Your session is about to expire
← Back to Search
Lay Navigator Intervention for End of Life (CAREPlan Trial)
N/A
Waitlist Available
Research Sponsored by Stanford University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 12 months after patient enrollment
Awards & highlights
CAREPlan Trial Summary
This trial is testing if a layperson can help cancer patients with advance care planning, to improve patient activation, satisfaction, quality of life, and the quality of end of life cancer care.
Eligible Conditions
- End of Life
- Cancer
CAREPlan Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 12 months after patient enrollment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~12 months after patient enrollment
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Goals of Care Documentation
Secondary outcome measures
Emergency Department Visit using chart abstraction
Hospice using chart abstraction
Hospitalization Visit using chart abstraction
+1 moreCAREPlan Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Intervention Group ArmExperimental Treatment2 Interventions
Patients randomized into the intervention will be assigned a lay patient navigator who will provide information regarding early advance care planning, documentation of goals of care, and coordinating home-based care. The intervention arm will also receive usual care as provided by their local oncologists.
Group II: Control Group ArmActive Control1 Intervention
The control group will receive usual care as provided by their local oncologists.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Lay Navigator Intervention
2019
N/A
~400
Find a Location
Who is running the clinical trial?
Stanford UniversityLead Sponsor
2,408 Previous Clinical Trials
17,342,807 Total Patients Enrolled
5 Trials studying End of Life
4,601 Patients Enrolled for End of Life
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Control Group Arm
- Group 2: Intervention Group Arm
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Share this study with friends
Copy Link
Messenger