CClinicalTrials.gg
Not yet recruitingNCT06793631Updated Jan 30, 2025

Mapping Financial Support for the Terminally Ill

An observational study in People with Terminal Illness, sponsored by University College, London. Not yet recruiting at 2 sites in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-01-30.

Sponsored by University College, London · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
40
Ages
18 Years and older
Sex
All
01

Study summary

People living with terminal illness (an illness that is not curable and likely to lead to death) are often unable to work and experience increased costs associated with their health, such as caring costs, needing to purchase aids for daily living (e.g., grab rails) and more travel for appointments. Family members frequently reduce the number of hours they work, or stop working all together, to care for their loved one. These factors exacerbate their risk of financial insecurity.

Health and social care professionals are frequently required to complete applications on behalf of patients and their families for these grants or schemes. It is difficult and time-consuming to identify suitable sources of financial support for families living with a terminal illness. There is little known about the families who are applying for this support, how often they need to use these services and why. Mapping these resources and understanding the experiences of those applying for this support will help to identify groups who are at risk of financial insecurity, speed up the application process, and provide understanding to inform future policies to reduce the risk of dying in poverty.

In the first phase of this study, the investigators conducted a mapping exercise, across England and Wales, to identify what voluntary and local government sources of support are available for people who are living with a terminal illness to apply for. In the second phase, the investigators want to identify potential barriers and facilitators to accessing this support through qualitative interviews with people who can refer to these sources of funding (e.g., social workers), the services (e.g., grant managers), and people who are living with a terminal illness and have applied for financial support.

Overall, this research will scope what financial support services are currently available that people living with terminal illness, and their families, are eligible to apply for across England and Wales, and importantly, what the key barriers and facilitators are to accessing these services.

Read the detailed description

This is the first study to explore this area and will scope what support exists and where gaps are, in terms of provision specifically for people with terminal illness. The investigators will also explore barriers and facilitators to providing and accessing financial support at different levels (individual, community, organisational, structural). This research will produce a point-in-time map of financial support services and a report of recommendations for how policy makers in England and Wales can address barriers and gaps in service provision. The focus will be on England and Wales as Scotland and Northern Ireland have devolved policies and infrastructure for provision of financial support, but our recommendations may have implications for these nations.

Aim(s): The overall aim of this research is to understand the availability, suitability, and accessibility of voluntary sector and local government financial support schemes for people living with terminal illness, and their families, in England and Wales. This will be achieved through the following objectives, completed in two phases.

Phase 1: Quantitative survey Objective 1. Mapping financial support services provided by voluntary organisations and local government that people with a terminal illness (and their families) are eligible to apply for across England and Wales.

Objective 2. Comparing availability of, and access to, financial support for different population groups and by geographical areas, including regions with differing deprivation profiles.

Phase 2: Qualitative interviews Objective 3. Understanding the experiences and perceptions of financial support from the perspective of a person living with terminal illness and their family, the referrer, and those providing financial support.

Ethical approval has been granted through University ethics for objectives 1 and 2 (phase 1) of this research (UCL REC reference 26921.001), on the 19th of February 2024).

02

Conditions studied

  • People with Terminal Illness

Keywords

  • terminal illness
  • financial insecurity
  • mapping analysis
  • living costs
03

In context

Lead sponsor

University College, London is the lead sponsor of 632 studies on the registry; 145 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants will be recruited across England and Wales.

Eligibility criteria

There are three participants groups for this research. For each group, there will be separate eligibility criteria. These groups are:

  1. Patient group: people with terminal illness (and/or their families/bereaved families) who have received financial support.
  2. Referral group: healthcare professionals who refer individuals for financial support (i.e., social workers, clinicians),
  3. Services group: people who work for a financial support service.

Patient group:

  1. Have a diagnosis of terminal illness by their healthcare provider, defined as someone with an advanced incurable illness (in case of bereaved families, having caring responsibility for someone with a terminal illness).
  2. Be over 18 years of age.
  3. Have capacity to participate. As people with terminal illness may also have comorbid conditions potentially affecting cognition (e.g. cancer and dementia), we will monitor capacity during their involvement in the qualitative interviews.
  4. Understand spoken English or Welsh to participate in an interview.
  5. Only bereaved families who had their loved one who had died in the previous 4 to 10 months will be recruited. This is to reduce the risk of experiencing any emotional distress linked to the topic discussed during the qualitative interviews. This timeline has found to be the optimal time for such work, whereby the carer feels ready to think about their loss but still has sufficient recall of events.

Referral group:

  1. They are a registered healthcare professional who have discussed financial support with people living with terminal illness.

Service group:

  1. They work for a group (either a charity or local authority) who provide financial support for the public.

Exclusion Criteria:

If any of the inclusion criteria are not met, the individual will be excluded. Participants with no capacity or if the researcher has concerns about their capacity to consent, will not be able to take part in the study. Bereaved families who had lost their loved ones very recently (within the previous 3 months) will be excluded.

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • People with terminal illness and/or their families/bereaved families.

    20 People with terminal illness (and/or their families/bereaved families) who have received financial support, and or have experience of applying for financial support/advice.

    Other: Participants will be interviewed qualitatively about experience of providing/receiving financial support for living costs

  • Referrers of financial support services for living costs

    10 Referrers (i.e., social workers, doctors, admiral nurses, nurses)

    Other: Participants will be interviewed qualitatively about experience of providing/receiving financial support for living costs

  • Financial support service workers

    10 Financial support service workers

    Other: Participants will be interviewed qualitatively about experience of providing/receiving financial support for living costs

Interventions

  • OtherParticipants will be interviewed qualitatively about experience of providing/receiving financial support for living costs

    There is no intervention for participants. Participants will receive qualitative interviews to explore their experience of financial insecurity

06

What researchers measure

Primary outcomes

  1. Financial insecurity

    We will deliver semi-structured qualitative interviews with people with terminal illness (and/or their families/bereaved families) to explore the experience of financial insecurity for those who may have had problems with living costs crisis. We will also interview referrers and service provider workers to explore their experience of providing financial support/advice for someone with terminal illness.

    Time frame: Day 1

07

Study locations

2 sites
  • Cardiff University
    Cardiff, United Kingdom
  • Marie Curie Palliative Care Research Department, Division of Psychiatry, University College London
    London, United Kingdom
08

References and documents

Individual participant data

Plan to share: Yes — Metadata will consist of: interview transcripts, study notes (researcher reflexive notes) and this will be (once anonymised) stored in an open UCL repository. Data will be anonymised once the data collection has ended, and the analysis has been completed. The data will be stored for a period of twenty years, following UCL guidelines. UCL and each participating site recognise that there is an obligation to archive study-related documents at the end of the study (as such end is defined within this protocol). The Chief Investigator confirms that he/she will archive the study master file at UCL for the period stipulated in the protocol and in line with all relevant legal and statutory requirements. The Principal Investigator at each participating site agrees to archive his/her respective site's study documents in line with statutory requirements.

Supporting information: Study protocol

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06793631
Lead sponsor
University College, London
Collaborators
Cardiff University
Responsible party
Sponsor
First posted
Jan 27, 2025
Start date
Mar 2025 (estimated)
Primary completion
Dec 2025 (estimated)
Completion
Dec 2025 (estimated)
Last update
Jan 30, 2025

Study contacts

Nicola White, PhD
Contact
n.g.white@ucl.ac.uk
+44 (0) 2076799057
Alessandro Bosco, PhD
Contact
alessandro.bosco@ucl.ac.uk
Emily Harrop, PhD
principal investigator · Cardiff University
Nuriye Kupeli, PhD
study chair · University College, London

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jan 2025. You cannot join it, but the record below documents what was studied.

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