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PalliDrone - Scientific evaluation of the effectiveness and added value of drone-based medication delivery in palliative care

PalliDrone - Scientific evaluation of the effectiveness and added value of drone-based medication delivery in palliative care - PalliDrone

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00033811
Enrollment
50
Registered
2024-06-03
Start date
2024-04-24
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Z51.5

Interventions

Group 1: Employees of the hospice and SAPV (care professionals) Caring relatives of palliative care patients palliative care patients palliative care physicians T0 Needs analysis April - July 2024: C

Sponsors

AG Versorgungsforschung / Pflege im Krankenhaus, Department für Innere Medizin, Universitätsmedizin Halle, Medizinische Fakultät, Martin-Luther-Universität Halle-Wittenberg
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Palliative care patients in inpatient and outpatient care who are cared for by their family members or SAPV staff are included. Further criteria for inclusion are a minimum age of 18 years and sufficient written and spoken German language skills. In addition, it is stipulated that at least two deliveries per included patient must be made by courier or drone. Patients who are unable to give consent are also included.

Exclusion criteria

Exclusion criteria: No explicit exclusion criteria are defined. Exclusion occurs if the inclusion criteria do not apply.

Design outcomes

Primary

MeasureTime frame
WAZ1: Reduction in time to delivery through drone-based medication delivery compared to conventional delivery by courier service The courier service uses the "Vimcar" service to determine the delivery time. The delivery time of the drone is technically recorded by the drone operator. The delivery time is measured from the time the medication is ordered (triggering the process within the app for drone-based delivery or by email/fax/phone for the courier service) at the pharmacy until the medication is accepted by the caring relatives of palliative care patients or responsible SAPV service. Processes that include orders from wholesalers are excluded from the delivery time. The delivery time for each delivery for each patient is recorded at three measurement times: Study inclusion (baseline), after two successful deliveries and after three successful deliveries. WAZ2: Difference in quality of life / satisfaction of family caregivers between a drone-based medication delivery and a courier service delivery The differences in quality of life/satisfaction of caring relatives are assessed with the QOLLTI-F v2 and FAMCARE-6 at 3 measurement points: study inclusion (baseline), after 2 successful deliveries and after three successful deliveries. WAZ3: Feeling of time relief through a drone-based medication delivery by nursing staff and caregiving relatives compared to the courier service Three additional scaling questions on the intensity of the burden and two further free-text questions on the reasons for the burden and possible resources were added to the FAMCARE-6 in order to determine the time relief of caring relatives and nursing staff. The questionnaire is collected at three measurement points: study inclusion (baseline), after two successful deliveries and after three successful deliveries. In addition to these measures, a core data set recommended by the DGP and DHPV is also collected within the PalliDoc software used by the SAPV services and completed by the SA

Secondary

MeasureTime frame
WAZ4: Difference of acceptance (perceived usability) between conventional courier service and the drone-based medication system User acceptance is assessed using the System Usability Scale (SUS) at three measurement points: study inclusion (baseline), after two successful deliveries and after 3 successful deliveries. The SUS can be used to determine the perceived usability of conventional medication ordering by telephone/fax or e-mail (pre-phase) and the app and drone (post-phase).

Countries

Germany

Contacts

Public ContactFranziska Fink

AG Versorgungsforschung / Pflege im Krankenhaus, Department für Innere Medizin, Universitätsmedizin Halle, Medizinische Fakultät, Martin-Luther-Universität Halle-Wittenberg

franziska.fink@uk-halle.de+49 345 557 5483

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026