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Completed

NCT Number: NCT04652596

Reducing Food Insecurity During COVID-19

This study aims to compare the effectiveness of two interventions to address food insecurity among low-income families with young children during the COVID pandemic. The investigators will conduct a parallel group, randomized controlled trial of 250 families. The first randomly assigned comparator is Fresh Connect, a produce prescription program that provides a stipend for participants to purchase fresh food items at mobile markets and independent farmers markets across Boston. The second comparator is grocery store gift cards, redeemable at conventional grocery stores. In each comparator, participants will be given the equivalent of $150 on a monthly basis for six consecutive months. All participants will be followed for 12 months to assess outcomes that involve food insecurity (primary), fruit and vegetable consumption, healthcare utilization, social service utilization, and physical/emotional health.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Boston Medical Center

Boston, Massachusetts, 02118, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Parent of a child 0-18 months of age
  • Child receives care at Boston Medical Center

Exclusion criteria

  • Planning to move residence outside of Boston within 12 months

Treatment and study plan

Produce prescription program

Other

A monthly $150 stipend will be provided to participants for 6 consecutive months to purchase fresh food items at mobile markets and independent farmers markets across Boston.

Other names: Fresh Connect

Grocery store gift cards

Other

A monthly value of $150 in grocery store gift cards redeemable at conventional grocery stores will be provided to participants for 6 consecutive months.

Primary outcomes

  1. Change in Food Security

    Time frame: Baseline, monthly for 12-months post-enrollment

    Self-reported food security status measured by USDA validated 18-question food insecurity screening tool with a 30-day lookback period. Responses are scored with total scores corresponding to four categories: high food security, marginal food security, low food security, and very low food security

Secondary outcomes

  1. Change in fruit & vegetable consumption

    Time frame: Baseline, monthly for 12 months post-enrollment

    Self-reported consumption frequency of fruits, fruit juices, and vegetables in the past 30 days measured by 10-item Dietary Screener Questionnaire scale. Each item is scored from "never" to "6 or more times per day". Scoring algorithms convert frequency responses to cup equivalent estimates of average daily dietary intake for fruits and vegetables, using an age and gender coefficient. The higher the score the more daily dietary intake for fruits and vegetables.

  2. Depression Symptoms

    Time frame: Baseline, monthly for 12-months post-enrollment

    Assessed by the Quick Inventory of Depressive Symptoms (QIDS SR-16). This scale is a 16-item self-report measure of depressive symptoms over the past 7 days. Each item is scored 0-3 (0 = no presence of the symptom; 3 = high burden of the symptom), yielding a total score range of 0 to 27. Because of its wide scoring range, the QIDS can be used to detect depressive illness in populations with low symptoms. Lower scores reflect less depressive symptoms.

  3. Symptom Relief

    Time frame: Baseline, monthly for 12-months post-enrollment

    Assessed by the Beck Anxiety Inventory (BAI). This scale is a 21-item self-report measure the severity of self-reported anxiety. Each item is scored 0-3 (0 = not at all; 3 = severely - it bothered me a lot), yielding a total score range of 0 to 63. The lower the score the less self-reported anxiety.

  4. Changes of behavioral activation for depression

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by the Behavioral Activation for Depression Scale (BADS). This 25-item self-reported measure is used to track changes weekly in the behaviors hypothesized to underlie depression and specifically targeted for change by behavioral activation. The BADS subscales include activation, avoidance/rumination, work/school impairment, and social impairment. Each item is scored 0-6 (0=not at all; 6=completely), yielding a total score range of 0 to 150. High scores indicate greater levels of activation. For all the subscores, high scores are consistent with the subscale name.

  5. Perceived Stress

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by Perceived Stress Scale (PSS). This 14-item psychological instrument measures the perception of stress and the degree to which situations in one's life are appraised as stressful. Each item is scored 0-4 (0=never; 4= very often). The scores is obtained by first reversing the scores on items 4, 5, 6, 7, 9, 10, and 13 and then summing the reverse coded items with the rest of the items. The scores can range from 0 to 40 with higher scores indicating higher perceived stress.

  6. Social Support

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by Social Adjustment Scale Self-Report (SAS-SR). This 54-item measure examines social and role functioning in six areas: work; social activities; relationships with family; spouse or partner; parent; member of family unit. Items are rated on a 5-point scale. Seven mean scores are generated, six-role areas and one overall means. The mean scores are converted into standard T-scores on the SAS-SR Profile Form. Higher scores indicate greater impairment of functioning.

  7. Medical outcomes social support

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by Medical Outcomes Survey Social Support (MOSSS). This 18-item tool comprises 4 functional support scales (emotional/informational, tangible, affectionate, and positive interaction) and an overall social support index. Each item is scored 0-5 (0=none of the time; 5=all of the time). The higher the overall social support index the more support.

  8. Mastery Control

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by Pearlin Mastery Scale (PMS). This 7-item tool measures the extent to which an individual regards their life chances as being under their personal control rather than fatalistically ruled. Each item is scored 1-4 (1=strongly agree; 4=strongly disagree) and the values are added. The scores can range from 7 to 28 with higher scores reflect greater mastery.

  9. Self-Esteem

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by Rosenberg's Self-Esteem Scale (RSES). This 10-item self-report likert scale evaluates an individual's self-esteem. Each item is scored from strong agree to strongly disagree. The higher the sum of the scores, the higher the self-esteem.

  10. Unmet needs

    Time frame: Baseline, every 3 months during 12 month post-enrollment

    Assessed by WE CARE. This 12-question screening tool assesses needs in 6 domains: parental educational attainment, employment, child care, risk of homelessness, food security, and household heat and electricity. Individuals respond with "Yes", "No", or "Maybe later". Those with unmet needs are provided with a locally developed community resource information sheet.

  11. Self-Reported Food Assistance Program Participation

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Self-reported participation in food assistance programs including Electronic Benefits Transfer (EBT), Food Stamps/Supplemental Nutrition Assistance Program (SNAP).

  12. Change in Self-Reported Health Status

    Time frame: Baseline, monthly for 12-months post-enrollment

    Self-reported health status measured by a report of health status as excellent, very good, good, fair, or poor and measured by 3-item CDC Healthy Days module for a disarticulation of physical and mental health.

  13. Maternal attitudes and safe infant care practices

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Assessed by the Pregnancy Risk Assessment Monitoring System (PRAMS). The survey Identifies groups of women and infants at high risk for health problems, monitors changes in health status, and measures progress towards goals in improving the health of mothers and infants.

  14. Impact of COVID-19

    Time frame: Baseline, every 3 months during 12 month post-enrollment

    The Epidemic - Pandemic Impacts Inventory (EPII) + 4-item self-report of the impact of the pandemic on financial capacity and food purchasing/acquisition patterns. The EPII is newly developed, thus, scoring procedures will be determined by future research.

  15. Program Experience

    Time frame: 6 months post-enrollment, 12 months post-enrollment

    Assessed by 4-item USDA program experience questions. The questions ask about firm type use, dose of program usage, health education, and program satisfaction.

  16. Change in adult acute healthcare utilization

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Claims data composite measure (all cause hospital admissions and ED visits; Total number of all-cause ED visits; Total number of all-cause discharges from IP).

  17. Total adult patient-level cost of care

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    Measured via claims data

  18. Child healthcare utilization

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    EPIC chart abstractions (number of office visits, hospitalizations, missed appointments, immunization rates)

  19. Child weight

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    EPIC chart abstractions (weight for age)

  20. Child height

    Time frame: Baseline, every 6 months during 12 month post-enrollment

    EPIC chart abstractions (height for age)

Sponsors and collaborators

Lead sponsor

Boston Medical Center

Other

Collaborators

  • Krupp Family Foundation
  • Patient-Centered Outcomes Research Institute
  • United States Department of Agriculture (USDA)
  • Waldron Charitable Fund

Registry information

Official study title

Comparative Effectiveness of Two Interventions to Reduce Food Insecurity During the COVID-19 Pandemic

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Dec 3, 2020
Registry last updated
Apr 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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