Rehabilitation for People With Advanced Cancer
Contact information
Charmaine Silva, MSc
Princess Margaret Cancer Centre
Princess Margaret Cancer Centre
Basic information
N/A
N/A Age
117 Enrollment
Trial Details
Brief Summary
The proposed study is a Phase II, feasibility, randomized controlled preference based study. This will be conducted in Vancouver and Toronto and includes breast and colorectal cancers.
Official Title
Project 3 - Phase II, Preference Based, Randomized Controlled Trial of Group-Based, In Person Versus Virtual, Cancer Rehabilitation for People With Metastatic / Advanced Breast or Colorectal Cancers
Selection Criteria
Eligibility Inclusion Criteria
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Age 18 years or older
Diagnosed with locally advanced incurable or metastatic breast or colorectal cancer
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
Fully independent with ambulation and transfers with or without ambulatory assistance
Palliative Performance score of >70 (moderate predictive power estimating life expectancy >6 months)
Receiving first or second line anti-cancer treatments in the metastatic / incurable setting (a relative proxy for expected survival >6 months)
Medical clearance to participate from treating physician.
Eligibility Exclusion Criteria
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Wheelchair level community ambulation
Moderate or severe non-cancer pain (>6 out of 10 on visual analog scale)
Moderate or severe cancer bone pain (>Gr 2 bone pain (i.e., moderate pain limiting instrumental ALDs or worse) as measured on CTCAE (see below))
Severe or uncontrolled depressive symptoms (>20 on PHQ-9)
Known neurological conditions influencing cognition and preventing safe or appropriate engagement with self-management and exercise recommendations (e.g., dementia, traumatic brain injury, or brain metastasis influencing cognition or causing moderate-to-severe motor-sensory-coordination). Best determined by the referring physician or nurse practitioner.
Unable to communicate sufficiently in English to complete intervention, questionnaires, and consent.
Unwillingness to be randomized, participate in a group intervention, or attend individual physical assessments.
Inability to operate videoconferencing if preference is virtual programming