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Clinical Trials/NCT04162912
NCT04162912
Completed
Not Applicable

Effects of a Motivational Interviewing Tailored Programme for Promoting Advance Care Planning Behaviours Among Patients With Palliative Care Needs: A Randomised Controlled Trial

Food and Health Bureau, Hong Kong2 sites in 1 country204 target enrollmentJanuary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
End Stage Disease
Sponsor
Food and Health Bureau, Hong Kong
Enrollment
204
Locations
2
Primary Endpoint
Advance Care Planning Behaviour
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

This proposed study is designed to test the effects of motivational interviewing (MI) in increasing the uptake of ACP behaviours among patients with palliative care needs. A randomised controlled trial with repeated blinded outcome assessment will be conducted to assess the effects of a MI-tailored ACP (MI-ACP) programme on palliative care patients recruited from the outpatient palliative care clinics and home palliative care services of two hospitals. A total of 204 patients will be recruited and randomly assigned to experimental and control groups. The patients in the experimental group will receive a MI-ACP programme facilitated by a trained nurse, whereas the patients in the control group will receive usual care. Primary outcome is the behavioural changes in ACP. Secondary outcomes are perceived stress, decisional conflict and quality of life. Study outcomes will be measured at baseline, 1 month and 3 months after enrolment.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
December 31, 2019
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Food and Health Bureau, Hong Kong
Responsible Party
Principal Investigator
Principal Investigator

Dr. Helen YL Chan

Associate Professor

Chinese University of Hong Kong

Eligibility Criteria

Inclusion Criteria

  • 18 years of age or over
  • newly referred to palliative care services
  • with a palliative performance scale (PPS) score of 60 or above; and
  • with full level of consciousness

Exclusion Criteria

  • uncommunicable because of sensory impairment or language barrier
  • cognitively impaired
  • are receiving active psychiatric treatment
  • already had signed an advance directive

Outcomes

Primary Outcomes

Advance Care Planning Behaviour

Time Frame: Baseline, 1 month and 3 months follow up

Behaviour changes in ACP behaviours measured using a questionnaire. It included 4 items about different ACP behavior on a 5-point Likert scale. The higher score means the higher level of readiness for the behaviours.

Secondary Outcomes

  • Perceived stress(Baseline, 1 month and 3 months follow up)
  • Quality of life(Baseline, 1 month and 3 months follow up)
  • Decisional conflict(Baseline, 1 month and 3 months follow up)

Study Sites (2)

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