Feasibility Randomised Controlled Trial Exploring Implementation of the Compassionate Mindful rEsilience pRogram for People With pUlmonaRY Fibrosis: The MERcURY Study
MERcURY
2 other identifiers
interventional
21
1 country
1
Brief Summary
Pulmonary fibrosis (PF) is a chronic lung condition in which scar tissue gradually forms, impairing oxygen transfer and causing breathlessness. Individuals with PF frequently experience anxiety and depression, yet supportive care remains underdeveloped, and few evidence-based psychological interventions exist for this population, representing a critical gap in care. This feasibility randomised controlled trial (RCT) evaluated the Compassionate Mindful Resilience (CMR) programme, a 4-week online, nurse-led mindfulness-based intervention designed to improve psychological outcomes in people living with PF.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Dec 2024
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 21, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 18, 2025
CompletedFirst Submitted
Initial submission to the registry
August 12, 2026
CompletedFirst Posted
Study publicly available on registry
August 24, 2026
CompletedAugust 24, 2026
March 1, 2026
5 months
August 12, 2026
August 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Feasibility of the intervention
Adherence
From enrollment until the follow up interview was completed (up to 10 weeks)
Secondary Outcomes (1)
The feasibility of collecting data on anxiety, depression, well-being, mindfulness, resilience, and self-compassion
Baseline (week 1), post-CMR (week 4), and four-week follow-up (week 8)
Other Outcomes (1)
Feasibility of recruitment and retention
From recruitment until the end of the study (up to 5 months)
Study Arms (2)
Intervention group
EXPERIMENTALCMR is an internationally accredited 4-week programme with 2-hour online sessions delivered via Microsoft Teams
Waitlist group
NO INTERVENTIONThis group did not receive the CMR intervention until all intervention groups had completed CMR.
Interventions
It is an internationally accredited 4-week programme with 2-hour online sessions delivered via Microsoft Teams
Eligibility Criteria
You may qualify if:
- have a confirmed diagnosis of PF
- be aged 18 years or older
- reside in the UK or Ireland
- have the capacity to provide informed consent
- demonstrate a commitment to attend all four CMR sessions (demonstrated through discussion with the mindfulness teacher during screening)
- have access to an internet-enabled device.
You may not qualify if:
- No diagnosis of PF
- under 18 years old
- live outside of UK or Ireland
- no capacity to provide informed consent
- not willing to attend all four CMR sessions
- no access to an internet-enabled device.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Queen's University Belfast
Belfast, Please Select, BT7 1NN, United Kingdom
Related Publications (2)
Mc Veigh C, Reid J, Larkin P, Porter S, Hudson P. Palliative care for people with non-malignant respiratory disease and their carers: a review of the current evidence. J Res Nurs. 2019 Sep;24(6):420-430. doi: 10.1177/1744987119840066. Epub 2019 Apr 29.
PMID: 34394556BACKGROUNDMc Veigh C, Reid J, Larkin P, Porter S, Hudson P. The experience of palliative care service provision for people with non-malignant respiratory disease and their family carers: An all-Ireland qualitative study. J Adv Nurs. 2018 Feb;74(2):383-394. doi: 10.1111/jan.13453. Epub 2017 Nov 27.
PMID: 28910509BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Dr
Study Record Dates
First Submitted
August 12, 2026
First Posted
August 24, 2026
Study Start
December 1, 2024
Primary Completion
April 21, 2025
Study Completion
July 18, 2025
Last Updated
August 24, 2026
Record last verified: 2026-03
Data Sharing
- IPD Sharing
- Will not share