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Randomized Control Trial of Advance Care Planning in Primary Care

Primary Purpose

Chronic Illness

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Advance care planning education session
Wait list control
Sponsored by
McMaster University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Chronic Illness focused on measuring Substitute decision makers of patient

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients being treated for serious illness in outpatient settings or;
  • Patients who could benefit from advance care planning self-assessed or assessed by their physician
  • Patient able and willing to identify a substitute decision-maker who will participate in the study
  • Patient cognitively able to participate

Exclusion Criteria:

  • Patient or their substitute decision-maker does not speak English
  • Patient unable to identify a substitute decision-maker who will consent to participation
  • Patient does not consent to participation

Sites / Locations

  • Dundas Family Health Team
  • Michael West Doctor Office
  • Burlington Family Health Team
  • St. Joseph's Healthcare Hamilton
  • McMaster Family Health Team
  • McMaster University Medical Centre
  • Juravinski Cancer Centre Pain and Symptom Management Team

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Advance care planning education session

Wait list control

Arm Description

Delivery of an advance care planning education session at the family doctor's office

The intervention is not provided.

Outcomes

Primary Outcome Measures

Advance care planning engagement of substitute decision-maker
A survey of the substitute decision-maker's engagement in advance care planning

Secondary Outcome Measures

Advance care planning engagement of patient
A survey of the patient's engagement in advance care planning
Substitute decision-maker self-efficacy survey
A survey of the substitute decision-maker's confidence to make future decisions
Decisional conflict
A modified short decisional conflict survey
Satisfaction with intervention
A satisfaction and endorsement survey on the process of the educational intervention

Full Information

First Posted
August 2, 2017
Last Updated
February 19, 2020
Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR), Queen's University
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1. Study Identification

Unique Protocol Identification Number
NCT03239639
Brief Title
Randomized Control Trial of Advance Care Planning in Primary Care
Official Title
A Randomized Control Trial of an Advance Care Planning Intervention to Engaged Substitute Decision-makers in Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
March 1, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR), Queen's University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Sometimes people with health conditions become ill suddenly and can no longer speak for themselves and another person (such as a family member) will make health care decisions for them. This means it is important to think about your wishes and tell others about them. This is called advance care planning. When people have done advance care planning, if they become very sick and cannot speak for themselves they are more likely to get the kind of health care they want and it is easier for the people who make decisions for them. There are tools such as brochures, questionnaires, and videos that can help people learn about these things. This research is being to done to study whether using tools for advance care planning and goals of care discussions will improve how patients and their substitute decision makers do advance care planning. This study is a randomized trial. This means half of the people in this study will meet with someone at their family practice to talk about advance care planning and review some tools and half will get usual care (a Speak Up workbook). The study will 1) evaluate if reviewing the tools, and having help to complete them, helps patients and their substitute decision maker do advance care planning 2) if this intervention will encourage patients to talk to their family doctor about these issues.
Detailed Description
In prospective and randomized trials, advance care planning (ACP) significantly improves outcomes including increased likelihood that clinicians and families understand and comply with a patient's wishes, reduces hospitalization at the end of life, results in less intensive treatments at the end of life (according to patients' wishes) and increases use of hospice services. Trials have not been done in primary care. In this project, we aim to determine the efficacy of a care pathway designed to increase the quality and quantity of ACP in patients and their substitute decision-makers in primary care. The study is a multi-site, patient-based, unblinded, randomized trial conducted in family practices in Canada. Participants will be patients who are determined by their physician to be able to benefit from ACP, and the patient's substitute decision-maker. Participant pairs will be randomized to immediate intervention (care pathway) or delayed (8-12 weeks). The intervention is guided use of tools and decision aids to clarify values and preferences for treatments in the event of serious illness or near end of life. The outcomes will be substitute decision-maker engagement in ACP (including self-efficacy for enacting the role), patient engagement in ACP, and decisional conflict.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Illness
Keywords
Substitute decision makers of patient

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants are assigned in 1:1 ratio to intervention or wait list control group
Masking
None (Open Label)
Allocation
Randomized
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Advance care planning education session
Arm Type
Experimental
Arm Description
Delivery of an advance care planning education session at the family doctor's office
Arm Title
Wait list control
Arm Type
Sham Comparator
Arm Description
The intervention is not provided.
Intervention Type
Behavioral
Intervention Name(s)
Advance care planning education session
Intervention Description
Administration of values clarification tool, elicitation of preference for treatment options, if preference for resuscitation, shown an educational video about cardiopulmonary resuscitation, summary document of values and preferences created by a facilitator to share with doctor
Intervention Type
Other
Intervention Name(s)
Wait list control
Intervention Description
No intervention
Primary Outcome Measure Information:
Title
Advance care planning engagement of substitute decision-maker
Description
A survey of the substitute decision-maker's engagement in advance care planning
Time Frame
8 to 12 weeks (6 weeks for patients from cancer centre)
Secondary Outcome Measure Information:
Title
Advance care planning engagement of patient
Description
A survey of the patient's engagement in advance care planning
Time Frame
8 to 12 weeks (6 weeks for patients from cancer centre)
Title
Substitute decision-maker self-efficacy survey
Description
A survey of the substitute decision-maker's confidence to make future decisions
Time Frame
8 to 12 weeks (6 weeks for patients from cancer centre)
Title
Decisional conflict
Description
A modified short decisional conflict survey
Time Frame
immediately after intervention
Title
Satisfaction with intervention
Description
A satisfaction and endorsement survey on the process of the educational intervention
Time Frame
immediately after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients being treated for serious illness in outpatient settings or; Patients who could benefit from advance care planning self-assessed or assessed by their physician Patient able and willing to identify a substitute decision-maker who will participate in the study Patient cognitively able to participate Exclusion Criteria: Patient or their substitute decision-maker does not speak English Patient unable to identify a substitute decision-maker who will consent to participation Patient does not consent to participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle Howard, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dundas Family Health Team
City
Dundas
State/Province
Ontario
Country
Canada
Facility Name
Michael West Doctor Office
City
Dundas
State/Province
Ontario
Country
Canada
Facility Name
Burlington Family Health Team
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L7S 0A1
Country
Canada
Facility Name
St. Joseph's Healthcare Hamilton
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8N 4A6
Country
Canada
Facility Name
McMaster Family Health Team
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8P 1H6
Country
Canada
Facility Name
McMaster University Medical Centre
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 4K1
Country
Canada
Facility Name
Juravinski Cancer Centre Pain and Symptom Management Team
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8V 5C2
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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Citation
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Description
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Randomized Control Trial of Advance Care Planning in Primary Care

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