- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04968496
Biobehavioral Mechanisms of Food Insecurity
January 24, 2023 updated by: The Miriam Hospital
Isolating Food Insecurity to Understand Childhood Health Outcomes and Biological Mechanisms of Risk
Food insecurity is prevalent in the United States.
Defined as unstable and inadequate access to food, food insecurity disproportionately affects low-income households, those with children and those with a Black or Hispanic head of household.
Moreover, food insecurity is associated with childhood obesity, a relationship that is not well understood from a behavioral or biological perspective.
This randomized controlled trial will take advantage of the natural onset of summertime food insecurity among school-age children, ages 8-12 years, to examine the biobehavioral mechanisms of food insecurity including diet quality, biomarkers of Metabolic Syndrome, inflammation, and stress, weight status, and measures of child mental health.
Study Overview
Status
Terminated
Intervention / Treatment
Detailed Description
Food insecurity affects one in six households with children in the United States and disproportionately impacts those headed by women and minorities.
Food insecurity is associated with childhood obesity, asthma, anxiety and depression and behavioral problems, and thus contributes to health disparities.
While food insecurity likely contributes to poor health through its effect on diet, such a simplistic understanding likely obscures the effects of stress - those unique to childhood, such as Adverse Childhood Experiences including maternal depression, as well as those generally associated with the experience of poverty.
To inform the mechanisms by which food insecurity ultimately affects physical and mental health outcomes in children, this study will disentangle the effects of food insecurity from those of poverty and examine effects on diet, biomarkers, weight gain, mood and behavior while considering other childhood adversities.
Specifically, through a unique summertime meal provision intervention, the proposed project will isolate the experience of food insecurity in children, ages 8 to12 years, from low-income households in Providence, RI.
In partnership with the YMCA of Greater Providence and the Healthy Communities Office in Providence, we will recruit 100 children over two summers.
After completing a baseline assessment, participants will be randomized to receive home-delivered meals throughout the summer or to receive a weekly newsletter.
Children randomized to the newsletter group will experience the natural onset of summertime food insecurity and receive a weekly newsletter on community resources that is not expected to affect food insecurity (Food Insecure Group).
Those randomized to receive meals will remain food secure over the summer through receipt of weekly shipments of five breakfast and lunch meals that meet the nutrition needs of this age group (Food Secure Group).
Primary endpoints include diet quality, biomarkers of Metabolic Syndrome, inflammation, and stress, BMI z-scores, and child measures of behavior and anxiety and depression symptoms.
The impact of caregiver mood and stress on the health effects of food insecurity will also be explored.
Ultimately, findings from this research will clarify the mechanisms by which food insecurity affects child health outcomes and inform how to more effectively prevent food insecurity.
Study Type
Interventional
Enrollment (Actual)
9
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Rhode Island
-
Newport, Rhode Island, United States, 02840
- Newport Housing Authority
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
8 years to 12 years (Child)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- ability of parent and child to speak, read and write English or Spanish
- agreement to study participation and random assignment.
Exclusion Criteria:
- Children will not be eligible if they are enrolled in a full-time camp, day care or programming in which regular meals are provided for more than one-week over the summer.
- Children will not be eligible if their Parent / caregiver does not have reliable phone access to complete study measures.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Food Insecure Group
Children randomized to the naturally-occurring Food Insecure group will receive a weekly newsletter with information on available area-specific food programs.
The weekly newsletter will be sent in two ways: 1) a paper copy will be mailed and 2) a link to an electronic version will be sent via Ilumivu to families to remove any barriers to engagement with the information.
In the absence of school meal programs, children from low-income households are at increased risk for food insecurity during the summer.37-39
Given low engagement in summer food programs, it is not expected that this newsletter will impact food security in this group.
|
|
|
Experimental: Food Secure Group
Children randomized to the Food Secure group will receive breakfast and lunch meals for eight weeks throughout the summer.
Weekly meals will be delivered to each participant's home by Yumble, a company that prepares meals for children ages 3 to 12 years and ships them fresh in insulated, food safe packaging to the home.
The meals have similar nutrition standards to those offered via the National School Lunch Program and include fruits, vegetables, whole grains, and lean/ vegetarian proteins.
To accommodate cultural preferences or dietary constraints, Yumble offers 20 different breakfast, lunch and dinner meals each week.
Families will choose their weekly menus to improve adherence.
Participants who have siblings in their home will be provided a family meal kit, which provides 24 meals each week.
Additional meals will help to prevent household food insecurity and ensure that the child enrolled in the study consumes the meals each week.
|
Weekly meals (five breakfast and five lunch meals) will be provided to all children randomized to this group to prevent the onset of summertime food insecurity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Dietary Quality
Time Frame: 2 months
|
Healthy Eating Index (HEI 2015) - scores range from 0 to 100, with 100 representing perfect adherence to the Dietary Guidelines for Americans, 2015
|
2 months
|
|
Markers of Inflammation
Time Frame: 3 months
|
Blood sample analyzed for C-reactive protein
|
3 months
|
|
Markers of Inflammation
Time Frame: 3 months
|
Blood sample analyzed for interleukin-6 levels
|
3 months
|
|
Markers of Metabolic Syndrome
Time Frame: 3 months
|
Blood sample analyzed for glucose
|
3 months
|
|
Markers of Metabolic Syndrome
Time Frame: 3 months
|
Blood sample analyzed for hemoglobin A1c
|
3 months
|
|
Markers of Metabolic Syndrome
Time Frame: 3 months
|
Blood sample analyzed for insulin
|
3 months
|
|
Markers of Stress
Time Frame: 3 months
|
Blood sample analyzed for cortisol
|
3 months
|
|
Markers of Stress
Time Frame: 3 months
|
Blood sample analyzed for leptin
|
3 months
|
|
Markers of Stress
Time Frame: 3 months
|
Blood sample analyzed for adiponectin
|
3 months
|
|
Child Mood
Time Frame: 3 months
|
PROMIS (Patient-Reported Outcomes Measurement Information System) short-form measures for assessing anxiety in children.
Scores range from 10 to 50 with a higher score indicating greater anxiety symptoms.
|
3 months
|
|
Child Mood
Time Frame: 3 months
|
PROMIS (Patient-Reported Outcomes Measurement Information System) short-form measures for assessing depression in children.
Scores range from 0 to 32 with a higher score indicating greater depressive symptoms.
|
3 months
|
|
Child weight status
Time Frame: 3 months
|
Body Mass Index z-score (BMIz) - Z-score will be determined based on child's BMIz for age and sex using the CDC growth charts
|
3 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 24, 2022
Primary Completion (Actual)
August 26, 2022
Study Completion (Actual)
January 24, 2023
Study Registration Dates
First Submitted
June 15, 2021
First Submitted That Met QC Criteria
July 8, 2021
First Posted (Actual)
July 20, 2021
Study Record Updates
Last Update Posted (Actual)
January 26, 2023
Last Update Submitted That Met QC Criteria
January 24, 2023
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1773080
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Inflammation
-
University of EdinburghUmeå UniversityCompletedSystemic Inflammation | Respiratory InflammationSweden
-
University of AarhusAarhus University Hospital; University of CopenhagenCompletedSystemic Inflammation | Airway InflammationDenmark
-
Sykehuset TelemarkRikshospitalet University Hospital; Helse Sor-OstCompletedAirway Inflammation | Peripheral Blood Inflammation Markers | Cement Dust ExposureNorway
-
Center for Research and Innovation Viña Concha...Universidad Católica del MauleNot yet recruitingInflammaging | Antioxidant Status, Inflammation | Inflammation Biomarkers | Antioxidant Capabilities | Cardiometabolic Health IndicatorsChile
-
University of NebraskaNot yet recruiting
-
Central Hospital, Nancy, FranceRecruiting
-
Oral Science International Inc.AdvarraNot yet recruiting
-
University of NebraskaCompletedPeriodontal InflammationUnited States
-
University of California, DavisCompleted
-
Università degli Studi di BresciaCompletedVitreous Inflammation
Clinical Trials on Food Secure Group
-
Purdue UniversityEnrolling by invitationDiet, Healthy | Hunger | Healthy Eating | Nutrition Intervention | Food SecurityUnited States
-
Wake Forest University Health SciencesNational Institute of Nursing Research (NINR); University of North Carolina...RecruitingPreDiabetes | HIV | Type 2 Diabetes Mellitus (T2DM) | Food Insecurities | Cardiometabolic ComorbiditiesUnited States
-
David Haines, MDTerminatedBradycardia | Atrioventricular Block | Sinus Node DysfunctionUnited States
-
University of PennsylvaniaWithdrawnDiabetes | Renal Failure | Copd | Congestive Heart FailureUnited States
-
Kaiser PermanenteCompletedHypertensionUnited States
-
VA Office of Research and DevelopmentCompleted
-
Miami VA Healthcare SystemPfizerCompleted
-
Universidad Complutense de MadridCompletedXerosis Cutis | Neuropathic Pain Associated With Diabetic Peripheral NeuropathySpain
-
Istanbul University - CerrahpasaThe Scientific and Technological Research Council of TurkeyCompleted
-
Linyi People's HospitalCompletedAtrioventricular Block | Left Bundle Branch PacingChina