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Study identifier: NCT06050850 Synced from ClinicalTrials.gov · August 07, 2026
● Study status: Not Yet RecruitingNOURISH-ALL

Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL

Condition: ALL, Childhood · Behavior, Health  ·  Sponsor: University of Kansas Medical Center

PhaseNA
Planned participants20
Who can joinAll sexes, 2 Years to 12 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where2 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

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)

This description comes directly from the study's public registry record.

Talk to the study team

Carolyn Bates, PhD  ·  913-588-6323  ·  cbates4@kumc.edu

Kelsey M Dean  ·  (816) 652-0065  ·  kdean@kumc.edu

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

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.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (2)

University of Kansas Medical CenterKansas City, Kansas, United States
Children's Mercy Kansas CityKansas City, Missouri, United States

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