Die-logue Program for Community Dwelling Adults: A Randomized Controlled Trial
Effects of a Die-logue Program in Enhancing Community Dwelling Adults's Death Attitudes, Coping With Death and Readiness for Advance Care Planning: A Two-phase Study
2 other identifiers
interventional
148
1 country
1
Brief Summary
The goal of this clinical trial is to evaluate whether the Die-logue program can improve attitudes toward death, coping with death, and readiness for advance care planning (ACP) among community-dwelling middle-aged adults aged 40-60 years who have not completed any advance directives and not diagnosed with any life limiting diseases. This study aims to address the following research questions:
- Does the Die-logue program improve community-dwelling middle-aged adults' attitudes towards death, ability to cope with death, readiness and uptake for Advanced Care Planning (ACP).
- What are community-dwelling middle-aged adults' perceptions of advance care planning, death and dying, and their experiences of participation in the Die-logue program. Researchers will compare participants who receive the Die-logue program (death conversation and online ACP education) with participants who receive only the online ACP education to see if informal death conversations improve attitudes toward death, coping with death, and readiness for ACP. Participants will:
- Complete online questionnaires measuring attitudes toward death, coping with death, and readiness for advance care planning.
- Participate in a facilitator-led group discussion session about perceptions of death, coping with death, and readiness for ACP (intervention group only).
- Complete an asynchronous online ACP education session consisting of short recorded videos and an online discussion forum (both intervention and control group).
- Complete follow-up surveys, including a 6-month follow-up assessing whether they have undertaken advance care planning.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2026
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
April 1, 2026
CompletedFirst Submitted
Initial submission to the registry
April 6, 2026
CompletedFirst Posted
Study publicly available on registry
April 13, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2027
April 13, 2026
March 1, 2026
1.8 years
April 6, 2026
April 6, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
Death Attitudes
Death Attitude Profile Revised Scale (DAP-R)
Before intervention
Death Attitudes
Death Attitude Profile Revised Scale (DAP-R)
Immediately after intervention
Secondary Outcomes (8)
Coping with Death
Before intervention
Coping with Death
Immediately after intervention
Coping with Death
6 months after intervention
Death Attitudes
6 months after intervention
Readiness for Advance Care Planning
Before intervention
- +3 more secondary outcomes
Study Arms (2)
Intervention Group
EXPERIMENTALParticipants in this arm will receive the two-session Die-logue Program. Session 1 is an on site, facilitator-led group discussion lasting 2 hours, covering: 1. Perceptions of death and dying. 2. Coping with death. 3. Readiness for Advance Care Planning (ACP). Session 2 is an online asynchronous learning session with short videos on ACP with discussion forums.
Control Group
ACTIVE COMPARATORParticipants in this arm will only receive the online ACP education component, identical to Session 2 of the Die-logue programme. No facilitator-led group discussions are provided.
Interventions
On site, facilitator-led group discussion lasting 2 hours, covering: 1) Perceptions of death and dying. 2) Coping with death. 3) Readiness for Advance Care Planning (ACP)
An online asynchronous learning session with short videos on ACP with discussion forums.
Eligibility Criteria
You may qualify if:
- Between the ages of 40 to 60 years
- Able to comprehend the English language
- Have not completed any form of advance directives
- Able and willing to participate in the Die-logue programme and surveys
You may not qualify if:
- Individuals diagnosed with any life limiting diseases
- Individuals with self-reported history of mental health disorders or neurological disorders
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National University of Singapore
Singapore, Singapore
MeSH Terms
Conditions
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant Professor
Study Record Dates
First Submitted
April 6, 2026
First Posted
April 13, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
December 31, 2027
Study Completion (Estimated)
December 31, 2027
Last Updated
April 13, 2026
Record last verified: 2026-03