No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
12 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
85 (estimated)
Sponsor
St. Jude Children's Research Hospital · Other
Who this trial is looking for
This trial is looking for young cancer patients and their caregivers to share thoughts on how to talk about the impact of cancer on life and future. Participants will help create better ways to communicate about prognosis and life quality.
Are You a Good Fit for This Trial?
You may be able to join if
I am between 12 and 25 years old.
I have a cancer diagnosis that has a poor prognosis.
My doctor estimates my chance of survival is 50% or less.
I have an upcoming disease check with my doctor within six months.
I am not expected to be at end of life in the next three months.
I am a parent or caregiver of a young patient with cancer.
You may not be able to join if
I do not meet the stated inclusion criteria.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
The purpose of this research study is to obtain insights and feedback from patients and parents about a new approach to support conversations about how cancer may affect one's future life and quality of life (i.e., prognostic communication). This study involves creating a personalized approach to discussing prognosis.
Primary Objectives
* To evaluate the feasibility of implementing the RIGHTimeC…
The purpose of this research study is to obtain insights and feedback from patients and parents about a new approach to support conversations about how cancer may affect one's future life and quality of life (i.e., prognostic communication). This study involves creating a personalized approach to discussing prognosis.
Primary Objectives
* To evaluate the feasibility of implementing the RIGHTimeCPV intervention among pediatric oncology patients, caregivers, and clinicians (referred to herein as "shareholders").
* To assess the acceptability of the intervention across the shareholder groups.
Secondary Objectives
* To explore the potential impact of the RIGHTimeCPV intervention on communication quality, concordance in prognostic understanding, and therapeutic alliance between patients/families and multidisciplinary clinicians.
* To explore whether the practice of eliciting, sharing, and honoring individualized communication preferences is sustained by clinicians after participation in the RIGHTimeCPV intervention.
Trial Locations
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City
State
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Status
Eligibility Criteria
Inclusion Criteria: Patients
* Aged 12-25 years diagnosed with poor prognosis cancer (high risk or otherwise difficult to treat cancers), as defined by a pediatric oncologist estimating odds of overall survival as 50% or less
* Anticipated by a pediatric oncologist to have one or more disease re-ev…
Inclusion Criteria: Patients
* Aged 12-25 years diagnosed with poor prognosis cancer (high risk or otherwise difficult to treat cancers), as defined by a pediatric oncologist estimating odds of overall survival as 50% or less
* Anticipated by a pediatric oncologist to have one or more disease re-evaluation timepoints over the next six months
* Not anticipated by a pediatric oncologist to approach end of life in the next three months
Inclusion Criteria: Parents/Caregivers
* Aged 18 years or older and/or legally emancipated
* Parent or other self-identified caregiver of a patient of any age with poor prognosis cancer (as defined above)
Inclusion Criteria: Oncologists
* Pediatric oncologists who treat eligible patients/caregivers at the study site, St. Jude Children's Research Hospital (SJCRH) or its included affiliates:
* Peoria, IL: The Jim and Trudy Maloof St. Jude Midwest Affiliate Clinic
* Charlotte, NC: Novant Health Hemby Children's Hospital
* Shreveport, LA: Ochsner LSU Health-Feist-Weiller Cancer Center
Inclusion Criteria: Communication Preferences Companions (CPCs)
* Multidisciplinary clinicians from a participant's psychosocial or nursing care team, identified by that participant to serve as their 'communication preferences companion' (CPC) during the pilot
* Provides clinical care to pediatric cancer patients under the auspices of psychology, social work, spiritual care, child life, cultural navigation, quality of life/palliative care, or nursing
Exclusion Criteria:
* Does not meet the stated inclusion criteria
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