High-Stress Intervention for Food Insecurity

Phase-Based Progress Estimates
1
Effectiveness
1
Safety
Food InsecurityHigh-Stress Intervention - Behavioral
Eligibility
18+
All Sexes
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Study Summary

This trial will study the relationship between food insecurity and stress-induced eating in 400 people in Los Angeles.

Treatment Effectiveness

Study Objectives

1 Primary · 0 Secondary · Reporting Duration: Hyperpalatable food intake will be measured immediately after the intervention.

Hyperpalatable food intake will be measured immediately after the intervention.
Hyperpalatable Food Intake Measured in Kilocalories

Trial Safety

Trial Design

2 Treatment Groups

Control Arm
1 of 2
Experimental (High-Stress) Arm
1 of 2

Active Control

Experimental Treatment

400 Total Participants · 2 Treatment Groups

Primary Treatment: High-Stress Intervention · No Placebo Group · N/A

Experimental (High-Stress) Arm
Behavioral
Experimental Group · 1 Intervention: High-Stress Intervention · Intervention Types: Behavioral
Control ArmNoIntervention Group · 1 Intervention: Control Arm · Intervention Types:

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: hyperpalatable food intake will be measured immediately after the intervention.

Who is running the clinical trial?

University of California, Los AngelesLead Sponsor
1,411 Previous Clinical Trials
6,941,189 Total Patients Enrolled
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)NIH
2,141 Previous Clinical Trials
4,064,075 Total Patients Enrolled
2 Trials studying Food Insecurity
710 Patients Enrolled for Food Insecurity
A. Janet Tomiyama, Ph.D.Principal InvestigatorUniversity of California, Los Angeles
2 Previous Clinical Trials
401 Total Patients Enrolled

Eligibility Criteria

Age 18+ · All Participants · 2 Total Inclusion Criteria

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