Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL
Part of paid clinical trials in Kansas City, Kansas.
- Sponsor
- University of Kansas Medical Center
- Study ID
- NCT06050850
- Status
- Not Yet Recruiting
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Conditions
- ALL, Childhood
- Behavior, Health
Eligibility Criteria
- Sex
- ALL
- Age
- 2 Years - 12 Years
- Healthy Volunteers
- Not accepted
Interventions
- NOURISH-ALL — BEHAVIORALOur NOURISH-ALL intervention will build on this existing NOURISH-T family based behavioral intervention with families of cancer survivors. The intervention, NOURISH-ALL, will adapt these family-based health promotion strategies to the early ALL treatment context.
Study Details
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)
Key Dates
- First listed
- Sep 22, 2023
- Start date
- Sep 1, 2026
- Status verified
- Oct 2025
- Primary completion
- Sep 1, 2028
- Completion
- Sep 1, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- PREVENTION
Arms
- Experimental: Aim 2: Pilot Single-Arm Trial of NOURISH-ALL Focused on Participant Engagement (Years 3-5)Pilot testing key components of engagement is critical to optimizing design and methodology of fully powered efficacy trials. The purpose of Aim 2 is to pilot a single-arm trial of the finalized NOURISH-ALL intervention in a sample of families of youth in the early phases of ALL treatment to assess recruitment, retention, and dose received. Results will directly inform the design of the fully powered randomized control trial to test intervention efficacy (R01 application to be submitted in Year 4).
Primary Outcome Measure
Recruitment Rate [ Time Frame: Baseline (Week 0) ]
Central Contacts
- Carolyn Bates, PhD913-588-6323
- Kelsey M Dean(816) 652-0065
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Kansas Medical Center | Kansas City | Kansas | 66160 | - |
| Children's Mercy Kansas City | Kansas City | Missouri | 64118 | Keith August, MD (PRINCIPAL_INVESTIGATOR) |
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