CClinicalTrials.gg
Status unknownNCT03267706Updated Aug 30, 2017

Introducing the Palliative Care Comprehensive Tool in Family Medicine

An interventional study of Palliative Care Comprehensive Tool in Palliative Care, Primary Care and Satisfaction, sponsored by McMaster University. Status unknown at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-08-30.

Sponsored by McMaster University · Not applicable, Interventional, and Supportive care

The sponsor has not verified this record recently (last verified Aug 2017), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
149
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to pilot the introduction of a newly developed palliative care tool to clinicians in a family health team. The intent of the tool is to improve the quality and comprehensiveness of palliative care, which effects caregiver and patient satisfaction with care received, as well as clinician satisfaction with their delivery of care. Tool effectiveness will be evaluated by measuring satisfaction scores of caregivers, patients and clinicians who receive training and access to the tool compared to caregivers, patients and clinicians providing usual care (without the tool). Uptake of the tool and user feedback will be collected

Read the detailed description

A newly developed tool to guide clinicians in best palliative care practices was developed based on a combination of published tools and consultation with primary care, end users (clinicians). The tool will be introduced as a pilot to clinicians who will receive training on use of the tool and access to the tool within a family health team in Ontario, Canada. The tool will be applied in a controlled study environment that randomly assigns clinicians to one of two groups. One group will receive training and access to the tool and the other group of clinicians will continue to provide usual care.The tool will be evaluated based on validated satisfaction surveys completed by caregivers, patients and clinicians. Satisfaction scores of those randomly assigned to care enhanced by the tool will be compared to those receiving usual care at the beginning and end of the study. Uptake of the tool will be measured, as well as user experience with the tool (feasibility and acceptability)

02

Conditions studied

  • Palliative Care
  • Primary Care
  • Satisfaction

Keywords

  • Primary care
  • Palliative care
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Inclusive sample of all clinicians employed at Stonechurch Family Health Centre
  • Inclusive sample of all patients over 18 years of age, registered as palliative within Stonechurch Family Health Centre and who are English speaking

Exclusion Criteria: Patients younger than 18 years of age, patients who are non-English speaking

-

04

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
149 participants (estimated)

Study arms

  • Active comparator
    Palliative Care Comprehensive Tool

    Clinicians within the study will be randomly assigned and trained on the use of the Palliative Care Comprehensive Tool

    Other: Palliative Care Comprehensive Tool

  • No intervention
    Usual Care

    Clinicians within the study will be randomly assigned to usual palliative care (without the newly introduced tool)

Interventions

  • OtherPalliative Care Comprehensive Tool

    Clinicians assigned to the newly developed Palliative Care Comprehensive Tool will be trained during a 1 hour period on the application of the tool; Including rationale for tool development, objective of the tool and demonstration of the tool in action

    Also known as: PaCCT

05

What researchers measure

Primary outcomes

  1. Caregiver satisfaction

    FAMCARE-2 survey to measure caregiver satisfaction

    Time frame: 3 months

Secondary outcomes

  1. Patient satisfaction

    FAMCARE-P13

    Time frame: 3 months

  2. Clinician satisfaction

    Physician Satisfaction with Aspects of Chronic Care (modified)

    Time frame: 3 months

  3. User feedback

    Acceptability and feasibility of the Palliative Care Comprehensive Tool will be sought using the Clinical Sensibility Questionnaire

    Time frame: 3 months

  4. Uptake of tool

    Tool implementation will be (rate of tool uptake by clinician)

    Time frame: 3 month

06

Study locations

1 site
  • Stonechurch Family Health Centre, Department of Family Medicine McMaster University
    Hamilton, Ontario L8W3J6, Canada
    • Sarah Xu, MD · Contact · sarah.xu@medportal.ca · 9055751300
    • Amanpaul Bhamber, MD · Contact · amanpaul.bhamber@medportal.ca · 9055751300
    • Ainsley Moore, MD · Principal investigator
    • Sarah Xu, MD · Sub investigator
    • Amanpaul Bhamber, MD · Sub investigator
    • Amanda Ramdyal, MD · Principal investigator
07

References and documents

Individual participant data

Plan to share: No — No plan to share data. Data will be stored on secured facility servers.

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03267706
Lead sponsor
McMaster University
Responsible party
Ainsley Moore (Associate Professor of Family Medicine, McMaster University) — Principal investigator
First posted
Aug 30, 2017
Start date
Sep 2017 (estimated)
Primary completion
Mar 2018 (estimated)
Completion
Jun 2018 (estimated)
Last update
Aug 30, 2017

Study contacts

Sarah Xu, MD
Contact
sarah.xu@medportal.ca
9055751300
Amanpaul Bhamber, MD
Contact
amanpaul.bhamber@medportal.ca
9055751300
Ainsley Moore, MD
principal investigator · Department of Family Medicine McMaster University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2017. You cannot join it, but the record below documents what was studied.

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