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The Calgary Movement Disorders Advanced Care Pilot Program (ACT for PD)

U

University of Calgary

Status

Not yet enrolling

Conditions

Parkinson's Disease and Parkinsonism

Treatments

Behavioral: Palliative care

Study type

Interventional

Funder types

Other

Identifiers

NCT05599659
REB22-0545

Details and patient eligibility

About

The goal of this clinical trial is to analyse the effect of palliative care interventions on quality of life, patient satisfaction, carepartner burden and health care utilization patterns in patients living with parkisonism and their carepartners.

Participants will:

  • Receive multidisciplinary palliative care.
  • Answer questions related to the quality of life, patient satisfaction, carepartner burden and health care utilization patterns.

Enrollment

100 estimated patients

Sex

All

Ages

20 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants who have a PD diagnosis or another PDRD diagnosis (multiple system atrophy, corticobasal degeneration, progressive supranuclear palsy, or Lewy body dementia)
  • Participants who have moderate to high PC needs based on the Palliative Care Needs Assessment Tool (PC-NAT)
  • Participants who are between 20 and 100 years old

Exclusion criteria

  • Immediate and urgent palliative care needs. These patients will be offered appropriate services immediately
  • Participants who have other illnesses that could require PC e.g. metastatic cancer
  • Participants already receiving PC and/or hospice
  • Patients with a diagnosis of severe cognitive impairment (Montreal Cognitive Assessment <10). These patients will be offered appropriate services. Care partners can participate.

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

100 participants in 1 patient group

Palliative care
Experimental group
Description:
Participants will receive palliative care.
Treatment:
Behavioral: Palliative care

Trial contacts and locations

1

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Central trial contact

Veronica Bruno, MD, MPH; Karla Cantu Flores, MD

Data sourced from clinicaltrials.gov

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