CClinicalTrials.gg
CompletedNCT02336490Updated Oct 30, 2015

Randomized Pilot Trial of the Impact of Bedside Delivery of Discharge Medications to Pediatric Patients With Asthma

An interventional study of Discharge Medication Delivery Service in Asthma, sponsored by Boston Medical Center. Completed at 1 site in United States. Open to participants aged 2 Years to 17 Years. Per ClinicalTrials.gov, last updated 2015-10-30.

Sponsored by Boston Medical Center · Not applicable, Interventional, and Health services research

Phase
Not applicable
Study type
Interventional
Enrollment
23
Allocation
Randomized
Ages
2 Years to 17 Years
Sex
All
01

Study summary

This randomized pilot study proposes to field-test key logistical aspects of studying an intervention already available to patients on the pediatric ward, namely a discharge medication delivery service, called "Meds-in-Hand," which has been refined via a quality improvement process, but not rigorously studied nor fully implemented.

Read the detailed description

At this time, Meds-in-Hand is not currently utilized for approximately 40% of patients admitted to the pediatric ward at Boston Medical Center. Currently patients do not receive their discharge medications via the delivery service for a variety of reasons, however they continue to receive the usual care standard employed by most hospitals, where prescriptions are sent to their home pharmacy for pickup after discharge. This study does not change the actual medications patients receive, but how and when they get them. Rigorous study of the relationship between Meds-in-Hand and patient satisfaction and clinical outcomes has not been performed to date, so there is equipoise about the value of the intervention, however observational data in the population in question, namely children admitted for an asthma exacerbation, suggest that patients who receive Meds-in-Hand prior to discharge have a reduced likelihood of a return visit to the Emergency Department in 30 days. The study will focus on parent-patient dyads admitted with an asthma exacerbation where the child is aged 2-17 years, however parents will be the exclusive study subjects. Parents of the patients will be asked a baseline, in-hospital survey as well as participate in phone follow-up interviews to report on the patient experience and parent-reported child health outcomes at approximately 3 and 30 days after leaving the hospital. 60 total parents will be enrolled, 30 in each arm of the study. This pilot study will also obtain empiric estimates of key study parameters to inform future study design and begin to examine trends between the groups of patients who are randomized to the Meds-in-Hand intervention and those randomized to usual care.

02

Conditions studied

  • Asthma

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03

In context

Asthma

3,921 studies on the registry are indexed under Asthma; 507 are open to participants now.

This study's enrollment of 23 is below the median of 83 across 2,752 interventional studies indexed under Asthma.

Browse Asthma studies →

Lead sponsor

Boston Medical Center is the lead sponsor of 314 studies on the registry; 34 are open to participants now.

Of its 34 completed or terminated interventional studies of FDA-regulated products, 28 (82%) have results posted.

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

04

Who can participate

Ages eligible
2 Years to 17 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • admission includes treatment for asthma exacerbation
  • discharge medications will require a new prescription
  • primary care taker speaks english or spanish

Exclusion criteria

Exclusion Criteria:

  • patients being discharge outside of the operating hours of the delivery service
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
23 participants (actual)

Study arms

  • No intervention
    Usual Care

    discharge medication prescriptions are printed or sent electronically to a patient's pharmacy of choice

  • Active comparator
    Meds-in-Hand

    discharge medication delivery service: discharge prescriptions are filled at the hospital pharmacy and delivered to patients before they leave the hospital

    Other: Discharge Medication Delivery Service

Interventions

  • OtherDischarge Medication Delivery Service

    hospital-owned outpatient pharmacy fills and delivers discharge medications to patients in their rooms prior to discharge

06

What researchers measure

Primary outcomes

  1. Patient Experience measured by phone call followup interview

    phone call followup interview to assess the patient experience

    Time frame: 30 days

07

Study locations

1 site
  • Boston Medical Center
    Boston, Massachusetts 02118, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 30, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02336490
Lead sponsor
Boston Medical Center
Responsible party
Jonathan Hatoun (General Academic Pediatric Fellow, Boston Medical Center) — Principal investigator
First posted
Jan 13, 2015
Start date
Jan 2015
Primary completion
May 2015
Completion
Jul 2015
Last update
Oct 30, 2015

Study contacts

Jonathan Hatoun, MD, MPH
principal investigator · Boston Medical Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2015. You cannot join it, but the record below documents what was studied.

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