Actively Recruiting

Phase Not Applicable
Age: 70Years +
All Genders
ID06464471

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

Led by University of Toronto · Updated on 2025-03-28

210

Participants Needed

1

Research Sites

30 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

Researchers are evaluating the use of a self-reported online geriatric assessment tool called CHAMP to improve preoperative evaluation and care planning for older adults aged 70 years and above undergoing non-cancer related surgery. The study aims to address the lack of tailored assessments for this population, as current standard preoperative evaluations often overlook important health and functional issues common in older adults. The CHAMP tool was developed to increase accessibility to geriatric assessment and assist clinicians in identifying geriatric issues and planning supportive care. Participants in this study will complete the CHAMP tool either at home via the internet or in clinic using an iPad before their medical appointment. The tool covers multiple health domains such as function, mobility, cognition, nutrition, social support, depression, and substance use, and takes about 10 to 15 minutes to complete. After the participants fill out the tool, results are shared with their clinician to inform treatment decisions. Surveys will assess satisfaction with the tool from both patients and physicians. Throughout the study, participants will provide information about their demographics and comfort with technology, complete the CHAMP tool before consultation, and then attend their clinician appointment. About one week after the consultation, participants will complete questionnaires regarding their experience with the CHAMP tool. Researchers will measure the completeness and time taken to fill out the tool, satisfaction levels, changes in proposed treatment plans, and supportive care strategies. The study will help determine the feasibility and effectiveness of the CHAMP tool in improving preoperative care for older surgical patients.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 70Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or remote) for consent and eligibility assessment

Implementation of the CHAMP Tool

Duration - Within 1 week before the medical appointment

Participants complete the self-reported online CHAMP geriatric assessment tool at home or in the clinic prior to their medical appointment to help identify geriatric issues and inform treatment decisions.

1 baseline visit (in-person or remote) for completing questionnaires and the CHAMP tool before the medical appointment

Medical Consultation

Duration - 1 day

Participants meet with the clinician who reviews the CHAMP tool results and discusses the treatment plan and any modifications based on the assessment.

1 medical appointment (in-person)

Post-Consultation Follow-up

Duration - Approximately 1 week

Participants complete questionnaires about their experience and satisfaction with the CHAMP tool approximately one week after the medical consultation.

1 follow-up visit (remote or in-person) to complete satisfaction surveys

Trial Site Locations

Total: 1 location

1

University Health Network

Toronto, Ontario, Canada, M5G2C4

Actively Recruiting

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Research Team

M

Martine Puts, PhD RN

S

Shabbir Alibhai, MD MSc

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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