NCT06728254

Brief Summary

Linked Care aims to help healthcare professionals (nurses, doctors, pharmacists) interact efficiently and safely with IT support to improve patient information flows. It focuses on the medication ordering process, which currently involves time-consuming steps like calling doctors and traveling to get prescriptions. The project targets nursing staff, doctors, pharmacists, and patients, with indirect benefits for hospitals, social welfare organizations, and insurance bodies. This study evaluates the Linked Care solution by addressing the research question: Does an electronic ordering system improve the efficiency and quality of the regular medication process?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
70

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

4 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 6, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

December 11, 2024

Completed
27 days until next milestone

Study Start

First participant enrolled

January 7, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 29, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 29, 2025

Completed
Last Updated

September 24, 2025

Status Verified

September 1, 2025

Enrollment Period

6 months

First QC Date

December 6, 2024

Last Update Submit

September 19, 2025

Conditions

Keywords

medication processnursingtelehealthhome caremedication order

Outcome Measures

Primary Outcomes (1)

  • Time spent on medication related processes

    Measure of time efficiency recorded on a project-specific 14-day medication log. / Minimum value: 0 \[minutes\], maximum value: N/A. Higher scores mean a worse outcome. / Analysis metric: difference test vs. control, test group trend analysis. / Method of aggregation: mean.

    Baseline, 3-month follow-up, 6-month follow-up

Secondary Outcomes (4)

  • Overall score from the "Survey on psychological stress in mobile care (BGW miab)

    Baseline, 3-month follow-up, 6-month follow-up

  • Overall score from a "Project-specific questionnaire on care-process quality".

    Baseline, 3-month follow-up, 6-month follow-up

  • Overall score from the "Usefulness, Satisfaction, and Ease of Use (PSSUQ) Questionnaire"

    3-month follow-up, 6-month follow-up

  • Overall score from the "Unified Theory of Acceptance and Use of Technology 2 (UTAUT2) Questionnaire"

    3-month follow-up, 6-month follow-up

Other Outcomes (5)

  • Sample Characteristic Affiliation

    Baseline

  • Sample Characteristic Profession

    Baseline

  • Sample Characteristic Age

    Baseline

  • +2 more other outcomes

Study Arms (2)

Intervention (using Linked Care system)

EXPERIMENTAL

All nurses and caregivers participating in the intervention group use the newly installed mynevaToGo app to reorder medication. Nurses and nursing assistant level 2 also use the myneva Care Center software to keep the medication list prescribed by the GP. The solution is installed in advance on the duty cell phones by the IT department of the relevant care organization. Participating nurses and caregivers in the intervention group are instructed to handle the medication ordering process electronically (i.e., medication orders will be sent to the GPs via the Linked Care platform).

Device: medication management

Control

ACTIVE COMPARATOR

Care professionals in the convenience sampled control group continue to handle the usual medication process.

Other: Usual Care Group

Interventions

The test system consists of: * Linked care platform (backend) which provides a new possibility of data exchange for IT systems of caregivers, pharmacies, and GPs * User interfaces for caregivers as well as for the systems myneva.carecenter and mynevaTOgo * An extension of the user interface for GPs in their IT system (in the test only for the physician software PCPO by CompoGroup Medical ) * An extension of the user interface for pharmacists in their IT system (in the test only for pharmacies with software from Apothekerverlag) Functionally, the solution should, coordinate the medication requirements between pharmacies, GPs, and caregivers (subarea medication).

Intervention (using Linked Care system)

Usual care.

Control

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Actively pursuing at least one of the following health professions extramurally: nurse, nursing assistant level 1 or level 2 , elderly specialist caregiver, home care assistant
  • Active maintenance of nursing documentation and use of the duty cell phone
  • Age 18+ years
  • Willing to comply with all study-related procedures and provide informed consent

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (4)

Volkshilfe Gesundheits- und Soziale Dienste GmbH

Linz, 4200, Austria

Location

Wiener Rotes Kreuz- Rettungs-, Krankentransport-, Pflege- und Betreuungsgesellschaft m.b.H.

Vienna, 1030, Austria

Location

Johanniter Österreich Ausbildung und Forschung gem. GmbH

Vienna, 1210, Austria

Location

Volkshilfe Wien gemeinnützige Betriebs-GmbH

Vienna, Austria

Location

Related Publications (2)

  • Helmcke Stefan, Biesdorf Stefan, Bauer Florian, Berger Wernhard (2021). mckinseystudiedigitalisierung im gesundheitswesen die 47mrdeurochance fur Österreich.

    BACKGROUND
  • BGW miab für die Pflege und den stationären Wohnbereich der Behindertenhilfe Erstveröffentlichung 2002, Stand 01/2013 Hrsg. Berufsgenossenschaft für Gesundheitsdienst und Wohlfahrtspflege (BGW). Hamburg, Online: www.bgw-online.de

    BACKGROUND

Study Officials

  • Elisabeth Haslinger-Baumann, FH-Prof. Dr.

    FH Campus Wien University of Apllied Sciences

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Model Details: Non-randomized controlled trial, with participants unequally allocated to test and control groups (factor 5) in clusters
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Head of Research Center

Study Record Dates

First Submitted

December 6, 2024

First Posted

December 11, 2024

Study Start

January 7, 2025

Primary Completion

June 29, 2025

Study Completion

June 29, 2025

Last Updated

September 24, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Because the trial deals with sensitive health-related data, neither person-identifiable nor coded raw data will be made publicly available or shared upon request from other researchers.

Locations