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Implementation Strategy - Intervention Condition for Food Insecurity
N/A
Waitlist Available
Research Sponsored by Temple University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* A 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 control condition
Timeline
Screening 3 weeks
Treatment Varies
Follow Up after 1 year; after 2 years of the trial
Awards & highlights
Summary
The purpose of this study is to assess the impact of an implementation strategy on participation in Universal School Meals (USM).
Eligible Conditions
- Food Insecurity
- Childhood Obesity
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ after 1 year of the trial
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~after 1 year of the trial
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Implementation Cost Measure
Implementation Mapping Self-Assessment
Implementation Outcomes Surveys
+2 moreSecondary study objectives
Dietary Behaviors
Food Insecurity
Height
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Implementation Strategy - Intervention ConditionExperimental Treatment1 Intervention
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 in the following academic years (2- year pilot).
Group II: Waitlist ControlActive Control1 Intervention
Schools in the waitlist control will wait 1 academic year before developing and testing an implementation strategy (1-year pilot)
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Who is running the clinical trial?
Temple UniversityLead Sponsor
304 Previous Clinical Trials
85,665 Total Patients Enrolled
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