Actively Recruiting
Comprehensive Health Assessment for My Plan: Initial Implementation Study (CHAMP Implementation Study)
Led by University of Toronto · Updated on 2025-03-28
210
Participants Needed
1
Research Sites
71 weeks
Total Duration
On this page
Sponsors
U
University of Toronto
Lead Sponsor
U
University Health Network, Toronto
Collaborating Sponsor
AI-Summary
What this Trial Is About
The current standard preoperative assessment does not consider the needs of older adults undergoing non-oncological surgery. To enhance the treatment decision-making and planning for older adult surgical patients, the British Geriatric Society and the American Society of Colon and Rectal Surgeons recommend the implementation of preoperative GA for all older adults. Geriatric assessment (GA) predicts treatment toxicity and overall mortality in older adults with complex health problems. However, in-person GA may not be feasible in several clinical settings for various reasons, including lack of training, time, or access to advanced geriatric services. These challenges can be minimized through a self-reported online GA that can be completed by patients prior to the participants' medical appointment. In a previous study, the investigators developed a self-reported online GA, known as the Comprehensive Health Assessment for My Cancer treatment Plan (CHAMP), which was used in geriatric oncology to increase accessibility to GA for older adults with cancer. In this study, the aim is to deploy the CHAMP tool to various clinics across 4 institutions and assess feasibility outcomes, as well as the efficacy of the CHAMP tool in the identification of geriatric issues and the development of supportive care.
CONDITIONS
Official Title
Comprehensive Health Assessment for My Plan: Initial Implementation Study (CHAMP Implementation Study)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged 70 years old and over who have been referred to any kind of non-oncological surgery
- Able to speak English
- Able to provide informed consent
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
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Trial Site Locations
Total: 1 location
1
University Health Network
Toronto, Ontario, Canada, M5G2C4
Actively Recruiting
Research Team
M
Martine Puts, PhD RN
CONTACT
S
Shabbir Alibhai, MD MSc
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
1
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