Improving Participation in Universal School Meals (USM)

Temple University

Status: Active, not recruiting

Conditions: Obesity, Childhood; Food Deprivation

Treatments: Other: Waitlist Comparison - Implementation Mapping; Other: Implementation Mapping

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT06579079

#28959

Details and patient eligibility

About

The purpose of this study is to assess the impact of an implementation strategy on participation in Universal School Meals (USM).

Full description

The purpose of this cluster randomized trial is to test the effectiveness of an implementation strategy on implementation and student health outcomes of universal school meals (USM). This will be completed by developing and tailoring of an implementation strategy and testing its effectiveness though a cluster randomized design. Primary implementation outcomes of this trial are acceptability, cost, feasibility, penetration, and sustainability. Secondary student health outcomes are changes in diet quality (district-wide survey for students), food insecurity (USDA 6-item screener), and weight status. Exploratory descriptive models will be run to assess differences between intervention and control schools. To provide evidence for approaches in adolescents at highest risk for poor dietary intake, food security, and obesity risk, racial and ethnic minority adolescents from the School District of Philadelphia will comprise the majority of the sample. The principal investigator has just completed a year-long needs assessment with 8 schools across the district. We will aim to recruit 4 schools to be randomized to 1 of 2 conditions. Recruitment is underway, final recruitment details will be added once randomization is complete. From these schools, we aim to randomize (2 intervention; 2 waitlist comparison) for the development and tailoring of an implementation strategy. At baseline and throughout the 2-year trial period, we aim to collect interview data and surveys, and analyze data on diet quality, food security, and weight status.

Enrollment: 1,000 estimated patients

Sex: All

Ages: 11 to 99 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• An elementary/middle or high school within the School District of Philadelphia (SDP) that provides free breakfast and lunch to students
• School is willing to be randomized to either a treatment or waitlist comparison condition
• School has a team of teachers, administration, and food service staff who are willing to complete interviews and surveys for data collection
• School has valid data for student Body Mass Index, meal participation, and food insecurity (parent reported).
• Students currently enrolled in a SDP elementary/middle/high school
• Students willing to participate in an interview and complete surveys
• Students have participated in school meals in the last year.

Exclusion criteria

• Charter schools and private schools
• Students not enrolled in school full time; students under 11 years of age.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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1,000 participants in 2 patient groups

Implementation Strategy - Intervention Condition

Experimental group

Description:

Schools in the intervention condition will be assigned to receive coaching and logistical support to develop and tailor an implementation strategy across 1 academic year. This strategy will then be implemented gradually and in the following academic years (2- year pilot).

Treatment:

Other: Implementation Mapping

Waitlist Control

Active Comparator group

Description:

Schools in the waitlist control will wait 1 academic year before developing and testing an implementation strategy (1-year pilot)

Treatment:

Other: Waitlist Comparison - Implementation Mapping