Actively Recruiting
Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL
Led by University of Kansas Medical Center · Updated on 2025-10-24
46
Participants Needed
2
Research Sites
310 weeks
Total Duration
On this page
Sponsors
U
University of Kansas Medical Center
Lead Sponsor
C
Children's Mercy Hospital Kansas City
Collaborating Sponsor
AI-Summary
What this Trial Is About
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)
CONDITIONS
Official Title
Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Children ages 2 to 12 years and their primary caregiver ages 18 to 90
- Child diagnosed with acute lymphoblastic leukemia (ALL)
- Child has completed the induction phase of therapy and is not yet in the maintenance phase
- Primary caregiver and child are proficient in English
- Primary caregiver can provide permission for the child to participate in research
- Primary caregiver is involved in the child's oncology care
- Primary caregiver lives with the child at least 50% of the time
- Primary oncology provider confirms the child is eligible to participate
You will not qualify if you...
- Primary oncology provider identifies safety concerns regarding the child's participation in the study
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 2 locations
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Active, Not Recruiting
2
Children's Mercy Kansas City
Kansas City, Missouri, United States, 64118
Actively Recruiting
Research Team
C
Carolyn Bates, PhD
CONTACT
K
Kelsey M Dean
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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