NCT06090240

Brief Summary

This study aims to evaluate the effectiveness of a motivational interviewing (MI) intervention in enhancing advance care planning (ACP) among older adults who have visited the Emergency Room (ER) in the past six months and their family caregivers. The main question it aims to answer is: The effectiveness of the MI-based ACP intervention implemented within six months of an ER visit on improving older adults' advance directives (AD) completion rate. Compared to participants in the control group who will only receive a self-education booklet, participants in the intervention group will receive a motivational interview educational intervention to see the effectiveness of an MI-based ACP intervention implemented within six months following an emergency room visit regarding the completion of AD for older adults.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
376

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Oct 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

First Submitted

Initial submission to the registry

October 13, 2023

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 19, 2023

Completed
1 day until next milestone

Study Start

First participant enrolled

October 20, 2023

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
Last Updated

June 29, 2025

Status Verified

June 1, 2025

Enrollment Period

1.8 years

First QC Date

October 13, 2023

Last Update Submit

June 25, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Older adults' readiness for ACP

    Older adults' readiness for ACP (primary outcome) will be measured by the readiness subscales of the Advance Care Planning Engagement Survey (ACPES), which comprises 6 items rated on a 5-point Likert scale, ranging from 1 (worst outcome) to 5 (best outcome). A higher score indicates a higher readiness for ACP. It assesses an individual's readiness to sign official papers for health decision delegates and ADs and readiness to talk with family and physicians about EOL care, and has been validated in Hong Kong.

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months (T3) post intervention.

Secondary Outcomes (8)

  • Family caregivers' readiness for ACP

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months (T3) post intervention.

  • Older adults' emotional perception of ACP

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months (T3) post intervention.

  • Older adults' and family caregivers' decisional conflict

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months (T3) post intervention.

  • Older adults and family caregivers' congruence in goal of EOL care

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months (T3) post intervention.

  • Older adults' completion of AD documentation

    before the intervention (T0), and 3-month (T1), 6-month (T2), and 12-months(T3) post intervention .

  • +3 more secondary outcomes

Study Arms (2)

Motivational Interview

EXPERIMENTAL

Older adult-family member dyads in this arm will receive an MI-based education intervention our team developed.

Other: MI-based ACP intervention

Self-learning

NO INTERVENTION

Older adult-family member dyads in this arm will receive a self-learning ACP educational material developed by the Hong Kong Hospital Authority.

Interventions

Motivational Interviewing on Advance Care Planning Intervention: Dyads of older adults and family caregivers will receive three MI-based ACP counselling sessions: (1) a preparatory session, (2) motivation session, and (3) planning session. The preparatory session will take 10-15 minutes, and the following two sessions in weeks 2 and 3 will last 30-45 minutes each. Before each session, the nurse interventionist will first assess the dyad's readiness to engage in ACP based on the state of change algorithm. Participants who have never thought about ACP will be in the pre-contemplation state, those who are willing to discuss EOL care and preferences to be in the contemplation state, those ready to talk about EOL planning to be in the preparation state, and those in the action state have a confirmed action plan on signing up their ADs. Readiness-based ACP goals will be established, and state-matched MI counseling will be customized for each participant.

Motivational Interview

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Aged 65 or older
  • At least one episode of ER visit in the last six months
  • Has a family caregiver to be present during the intervention
  • Able to communicate in Chinese

You may not qualify if:

  • Has completion of an AD
  • Moderate to severe cognitive impairment or diagnosis of dementia, as identified in health records
  • Communication problems (e.g., deafness or aphasia)
  • For family caregivers:
  • Aged 18 or above
  • Immediate or extended family member or friend nominated by an eligible older adult participant as primary caregiver
  • Able to communicate in Chinese
  • Moderate to severe cognitive impairment
  • Communication problems (e.g., deafness or aphasia)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Hong Kong, School of Nursing

Hong Kong, Hong Kong

RECRUITING

Study Officials

  • Chia-Chin LIN, PhD,FAAN,RN

    University of Hong Kong, School of Nursing

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Chia-Chin LIN, PhD,FAAN,RN

CONTACT

Tongyao Wang, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 13, 2023

First Posted

October 19, 2023

Study Start

October 20, 2023

Primary Completion

July 31, 2025

Study Completion

July 31, 2025

Last Updated

June 29, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations