N/A
N=640
CommunityRx-Hunger
Food Insecurity
Bottom Line
View on ClinicalTrials.gov: NCT04171999 ↗Enrolled (actual)
640
Serious AEs
0.0%
Results posted
Dec 2024
Primary outcome: Primary: (Aim 1) Caregiver Self-efficacy at 12 Months Among Food Insecure Caregivers — 2; 5; 9; 4 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Community Rx-Hunger (CRx-H) (Other)
- Age
- Pediatric, Adult, Older Adult
- Sex
- All
- Sponsor
- University of Chicago
- Primary completion
- Sep 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY (Aim 1) Caregiver Self-efficacy at 12 Months Among Food Insecure Caregivers |
2; 5; 9; 4; 13; 6 | — |
| PRIMARY (Aim 2) Caregiver Satisfaction With Hospital Discharge |
81.9; 84.2 | — |
Summary
CommunityRx-Hunger (CRx-H) is a hospital-based intervention that addresses food insecurity and other health-related social needs such as transportation, housing, utilities, and safety. Study team members are recruiting caregivers at the time of their child's hospital admission at a large urban children's hospital. For Aim 1, the primary outcome is self-efficacy among food insecure caregivers compared to those who receive the usual standard of care. For Aim 2, the primary outcome is satisfaction with care compared between food secure and food insecure caregivers.
Eligibility Criteria
Inclusion Criteria
- Native English or Spanish speaker
- Living in 1 of 27 zip codes in the study's target region
- Self-identify as a primary caregiver of a child <18 years old hospitalized in a large urban children's hospital
- Ability to send and receive text messages
- Access to a mobile phone and agrees to receive text messages from the study
Exclusion Criteria
- Previous participation in a CRx research study.
- Caregivers of newborns in the hospital
- Patient hospital stay is less than 24 hours
- Patient hospital stay is 30 days or more
- Patient has an eating disorder as indicated in the EMR
Data sourced from ClinicalTrials.gov (NCT04171999). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.