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Study identifier: NCT06464471 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Comprehensive Health Assessment for My Plan: Initial Implementation Study (CHAMP Implementation Study)

Condition: Cancer · Older Adults  ·  Sponsor: University of Toronto

PhaseNA
Planned participants210
Who can joinAll sexes, 70 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Martine Puts, PhD RN  ·  416-978-6059  ·  martine.puts@utoronto.ca

Shabbir Alibhai, MD MSc

Always discuss trial participation with your own doctor first.

Locations (1)

University Health NetworkToronto, Ontario, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06464471