Stress Management for Food Insecurity
Trial Summary
What is the purpose of this trial?
This study will use a within-subjects design in a sample of individuals with a range of food insecurity recruited from the Los Angeles community (N = 400; 50% men). These participants will then, in counterbalanced order, be exposed to a gold-standard laboratory stressor and a control condition, one month apart. Moderation analyses will test whether cortisol reactivity to the stressor acts as a modulator of the relationship between high levels of food insecurity and increased hyperpalatable food intake.
Do I need to stop taking my current medications for the trial?
The trial does not specify if you need to stop taking your current medications, but it excludes those with recent diagnoses of certain disorders or those using steroids or hormonal contraceptives.
What data supports the effectiveness of the High-Stress Intervention treatment for managing food insecurity?
The study on self-efficacy and food security in a food pantry program shows that interventions focusing on self-efficacy (belief in one's ability to succeed) and motivational interviewing can improve food security. This suggests that stress management techniques, which often enhance self-efficacy, could be effective in addressing food insecurity.12345
How does the stress management treatment for food insecurity differ from other treatments?
This treatment is unique because it focuses on managing stress specifically related to food insecurity, which is often linked to mental health issues like anxiety and depression. Unlike other treatments that might address food insecurity through direct food aid, this approach aims to alleviate the stress caused by the lack of food, potentially improving mental health outcomes.678910
Research Team
A. Janet Tomiyama, Ph.D.
Principal Investigator
University of California, Los Angeles
Eligibility Criteria
This trial is for English-speaking adults over the age of 18 living in Los Angeles who experience varying levels of food insecurity. It's not suitable for those on strict diets, with recent metabolic or psychiatric diagnoses, pregnant women, individuals allergic to foods provided during the study, or those diagnosed with an eating disorder within the last year.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Experimental (High-Stress) Arm
Participants are exposed to a gold-standard laboratory stressor, the Trier Social Stress Test, involving a speech task and a mental arithmetic task
Control Arm
Participants undergo low-stress equivalents to the speech and mental arithmetic tasks from the experimental arm
Follow-up
Participants are monitored for hyperpalatable food intake immediately after the intervention
Treatment Details
Interventions
- High-Stress Intervention
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of California, Los Angeles
Lead Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Collaborator