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Not yet recruitingNCT06040151PILLS@HOMEUpdated Sep 15, 2023

Evaluating Mobile-based Medication Reconciliation by Patients at Home

An observational study in Patients, sponsored by Erasmus Medical Center. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-09-15.

Sponsored by Erasmus Medical Center · Observational

From the registry’s dates

  • Primary completion was expected by Mar 2024, 2 years 7 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
39
Ages
18 Years and older
Sex
All
01

Study summary

Medication reconciliation (MR) is essential to limit drug-related problems that occur during care transitions in and out of care institutions. Pharmacy-led medication reconciliation has been shown to reduce medication discrepancies, preventable harm and hospital readmissions. However, these consultations are time-consuming. The Erasmus Medical Center is currently developing a mobile-based patient portal. After receiving an invitation to perform medication reconciliation in the app, patients can review their medication and allergies at home. Next, pharmacy technicians manually verify all patient-entered data on completeness and quality. The investigators hypothesize that mobile-based medication reconciliation results in increased patient insight. Yet, it is unknown if mobile-based medication reconciliation is feasible, saves time, and is of high quality.

Therefore, the primary study objectives are to assess (1) the feasibility of patients performing medication reconciliation using a mobile-based patient portal, (2) the time investment of pharmacy technicians in mobile-based medication reconciliation (and related costs), in comparison to standard practice, and (3) the quality of patients' pre-verified medication lists. The secondary study objective is to assess patients' and pharmacy technicians' acceptability of performing medication reconciliation using a mobile-based patient portal.

This is a prospective quality evaluation study assessing mobile-based medication reconciliation. All adult patients (18 years or older) who are admitted to (a selection of) clinical ward in Erasmus Medical Center and who are asked to complete medication reconciliation are eligible. In the patient app, patients review ('pre-verify') their medications and allergies, after which pharmacy technicians check and manually approve ('verify') all patient-entered data and determine whether a follow-up interview is needed.

Feasibility is defined as the successful completion rate of digital medication reconciliation, and the need for additional interviews. Time investment by pharmacy technicians (and related costs) are determined by timing the duration of all patient-bound medication reconciliation-related tasks, both in standard care and when using mobile-based reconciliation. The quality of verification is determined by comparing patients' pre-verified medication list to pharmacy technician-verified lists. Acceptability is defined as the perceived usability of medication reconciliation by patients and by pharmacy technicians.

02

Conditions studied

  • Patients

Keywords

  • Patients with all conditions are eligible
03

In context

Lead sponsor

Erasmus Medical Center is the lead sponsor of 466 studies on the registry; 179 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

All adult patients (18 years or older) who are asked to complete medication reconciliation before a planned admission to the clinical ward of selected pilot departments in Erasmus MC are eligible to participate in this study.

Inclusion criteria

  • 18 years or older
  • Planned admission to the clinical ward of participating pilot departments in Erasmus MC

Exclusion criteria

Exclusion Criteria:

  • No potential subject will be excluded from participation in this study.
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
39 participants (estimated)
Patient registry
No

Groups and cohorts

  • Users of mobile-based medication-reconciliation app

    Adult patients (18 years or older) who are asked to complete medication reconciliation before a planned admission to the clinical ward of selected pilot departments in Erasmus Medical Center

    Device: Digizorg mobile app (quality evaluation study)

Interventions

  • DeviceDigizorg mobile app (quality evaluation study)

    Erasmus Medical Center is developing a state-of-the-art, mobile-based patient portal that combines up-to-date medication lists from all healthcare providers involved in a patient's care. Other functionalities include: accessing health information, viewing and planning appointments, teleconsulting, sending messages, filling in questionnaires, reporting self-measurements, and reading background information on diseases, medication, and other interventions. The patient portal will primarily be implemented in Erasmus Medical Center, and is ultimately intended for every patient, regardless of underlying condition.

06

What researchers measure

Primary outcomes

  1. Feasibility (1/4): completion rate of digital MR by patients

    The fraction of all patients who were invited to participate that participated

    Time frame: During quality evaluation of the patient app, an average of 3 months

  2. Feasibility (2/4): the time it takes patients to perform digital MR (in minutes)

    To assess the ease-of-use of performing medication reconciliation in the patient app

    Time frame: During quality evaluation of the patient app, an average of 3 months

  3. Feasibility (3/4): the need for live, follow-up interviews after performing digital MR

    The fraction of all patients who were invited to participate in digital MR who needed a live interview

    Time frame: During quality evaluation of the patient app, an average of 3 months

  4. Feasibility (4/4): how often the helpdesk was contacted

    The fraction of all patients who were invited to participate in digital MR who contact the helpdesk

    Time frame: During quality evaluation of the patient app, an average of 3 months

  5. The time investment by pharmacy technicians per patient in the digital MR process, compared to the current situation (in minutes)

    The time investment by pharmacy technicians per patient in the new workflow vs. the current situation, in which all patients are invited for a live interview

    Time frame: Before launch of the patient app, during an average of 2 months, and during quality evaluation of the patient app, an average of 3 months

  6. The quality of a patient's pre-verified medication list, compared to the pharmacy technician's verified medication list

    The number of discrepancies between the patient-reported medication list and the pharmacy-verified medication list (the number of changes made by a pharmacy technician in the MR process)

    Time frame: During quality evaluation of the mobile-based medication reconciliation tool, an average of 3 months

Secondary outcomes

  1. Acceptability (1/2): defined as the perceived usability of mobile-based MR by patients, assessed using short in-app questionnaires (VAS 1-5)

    To assess to what extent digital medication reconciliation is accepted by patients

    Time frame: During quality evaluation of the mobile-based medication reconciliation tool, an average of 3 months

  2. Acceptability (2/2): defined as the perceived usability of mobile-based MR by patients and pharmacy technicians, assessed using short qualitative interviews with both patients and pharmacy technicians

    To assess to what extent digital medication reconciliation is accepted by patients and pharmacy technicians

    Time frame: During quality evaluation of the mobile-based medication reconciliation tool, an average of 3 months

07

Study locations

No study locations are listed for this record.

08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06040151
Lead sponsor
Erasmus Medical Center
Responsible party
Alan Abdulla (dr. Alan Abdulla, Principal Investigator, Erasmus Medical Center) — Principal investigator
First posted
Sep 15, 2023
Start date
Oct 2023 (estimated)
Primary completion
Mar 2024 (estimated)
Completion
May 2024 (estimated)
Last update
Sep 15, 2023

Study contacts

Martijn Brands, MD
Contact
m.r.brands@erasmusmc.nl
0031205665675

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.

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