No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
300 (estimated)
Sponsor
University of Massachusetts, Worcester · Other
Who this trial is looking for
This trial is looking for adults with depression and food insecurity. Participants will receive grocery boxes designed for their health needs every two weeks for six months, along with optional nutritional support.
Are You a Good Fit for This Trial?
You may be able to join if
I have active symptoms of depression.
I experience food insecurity.
I live in Central Massachusetts in Worcester County.
I receive care at UMass Memorial Health or clinics associated with C3.
I can prepare and cook meals independently or have help to do so.
You may not be able to join if
I am pregnant or have had a baby in the past year.
I have been diagnosed with depression in the last 3 months.
I have bipolar depression or bipolar disorder.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
This randomized controlled trial will test whether providing medically tailored groceries for 6 months can improve depressive symptoms among adults with depression and food insecurity.
The intervention under study is a 6-month, medically tailored grocery program provided by the Boston-based non-profit organization, Community Servings. Food boxes are mailed to participants' homes every two weeks a…
This randomized controlled trial will test whether providing medically tailored groceries for 6 months can improve depressive symptoms among adults with depression and food insecurity.
The intervention under study is a 6-month, medically tailored grocery program provided by the Boston-based non-profit organization, Community Servings. Food boxes are mailed to participants' homes every two weeks and are designed by a registered dietitian nutritionists to support an individuals' health needs. Participants may also attend optional nutritional counseling sessions.
In this randomized clinical trial, 300 adults with depression and food insecurity will be assigned to one of two groups. The intervention group will receive medically tailored grocery boxes delivered to their home every two weeks for six months (13 boxes total), along with nutritional counseling support. The comparison group will receive usual medical care plus a $30 monthly grocery gift card for six months to be used to purchase any products of their choice.
Participants will be recruited from UMass Memorial Health and health centers associated with Community Care Cooperative (C3) in the greater Worcester area in Massachusetts.The main goal of the study is to determine whether the grocery program reduces symptoms of depression. The study will also examine effects on anxiety, food insecurity, diet quality, and healthcare use.
Trial Locations
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Status
Eligibility Criteria
Inclusion Criteria:
* A depression diagnosis with active symptoms, defined as having a recent Patient Health Questionnaire (PHQ-9) screening of 5+, or no depression diagnosis but a recent PHQ-9 screening of 10+
* Experiencing food insecurity (could be either low or very low food security)
* Lives i…
Inclusion Criteria:
* A depression diagnosis with active symptoms, defined as having a recent Patient Health Questionnaire (PHQ-9) screening of 5+, or no depression diagnosis but a recent PHQ-9 screening of 10+
* Experiencing food insecurity (could be either low or very low food security)
* Lives in Central Massachusetts in Worcester County
* Receives care at UMass Memorial Health, or receives care at clinics affiliated with Community Care Cooperative (C3)
* Can prepare and cook meals independently, or has a family member or caregiver able to prepare food
Exclusion Criteria:
* Pregnant women and women who are within one year postpartum at baseline. Women who become pregnant during trial will be allowed to finish their food programming and study participation.
* New depression diagnosis within the past 3 months
* Has bipolar depression or bipolar disorder
* Expresses suicide ideation in baseline depression screening defined as responding "nearly everyday" to question #9 in the Patient Health Questionnaire: "Over the last 2 weeks, how often have you been bothered by any of the following problems - Thoughts that you would be better off dead, or of hurting yourself?"
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