Cognitive Function Informed Care for Mental Health
(CFIC Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
Cognitive Function Informed Care (CFIC) is a new, add-on type of care for mental health outpatients. To receive this type of care, a child/youth does something called a neuropsychological assessment, which are tests given by a special type of psychologist, called a neuropsychologist. These tests give the neuropsychologist information about how that child/youth's brain works, in a way that is unique to them. This information is called cognitive function, and it is shared with the patient and their family. This information is also shared with their mental health provider, who will work with the neuropsychologist to make sure that their treatment makes sense for their brain.
One main purpose of this research is to see if it is better to receive information about cognitive function to help make treatment decisions (CFIC), or better to receive standard care without this information. To do this, participants will be randomly assigned to either receive CFIC or proceed with standard care. Between groups, we will be comparing any improvement(s) in overall function and symptoms.
The other main purpose of this research is to evaluate how CFIC influences the outpatient mental health service (i.e., implementation). We will be monitoring how the service is delivered, documenting changes as needed, asking patients about their experience(s), surveying staff members and evaluating cost.
Are You a Good Fit for This Trial?
This trial is for children and youth receiving outpatient mental health care. Participants must be able to complete neuropsychological assessments and work with their families and providers. There are no detailed exclusion criteria listed.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Cognitive Function Informed Care (CFIC)
Trial Overview
The study compares a new approach called Cognitive Function Informed Care (CFIC), which uses brain function testing to guide treatment, against standard mental health care. Participants are randomly assigned to either group.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Participants will receive a neuropsychological assessment before treatment. Results from this assessment will be interpreted and applied to their treatment plan.
The TAU group will proceed with the standard mental health care path. Once post-test measures are complete, these participants will receive a neuropsychological assessment.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Children's Hospital of Eastern Ontario
Lead Sponsor
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.