Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL (NCT06050850) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL
United States20 participantsStarted 2026-09-01
Plain-language summary
The purpose of this study is to conduct a single arm pilot of the NOURISH-ALL (Nourishing Our Understanding of Role modeling to Improve Support and Health in Acute Lymphoblastic Leukemia) intervention focused on three components of participant engagement. This is a single arm intervention study that involves participation in a 6-session family intervention and three time points of multimethod data collection. The primary outcome is participant engagement, measured as recruitment, retention, and intended dose received.
This study will be conducted over 5 years in three phases:
* Aim 1a: Adapting the NOURISH-ALL Intervention for Families of Youth with ALL (Year 1)
* Aim 1b: Iteratively Refining the NOURISH-ALL Intervention (Year 2)
* Aim 2: Pilot Single-Arm Trial of NOURISH-ALL Focused on Participant Engagement (Years 3-5)
Who can participate
Age range
2 Years – 12 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Children ages 2-12 years old and their primary caregiver ages 18-90
* Child diagnosed with acute lymphoblastic leukemia (ALL)
* Child completed induction phase of therapy and not yet in maintenance phase of therapy
* Primary caregiver and child English language proficient
* Primary caregiver able to provide permission for child to participate in research
* Primary caregiver identifies as being involved with child's oncology care
* Primary caregiver lives with child at least 50% of the time
* Primary oncology provider confirms child is eligible to participate
Exclusion Criteria:
* Primary oncology provider identifies safety concerns regarding the child's participation in the study.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.