NCT07757178Recruiting
Lived Experience Narratives in Dementia
Improving the Quality of Life for People Living With Dementia and Carers: The Design and Development of a Dementia Specific Online Narrative-Based Intervention With a Feasibility Study
Source: ClinicalTrials.gov · Last updated 11 Aug 2026
Brief summary (registry, in English)
The Lived Experience Narratives in Dementia (LEND) research programme involves five work packages (WP). WP1 explores how people living with dementia use narratives and how narratives can impact them. Findings will support the development of LEND theory. WP 2-3 focus on developing the digital Online LEND Intervention, assessing its usability and acceptability, and conducting a feasibility study within NHS memory assessment and community services. Activities across the first three WPs include interviews, focus groups, user-testing sessions, engagement evaluation interviews, and a two-arm randomised feasibility trial using a range of outcome measures. Findings from this stage will inform refinement of the intervention and determine the feasibility of progressing to a future randomised controlled trial (RCT) of the Online LEND Intervention. WP4 is the Online LEND Intervention two-arm RCT. WP5 involves dissemination. The protocol for WP4 and 5 have not yet been developed and rely on results from WP1-3.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 28 Jul 2026
- Start date
- 17 Nov 2025
- Primary completion date
- 31 Mar 2029
- Lead sponsor
- University of Nottingham
- Diseases
- Alzheimer disease
- NCT number
- NCT07757178
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 17 Nov 2025 to the primary completion date, 31 Mar 2029
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- General Inclusion Criteria (apply across WP1-WP3)
- Adults aged 18+.
- Able to give informed consent and participate meaningfully in the required tasks.
- Adequate communication ability in the required study language
- General Exclusion Criteria (apply across WP1-3)
- Living in a hospital or healthcare institution at the time of the study.
- Refusal or inability to provide informed consent, or lack of capacity to consent.
- Inability to comprehend participant information or communicate meaningfully
Age in the registry: 18 years to 99 years · Sex: All · Accepts healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Mental Health & Clinical Neurosciences, Institute of Mental Health Coordinator of this site? Confirm its status | Nottingham | United Kingdom | Recruiting |
| Nottinghamshire Healthcare NHS Foundation , Highbury Hospital Coordinator of this site? Confirm its status | Nottingham | United Kingdom | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.