RandomisED Control Trial to Understand Whether Prescribing Choice for inhalErs is Influenced by Knowledge of the CARBON Footprint (REDUCE Carbon)
REDUCE- Carbon
3 other identifiers
interventional
3,782
1 country
1
Brief Summary
Climate change is a huge and present threat, with the devastating effects being increasingly seen in everyday life. The NHS contributes substantially to the UKs carbon footprint with an estimated 23 million tonnes gCO2Eq per year, 3% of which comes from pMDIs. There are a number of alternative inhalers, such as DPIs, which do not use propellant and therefore have a significantly lower carbon footprint. There is a call to move towards greener inhalers as part of the NHS long term plan for sustainability, to reduce the carbon footprint and therefore the environmental impact and help protect the health of our patients today and in the future. When recommending an inhaler, a number of factors are usually considered including the ability of the patient to use the device and its cost. Up until now the environmental impact of each inhaler is not routinely available and therefore is not normally considered in prescription choice. Given the increasing evidence supporting the sizeable impact that pMDIs are having on global warming, there needs to be a shift in practice where the climate impact forms part of the decision-making process. This study is looking to explore prescribing behaviours surrounding inhaler selection and in particular whether knowledge of the carbon footprint of inhalers has any sway on prescribing preference. By better understanding the decision-making process, this will allow the production of more comprehensive asthma management guidelines and potentially facilitate a drive to greener inhaler prescribing practices.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable asthma
Started Mar 2022
Typical duration for not_applicable asthma
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 28, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
August 28, 2025
CompletedFirst Submitted
Initial submission to the registry
August 19, 2026
CompletedFirst Posted
Study publicly available on registry
September 17, 2026
CompletedSeptember 17, 2026
September 1, 2026
3.5 years
August 19, 2026
September 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Health Care Practitioner Preference
The number and proportion of HCPs preferring high or low carbon inhalers between carbon-containing and non-carbon-containing groups, for each case separately and across all cases in total.
At completion of the online questionnaire (approximately 10 minutes)
Secondary Outcomes (4)
Rank Order of Preference
At completion of the online questionnaire (approximately 10 minutes)
Inhaler Recycling Recommendation
At completion of the online questionnaire (approximately 10 minutes)
Inhaler Recycling Facilities
At completion of the online questionnaire (approximately 10 minutes)
Use of Wessex Asthma Network Guidelines
At completion of the online questionnaire (approximately 10 minutes)
Study Arms (2)
Control Arm
OTHERParticipants receive the current standard Wessex Asthma Network inhaler guidelines with no information regarding the carbon footprint of individual inhalers
Intervention Arm
OTHERParticipants receive the Wessex Asthma Network inhaler guidelines plus information containing the carbon footprint for individual inhalers.
Interventions
Wessex Asthma Network inhaler guidelines plus the carbon footprint infromation for individual inhalers.
current standard Wessex Asthma Network inhaler guidelines with no information regarding the carbon footprint of individual inhalers
Eligibility Criteria
You may qualify if:
- Aged ≥18 years
- Working as an HCP within the NHS in a primary or secondary care setting
- Able to provide written e-consent
- Able to understand and complete the clinical case scenarios
You may not qualify if:
- Inability to understand or comply with study procedures and/or inability to give fully informed consent.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Portsmouth Hospitals University NHS Trust, Research Department
Portsmouth, Hampshire, PO63LY, United Kingdom
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Professor Thomas Brown
Portsmouth Hospitals NHS Trust
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 19, 2026
First Posted
September 17, 2026
Study Start
March 1, 2022
Primary Completion
August 28, 2025
Study Completion
August 28, 2025
Last Updated
September 17, 2026
Record last verified: 2026-09
Data Sharing
- IPD Sharing
- Will not share