E-Drone: Transforming the Energy Demand of Supply Chains Through Integrated UAV-to-land Logistics for 2030 (E-Drone)

January 10, 2024 updated by: Bournemouth University

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:

  1. Investigate the collective transport and energy impacts of current 'business-as-usual' NHS pathology logistics across the Solent region;
  2. 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;
  3. Evaluate the impact on air space and energy use of a large scale take-up of UAVs for medical logistics across the Solent region;
  4. Understand stakeholder concerns about UAVs;
  5. Understand the regulatory and governance needs associated with UAV interventions that will lead to energy benefits in logistics.

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

24

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Dorset
      • Dorchester, Dorset, United Kingdom, DT1 2JY
        • Dorset County Hospital NHS Foundation Trust
      • Poole, Dorset, United Kingdom, BH15 2JB
        • University Hospitals Dorset NHS Foundation Trust
    • Hampshire
      • Portsmouth, Hampshire, United Kingdom, PO6 3LY
        • Portsmouth Hospitals University National Health Service Trust
      • Southampton, Hampshire, United Kingdom, SO16 6YD
        • University Hospital Southampton Nhs Foundation Trust

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 99 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
To explore representations of UAVs
1 - 33 months
Questionnaire to a representative panel of the public
Time Frame: 1 - 33 months
To understand public concerns
1 - 33 months
Questionnaire to a representative panel of the public
Time Frame: 1 - 33 months
To determine how UAVs empower or constrain pathways to adoption
1 - 33 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Janet Dickinson, Professor, Professor in Tourism

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2021

Primary Completion (Actual)

December 31, 2023

Study Completion (Actual)

December 31, 2023

Study Registration Dates

First Submitted

July 15, 2021

First Submitted That Met QC Criteria

July 26, 2021

First Posted (Actual)

August 5, 2021

Study Record Updates

Last Update Posted (Estimated)

January 11, 2024

Last Update Submitted That Met QC Criteria

January 10, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

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

No

Studies a U.S. FDA-regulated device product

No

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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