- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04990843
E-Drone: Transforming the Energy Demand of Supply Chains Through Integrated UAV-to-land Logistics for 2030 (E-Drone)
Vans are the fastest-growing category of licensed road vehicle in the UK with growing carbon dioxide (CO2) emissions. The proposed research into how Unmanned Aerial Vehicles (UAVs) and land logistics systems can be combined and managed will provide fundamental new understanding into the impacts of regulation and operating criteria on energy efficiency and costs. Medical logistics could be the first domain to utilise UAVs on a commercial scale, with preliminary analysis on pathology logistics within Southampton indicating that UAVs would significantly reduce CO2 emissions. With the National Health Service (NHS) spending an estimated £2.5 billion annually on pathology logistics and with patient numbers rising, there is a need to re-think how logistics costs could be reduced whilst improving bleed-to-diagnosis times for patients and energy demand.
The research vision is to examine the energy reduction potential of logistics solutions involving UAVs operating alongside sustainable last-mile delivery solutions (cargo cycles and walking porters via micro-consolidation points).
This involves understanding UAV operations in airspace shared with manned aircraft. The project focuses on a case study and trials based around NHS pathology sample transportation in the Solent and Dorset region. The key research objectives are to:
- Investigate the collective transport and energy impacts of current 'business-as-usual' NHS pathology logistics across the Solent region;
- Develop new simulation tools to quantify the energy consumption of UAVs and land logistics systems resulting from new types of traffic regulation for shared airspace and the operating requirements of UAVs;
- Evaluate the impact on air space and energy use of a large scale take-up of UAVs for medical logistics across the Solent region;
- Understand stakeholder concerns about UAVs;
- Understand the regulatory and governance needs associated with UAV interventions that will lead to energy benefits in logistics.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Janet Dickinson, Professor
- Phone Number: +441202965853
- Email: jdickinson@bournemouth.ac.uk
Study Contact Backup
- Name: Suzy Wignall
- Phone Number: +441202961200
- Email: swignall@bournemouth.ac.uk
Study Locations
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Dorset
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Dorchester, Dorset, United Kingdom, DT1 2JY
- Dorset County Hospital NHS Foundation Trust
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Poole, Dorset, United Kingdom, BH15 2JB
- University Hospitals Dorset NHS Foundation Trust
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Hampshire
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Portsmouth, Hampshire, United Kingdom, PO6 3LY
- Portsmouth Hospitals University National Health Service Trust
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Southampton, Hampshire, United Kingdom, SO16 6YD
- University Hospital Southampton Nhs Foundation Trust
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
- Task 1.1 - health staff/managers dealing with dispatch or receipt of patient diagnostics, bloods or pharmacy products at hospitals and GP surgeries, and transport staff..
- Task 1.2 qualitative - key stakeholder groups involved in the project including, NHS staff, will be via the project teams' commercial partners, and the general public.
- Task 1.2 quantitative - a representative sample of the UK population.
- Task 1.3 - logistics staff and health staff/managers dealing with dispatch or receipt of patient diagnostics, bloods or pharmacy products at hospitals and GP surgeries.
- Task 5.1 - key stakeholder groups involved in the project logistics providers, and a wider sample of the 144 organisations that responded to the Government consultation on the Future of Drones (January 2019).
- Tasks 5.2 - Two sub-samples from task 5.1.
- Task 6.2 - key stakeholders and members of the general public.
Description
Inclusion Criteria:
Work Package 1
- Task 1.1: key informants in appropriate job roles, with attention purposefully paid to gender and age balance of participants.
- Task 1.2: Interviews - a purposeful recruitment strategy will seek participants with a range of socio-demographic characteristics. Questionnaire - Prolific (or a similar commercial company) will distribute the questionnaire (n~1000) to achieve a representative sample of the UK population.
- Task 1.3: key informants in appropriate job roles, with attention purposefully paid to gender and age balance of participants.
Work Package 5
• Stakeholders with an interest in UAV use with a purposeful selection of participants with a range of socio-demographic characteristics.
- Work Package 6 • Anyone interacting with the serious game in dissemination events.
Exclusion Criteria:
• There are no specific exclusion criteria, though clearly some tasks require key informants with specific knowledge.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Questionnaire to a representative panel of the public
Time Frame: 1 - 33 months
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To explore representations of UAVs
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1 - 33 months
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Questionnaire to a representative panel of the public
Time Frame: 1 - 33 months
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To understand public concerns
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1 - 33 months
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Questionnaire to a representative panel of the public
Time Frame: 1 - 33 months
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To determine how UAVs empower or constrain pathways to adoption
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1 - 33 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Janet Dickinson, Professor, Professor in Tourism
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- RED 11731
- 295372 (Other Identifier: IRAS)
- EP/V002619/1 (Other Grant/Funding Number: The Engineering and Physical Sciences Research Council)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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