Pure Global AI
NCT06152120Enrolling by invitation

Preparing Surrogates of Dementia Patients Through an Advance Care Planning Intervention

Preparing Surrogates of Dementia Patients for In-the-moment Decision Making Through a Structured Advance Care Planning Intervention: A Mixed-methods Pilot Study
The University of Hong KongClinicalTrials.govother
Study focus
Disease/Condition
Dementia
Drug/Device/Intervention
Nurse-facilitated advance care planning intervention
Study type
Interventional
Intervention type
other
Sponsor & location
Primary sponsor
The University of Hong Kong
Location
Hong Kong, China
Timeline & enrollment
Phase
N/A
Start date
Jun 15, 2023
End date
Nov 30, 2024
Enrollment
120 participants
Primary outcome

Modified Family Member Decision-Making Self-efficacy Scale (FDMSE) - Chinese version,Family Distress in Advanced Dementia Scale (FDAD) - Chinese version

Summary

The goal of this clinical trial is to evaluate the effects of a nurse-facilitated
 post-discharge advance care planning intervention with family surrogates of dementia patients
 on outcomes that reflect the preparedness of surrogates in decision-making.
 
 The main question it aims to answer is, whether the ACP intervention as compared with usual
 care will increase family surrogates' self-efficacy in surrogate decision-making and reduce
 their levels of distress, and increase patient comfort and reduce acute healthcare
 utilization at 2 and 6 months.
 
 Participants will be randomized to ACP intervention vs. usual care.
 
 1. patients of the Intervention group will be assessed on palliative care needs, and
 surrogates of the Intervention group will participate in 2-3 nurse-led ACP
 consultations;
 
 2. surrogates of both intervention and control groups will complete 3 surveys at different
 time points during their participation of the study.
 
 Researchers will compare the intervention group and control group to see any differences in:
 
 1. surrogate preparedness for decision-making,
 
 2. distress of surrogate and satisfaction with the care of loved one with dementia at the
 end-of-life,
 
 3. enrolment in Community Geriatric Assessment Team end-of-life care program,
 
 4. advanced care program documentation in medical record,
 
 5. patient comfort at end-of-life,
 
 6. hospitalizations in the last 6 months of life.

ICD-10 classifications
Unspecified dementiaAlzheimer diseaseDementia in Alzheimer diseaseDementia in Alzheimer disease, unspecifiedDementia in other diseases classified elsewhere
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06152120
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06152120 through Pure Global AI's free database. This phase not specified trial is sponsored by The University of Hong Kong and is currently Enrolling by invitation. The study focuses on Dementia. Target enrollment is 120 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.