were Eligible Yet Not Enrolled During the Study Period.

    A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

    Time frame: Hospitalization to the same hospital or ED visit within 30 days of discharge

07

Results

Posted Oct 29, 2024

Participant flow

Participant flow — Overall Study
MilestonePharmacist ArmUsual Care
Started32393239
Completed32133215
Not completed2624

Outcome measures

PrimaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Based on EHR Data and CMS Claims)

A patient is readmitted to a hospital (including observation) or has an ED visit within 30 days of discharge (including all hospitals at least statewide), excluding foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations

Time frame:
Hospitalization to a hospital or ED visit within 30 days of discharge (checking at least all same state facilities)
Reported as:
Count of participants · Participants
Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Based on EHR Data and CMS Claims)
ParticipantsPharmacist ArmUsual Care
Rate (%) of 30-day Post-discharge Hospitalization and ED Visits (Based on EHR Data and CMS Claims)570593
SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital)

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge, excluding foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge (including other facilities in the system using the same electronic health record instance)

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Receipt of Different Intervention Components

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge. This outcome measure will analyze the outcome by whether patients received the intervention components (admission medication reconciliation, medication regimen review, actions to improve adherence, side effect management, drug level monitoring, discharge medication reconciliation, patient/caregiver education, motivational interviewing, post-discharge follow-up phone call, medication access, communication with PCP, communication with communication pharmacy, other). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Whether Patient Has a Diagnosis of Congestive Heart Failure at Admission

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has a diagnosis of congestive heart failure at admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital), Stratified by Whether Patient Has Three or More High Risk Medications (Anticoagulants, Antiplatelets, Insulin, Oral Hypoglycemics) Prior to Admission

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has three or more high risk medications (anticoagulants, antiplatelets, insulin, oral hypoglycemics) prior to admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital), Stratified by Whether Patient Has 10 or More Medications Prior to Admission

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by whether patient has 10 or more medications prior to admission. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Study Site

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by study site. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Patient Medication Adherence and Literacy

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient medication adherence and literacy (as assessed by study pharmacists, in addition to using limited English proficiency as a proxy for low medication literacy). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospitalization and ED Visits (Same-hospital) Stratified by Quintiles of Patient Socioeconomic Status (Estimated Via Median Income of Home Census Tract)

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient socioeconomic status (estimated via median income of home census tract). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of New BZR Discharge Prescriptions Among Patients Not Taking BZRs Prior to Admission

A dichotomous variable for a new discharge prescription of BZRs among patients not taking BZRs prior to admission.

Time frame:
Patients not taking BZRs prior to admission

Results for this outcome have not been posted.

SecondaryRate (%) of Increased BZR Dose Prescription Among Patients Taking BZRs Prior to Admission

A dichotomous variable for an increased dose prescription among patients taking BZRs prior to admission.

Time frame:
Patients taking BZRs prior to admission

Results for this outcome have not been posted.

SecondaryRate (%) of Post-hospitalization Fall-related Injuries as Healthcare Utilization (Hospitalization, ED Visits, Urgent Care Visits, or Office Visits)

The investigators define post-hospitalization fall-related injuries as healthcare utilization (hospitalization, ED visits, urgent care visits, or office visits) due to fall-related injuries within 30 days of discharge of the index admission. The investigators will link Medicare claims data to trial data to track this outcome at the individual patient level.

Time frame:
Fall-related injuries within 30 days of discharge of the index admission

Results for this outcome have not been posted.

SecondaryRate of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Stratified by Patient Age Groups

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified by patient age groups. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Stratified According to Time Periods That Had Changes in the Intervention and Control Arms

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge stratified according to time periods that had changes in the intervention and control arms. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate of 30 Day Post Hospitalization in ED Visits (Same Hospital) Restricted to Medication-related Utilization

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge restricted to medication-related utilization. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

SecondaryRate of 7 Day Post-discharge Hospitalization Medication-related Post-discharge Utilization.

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 7 days of discharge by hospitalization medication-related post-discharge utilization. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 7 days of discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30-day Post-discharge Hospital Utilization With ED Visits, Observation Stays, and Inpatient Readmissions Counted Separately (Including Hospitals at Least Statewide).

A patient is readmitted to a hospital under inpatient or observation status or has an ED visit within 30 days of discharge (including hospitals at least statewide). The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to a hospital or ED visit within 30 days of discharge (checking at least all same state facilities)

Results for this outcome have not been posted.

Secondary30-day, All-cause Mortality After Hospital Discharge

All-cause mortality rate and survival analysis through Day 30 after hospital discharge.

Time frame:
Death occurring within 30 days after hospital discharge

Results for this outcome have not been posted.

SecondaryRate (%) of 30 Day Post-discharge Hospitalizations and ED Visits (Same Hospital) Among Patients Who Were Enrolled and Received the Intervention, Compared to Patients Who Were Eligible Yet Not Enrolled During the Study Period.

A patient is readmitted to the same hospital (including observation stays) or has an ED visit within 30 days of discharge. The investigators will exclude foreseen readmissions, which include: transplants, chemotherapy or radiotherapy, treatment follow-up, rehabilitation care, and planned operations.

Time frame:
Hospitalization to the same hospital or ED visit within 30 days of discharge

Results for this outcome have not been posted.

Adverse events

Collected over From the time of randomization (near hospital admission) up to 90 days after hospital discharge. Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Pharmacist Arm330/3,239 (10.2%)1,485/3,239 (45.8%)0/3,239 (0%)
Usual Care334/3,239 (10.3%)1,438/3,239 (44.4%)0/3,239 (0%)
Most frequent serious events
Most frequent serious events
EventPharmacist ArmUsual Care
90-day post-discharge utilizationGeneral disorders1155/32391104/3239
30-day post-discharge utilization (same hospital)General disorders662/3239666/3239

Baseline characteristics

Age, Continuous
Age, Continuous(years)Pharmacist ArmUsual CareTotal
Mean75.5 ± 10.275.6 ± 10.275.5 ± 10.2
Sex: Female, Male
Sex: Female, Male(Participants)Pharmacist ArmUsual CareTotal
Female158615773163
Male162716383265
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Pharmacist ArmUsual CareTotal
American Indian or Alaska Native6814
Asian139118257
Native Hawaiian or Other Pacific Islander000
Black or African American479475954
White230323674670
More than one race000
Unknown or Not Reported286247533
Study Site
Study Site(Participants)Pharmacist ArmUsual CareTotal
Cedars-Sinai Medical Center129913002599
Brigham and Women's Hospital191419153829
08

Study locations

2 sites
  • Cedars-Sinai Medical Center
    Los Angeles, California 90048, United States
  • Brigham and Women's Hospital
    Boston, Massachusetts 02115, United States
09

References and documents

Publications

  • Pevnick JM, Kennelty K, Nguyen AT, Amer K, Berdahl CT, Cook-Wiens G, Fanikos J, Fiskio J, Gotanda H, Guan J, Henreid AJ, Keller MS, Ko EM, Leang DW, Malkhasian Y, Matta L, Moriarty D, Murry L, Muske A, Nuckols TK, Oche O, Ortiz AS, Phung E, Qureshi N, Shane R, Wu S, Schnipper JL; PHARM-DC Group. Pharmacist-Led Discharge Care to Reduce Postdischarge Health Care Utilization: A Randomized Clinical Trial. JAMA Netw Open. 2026 Mar 2;9(3):e260719. doi: 10.1001/jamanetworkopen.2026.0719. PubMed 41842899 ↗
  • Murry LT, Keller MS, Pevnick JM, Schnipper JL, Kennelty KA; PHARM-DC Group. A qualitative dual-site analysis of the pharmacist discharge care (PHARM-DC) intervention using the CFIR framework. BMC Health Serv Res. 2022 Feb 12;22(1):186. doi: 10.1186/s12913-022-07583-5. PubMed 35151310 ↗
  • Pevnick JM, Keller MS, Kennelty KA, Nuckols TK, Ko EM, Amer K, Anderson L, Armbruster C, Conti N, Fanikos J, Guan J, Knight E, Leang DW, Llamas-Sandoval R, Matta L, Moriarty D, Murry LT, Muske AM, Nguyen AT, Phung E, Rosen O, Rosen SL, Salandanan A, Shane R, Schnipper JL. The Pharmacist Discharge Care (PHARM-DC) study: A multicenter RCT of pharmacist-directed transitional care to reduce post-hospitalization utilization. Contemp Clin Trials. 2021 Jul;106:106419. doi: 10.1016/j.cct.2021.106419. Epub 2021 Apr 28. PubMed 33932574 ↗

Study documents

  • Protocol and statistical analysis plan · Aug 25, 2023

Documents are hosted by the registry — open the source record to download them.

Individual participant data

Plan to share: No

10

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT04071951
Lead sponsor
Cedars-Sinai Medical Center
Collaborators
National Institute on Aging (NIA)
Responsible party
Josh Pevnick (Associate Professor of Medicine, Cedars-Sinai Medical Center) — Principal investigator
First posted
Aug 28, 2019
Start date
Dec 23, 2019
Primary completion
Aug 28, 2024
Completion
Jan 2027 (estimated)
Results posted
Oct 29, 2024
Last update
Apr 2, 2026

Study contacts

Joshua Pevnick
principal investigator · Associate Professor of Medicine

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

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