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Completed

NCT Number: NCT06728254

Information Systems Connectivity to Improve Medication Process

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?

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Volkshilfe Gesundheits- und Soziale Dienste GmbH, Linz, Austria

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About this study

Background and rationale:

Linked Care aims to provide access to information relevant to care and support beyond the boundaries of the various care settings and primarily supports caregivers in the acquisition and transfer of information. The development of essential standards (e.g., a myCare Info) and the involvement of all affected target groups make it possible to develop practical IT tools for standardized networking in mobile care and nursing. The result will be an integrated, affordable, easy-to-use and well-connected IT system for care and support. The portal can be operated via mobile devices, PC, or tablets.

The McKinsey study demonstrates the significant potential of digitalization in the Austrian healthcare sector. According to this study, there is a 4.7-billion-euro opportunity for Austria. Approximately 70% of the potential benefits of increased productivity accrue to service providers, such as physicians and hospitals. The remaining 30% can be attributed to other players in the system, particularly health insurers, who benefit from reduced service utilization and improved care. Key factors in achieving these benefits include the implementation of the Austrian electronic health record (ELGA) and e-prescribing, which enable efficiency gains of EUR 690 million. Digitization is also sought after by regulators, patients, payers, and service providers in the Austrian healthcare system for improved efficiency and quicker access to data.

Helmcke et al. (2021) identify the following areas with the greatest potential for savings and benefits in the Austrian healthcare system:

  • Online interactions, especially through teleconsultation.
  • Paperless data, emphasizing standardized patient records/exchange and electronic prescriptions.
  • Automated workflows, particularly the networking of mobile caregivers.
  • Decision support and transparency of outcomes, including performance dashboards.
  • Patient self-management, primarily through tools for managing chronic conditions like diabetes.
  • Patient self-service for electronic scheduling.

Objectives:

This project aims to enable documenting healthcare professionals (such as nurses, general practitioners (GPs), and pharmacists) to interact efficiently, safely, and conveniently, with optimal IT support, to improve (or make more efficient) the patient-related information flows. The specific use cases studied are the process of ordering and in particular reordering medication. A significant time-saving potential has been identified in the transfer of medication information. The ordering process usually begins with nurses calling a GP as soon as they notice that a client has run out of medication and needs to be re-supplied when preparing the prescribed medication. The nurse then usually travels distances (e.g. by car) to obtain a prescription from the GP and collect the medication from the pharmacy. To do this, they need the client's insurance card, which has to be collected separately. The project is therefore aimed at four target groups: i) nursing staff who carry out the documentation, ii) GPs, and iii) pharmacists and finally iv) patients who make use of the care. In addition to the target groups studied in this trial, indirect beneficiaries include healthcare providers such as hospitals, social welfare organizations, rehabilitation clinics, public insurance bodies, etc. who ensure effective and efficient care. The trial aims to evaluate the entire process of data recording and data exchange via the newly created interfaces between the systems involved in practical use.

The primary research question of this study is: Does an electronic ordering system improve the efficiency and quality of the regular medication process?

Secondary research questions are:

  • Does the digital ordering system receive end-user acceptance?
  • Which impacts on the health and care system are generated by the implementation of the digital ordering system? (evaluated qualitatively)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Caregivers:

  • 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

Treatment and study plan

medication management

Device

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).

Usual Care Group

Other

Usual care.

Primary outcomes

  1. Time spent on medication related processes

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

    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.

Secondary outcomes

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

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

    Self-reported indications on 6 subitems on a 5-point Likert pseudometric scale. / Minimum value: 1, maximum value: 5. Higher scores mean a worse outcome. / Analysis metric: Difference test vs. control & test group trend analysis. / Method of aggregation: mean score.

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

    Time frame: Baseline, 3-month follow-up, 6-month follow-up

    Self-reported indications on 21 subitems on a 5-point Likert pseudometric scale. / Minimum value: 1, maximum value: 5. Higher scores mean a worse outcome. / Analysis metric: Difference test vs. control & test group trend analysis. / Method of aggregation: weighted mean score.

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

    Time frame: 3-month follow-up, 6-month follow-up

    Self-reported indications on 16 subitems on a 7-point Likert pseudometric scale. / Minimum value: 1, maximum value: 7. Higher scores mean a worse outcome. / Analysis metric: Difference test vs. control & test group trend analysis. / Method of aggregation: mean score.

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

    Time frame: 3-month follow-up, 6-month follow-up

    Self-reported indications on a 7-point Likert pseudometric scale with subitems in 4 domains: i) performance expectancy, ii) effort expectancy, iii) social influence, and iv) facilitating conditions. / Minimum value: 1, maximum value: 7. Higher scores mean a worse outcome. / Analysis metric: Difference test vs. control & test group trend analysis. / Method of aggregation: mean score.

Other outcomes

  1. Sample Characteristic Affiliation

    Time frame: Baseline

    Affiliation to a care-providing organization (selection from 4 participating organizations GSD, VHW, WRK, JOHA). Scale: nominal.

  2. Sample Characteristic Profession

    Time frame: Baseline

    Profession (selection from 5 options: certified nurse, specialist nursing assistant, nursing assistant level 1 or level 2 , home care assistant. Scale: nominal.

  3. Sample Characteristic Age

    Time frame: Baseline

    Age (years). Scale: metric.

  4. Sample Characteristic Gender

    Time frame: Baseline

    Gender (selection from 3 options: male, female, divers). Scale: nominal.

  5. Sample Characteristic Employment Extent

    Time frame: Baseline

    Employment extent (weekly contractual hours). Scale: metric.

Sponsors and collaborators

Lead sponsor

Peter Putz

Other

Collaborators

  • Johanniter Österreich Ausbildung und Forschung gem. GmbH
  • Volkshilfe Gesundheits- und Soziale Dienste GmbH
  • Volkshilfe Wien gemeinnützige Betriebs-GmbH
  • Wiener Rotes Kreuz- Rettungs-, Krankentransport-, Pflege- und Betreuungsgesellschaft m.b.H.

Registry information

Official study title

Effects of Care Information Systems Connectivity on Medication Process Efficiency and Quality (Linked Care): Protocol for a Cluster Allocated Controlled Trial

Acronym: LinkedCare

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Dec 11, 2024
Registry last updated
Sep 24, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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