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A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)

A Pharmacist-Led Intervention to Increase Inhaler Access and Reduce Hospital Readmissions (PILLAR)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03927820
Acronym
PILLAR
Enrollment
914
Registered
2019-04-25
Start date
2019-09-09
Completion date
2026-06-01
Last updated
2026-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma, COPD

Keywords

inhaler, pharmacy

Brief summary

The goal of this study is to assess the impact of pharmacist-led benefits investigations and application of clinical practice guidelines on patient access to inhalers and time to hospital readmission or Emergency Department (ED) visit.

Interventions

OTHERBenefits investigation

The study pharmacist will review the prescribed inhaler for 1) insurance coverage and 2) clinical appropriateness. The pharmacist will conduct a benefits investigation at time of hospital admission. The benefits investigation involves running test claims for inhalers to determine the most cost-effective inhaler for the patient's insurance plan. The study pharmacist will utilize clinical practice guidelines to assess appropriateness of the prescribed inhaler. Based on this review, the study pharmacist will submit a pharmacy consult to the inpatient pharmacist on the patient's healthcare team who will pend the inhaler orders (changing the patient's prescribed inhaler, if necessary) for the prescriber to send to the Meds to Beds discharge pharmacy. The Meds to Beds pharmacist will counsel the patient on inhaler use techniques prior to discharge.

Sponsors

Vanderbilt University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult patient admitted to Vanderbilt University Medical Center (VUMC) (excluding surgery services) * on a long acting inhaler or prescribed a long acting inhaler during admission.

Exclusion criteria

* Diagnosis of cystic fibrosis * Diagnosis of graft versus host disease (GVHD) * no medication insurance * discharge to any post-acute care facility or inpatient hospice * death during hospitalization

Design outcomes

Primary

MeasureTime frameDescription
Time to either hospital readmission or ER visit6 monthsCombined time (days) to either hospital readmission or emergency department visit after hospitalization (all outcomes measured at 6 months post-discharge with a 3 month interim analysis)

Secondary

MeasureTime frameDescription
Frequency of ED visit6 monthsnumber of ED visits 6 months post-discharge
frequency of hospital readmissions6 monthsnumber of hospital readmission 6 months post-discharge
time to 1st ED visit (days)6 monthstime until the first ED visit post-discharge
time to 1st readmission (days)6 monthstime until the first readmission post-discharge
frequency of prescribed inhaler at discharge6 monthsnumber of times the recommended inhaler was prescribed at discharge
frequency of short course prescription of oral steroid6 monthsnumber of oral steroid prescriptions in the 6 months post-discharge

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORKristina Niehoff, PharmD

Vanderbilt University Medical Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 28, 2026