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Motivational Interviewing Tailored Programme for Promoting Advance Care Planning Behaviours

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04162912
Enrollment
204
Registered
2019-11-14
Start date
2018-01-01
Completion date
2019-12-31
Last updated
2020-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

End Stage Disease

Keywords

Advance Care Planning, Motivational Interviewing, Pallative Care

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.

Interventions

BEHAVIORALMotivational Interviewing tailored Advance Care Planning

The trained interventionist who is experienced in MI techniques will explore their illness experiences, emotions and beliefs about their health conditions and future care in an empathetic manner and explore their ambivalence for ACP behaviours.

Sponsors

Haven of Hope Hospital
CollaboratorOTHER
United Christian Hospital
CollaboratorOTHER
Food and Health Bureau, Hong Kong
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Advance Care Planning BehaviourBaseline, 1 month and 3 months follow upBehaviour 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

MeasureTime frameDescription
Decisional conflictBaseline, 1 month and 3 months follow upDecisional conflict regarding end-of-life care is measured by the SURE test, a questionnaire with 4-item on knowledge and support for medical decision making. The higher score means the less decisional conflict.
Perceived stressBaseline, 1 month and 3 months follow upPerceived stress is measured by a 10-item Perceived Stress Scale, a questionnaire, using a 5-point Likert scale. The higher score means the higher level of stress.
Quality of lifeBaseline, 1 month and 3 months follow upQuality of life is measured by using a 23-item modified Quality of Life Concerns in the End of Life Questionnaire. The 23 items are rated on a 4-point Likert scale. The higher score means the better quality of life.

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026