Impact of BC Farmers' Market Nutrition Coupon Program on Diet Quality and Psychosocial Well-being of Low-income Adults

February 27, 2023 updated by: University of Calgary

Impact of a Farmers' Market Nutrition Coupon Program on Diet Quality and Psychosocial Well-being Among Low-income Adults: A Randomized Controlled Trial

The British Columbia (BC) Farmers' Market Nutrition Coupon Program (FMNCP) provides low-income households with $21/week in coupons to purchase healthy foods at farmers' markets and supportive nutrition skill-building activities. This randomized controlled trial will assess the impact of the BC FMNCP on the overall diet quality (primary outcome), diet quality subscores, mental well-being, sense of community, experiences of food insecurity, risk of malnutrition (secondary outcomes) and subjective social status (exploratory outcome) of low-income adults immediately post-intervention and 16 weeks post-intervention.

Study Overview

Detailed Description

Background: The British Columbia (BC) Farmers' Market Nutrition Coupon Program (FMNCP) is a healthy eating initiative funded by the BC Ministry of Health. The program provides low-income households with $21/week in coupons to purchase healthy foods at farmers' markets and supportive nutrition skill-building activities. It is not clear if the BC FMNCP is achieving its aims of improving the diet quality, well-being and health of low-income adults, as its outcomes have not been investigated, and studies of similar programs are limited by weak designs that cannot demonstrate causality. This randomized controlled trial will assess the impact of the FMNCP on the overall diet quality (primary outcome), diet quality subscores, mental well-being, sense of community, experiences of food insecurity, risk of malnutrition (secondary outcomes) and subjective social status (exploratory outcome) of low-income adults immediately post-intervention and 16 weeks post-intervention. A qualitative investigation will also explore mechanisms of action and strategies to maximize positive program impacts.

Methods: Low-income adults (≥ 18 years) from up to 15 rural and urban communities will be randomized to a FMNCP intervention (n=132) or a no-intervention control group (n=132), with a 1:1 allocation ratio. An independent researcher from the Clinical Research Unit at the University of Calgary will generate a blocked randomization sequence that stratifies participants into blocks according to sex (male, female), geographic location (rural, urban), pregnancy (yes, no) and breastfeeding (yes, no). In the existing BC FMNCP, community partners distribute one to two sheets of coupons per week (each sheet contains $21 in coupons) to program participants for a total of 16 sheets. Coupons can be used over 16-20 weeks to purchase fruits, vegetables, dairy, meat/poultry/fish, eggs, nuts, and cut herbs at participating BC farmers' markets. However, to allow sufficient time to recruit participants for this study, community partners will distribute 16 coupon sheets to the FMNCP group over 10-15 weeks (households with 5-8 individuals will receive 32 coupon sheets). To ensure participants receive all 16 coupon sheets, community partners will provide two coupon sheets per household during the first 1-6 weeks of the intervention. Participants in the FMNCP group will also be invited to participate in nutrition skill-building activities (e.g., cooking classes). At baseline (0 weeks), immediately post-intervention (10-15 weeks) and 16 weeks post-intervention (26-31 weeks), participants will access a pilot-tested web-based platform to report sociodemographics, health-related variables, mental well-being, sense of community, experiences of food insecurity, risk of malnutrition and subjective social status. Dietary intake will be assessed via two 24-hour dietary recalls at each time point using the Automated Self-Administered Dietary Assessment Tool for Canada (ASA24-Canada-2018). Diet quality scores will be calculated using the Healthy Eating Index-2015. In addition, immediately post-intervention only, participants will report whether they received FMNCP coupons and attended nutrition skill-building activities (to assess contamination of the control group), how often and how much of their own money was spent at farmers' markets during the intervention period and the types of foods purchased.

Data analysis: Descriptive analyses will be conducted to examine participant characteristics by group at each time point. Characteristics of study completers (i.e., provided data 16-weeks post-intervention) and non-completers will also be compared.

Analyses will be intention-to-treat, in which participants will be analysed within the groups to which they were randomized regardless of adherence (e.g., failure to redeem coupons) or dropout. The analyses will include all participants who provided data at baseline. Repeated measures mixed-effect regression will assess differences in mean HEI-2015 scores, HEI-2015 subscores, mental well-being, sense of community, and subjective social status between the FMNCP and control groups immediately post-intervention and 16-weeks post-intervention. Repeated measures multinomial logistic regression will be used to assess differences in the odds of experiencing household food insecurity and risk of malnutrition for the FMNCP group compared to the control group immediately post-intervention and 16-weeks post-intervention. Statistical models will include intervention group (FMNCP vs control), time from baseline, intervention-by-time interaction, blocking variables (i.e., sex, rural/urban, pregnancy, breastfeeding), baseline values of the outcome, and household size as fixed effects covariates. Participant-specific (i.e., repeated measures) variations in outcomes will be modeled using random effects. Models will also include covariates specific to each outcome to increase the precision of estimates (86). For the primary outcome of overall diet quality, models will include the following: children living in the home (yes, no), sex, age, BMI, marital status, race/ethnicity, perceived health, smoking, day of data collection, and educational level. Adjusted group differences (i.e., FMNCP group vs control group) in outcomes will be estimated using 95% confidence intervals and corresponding p-values.

Subgroup analyses will examine whether the impact of the intervention on primary and secondary outcomes differs according to age group or sex. Dose-response analyses will examine whether the impact of the BC FMNCP on overall diet quality depends on the number of coupons redeemed and the number of nutrition skill-building activities attended. Interactions will be retained in statistical models if p<0.10. Analyses will be conducted in Stata (v15.1, Stata Corp, TX, USA), with p<0.05 indicating statistically significant differences between groups. Data interpretation will jointly consider effect sizes, confidence intervals and statistical significance.

Expected outcomes: Findings will show whether and how a scalable population-level policy that links the agricultural and health sectors influences diet quality, psychosocial well-being and other outcomes among low-income adults. Study findings will inform program adjustments to improve participant outcomes. Other jurisdictions can use these data to determine whether and how to initiate similar programs.

Post-hoc analysis: In a post-hoc analysis, a random forest model will be used to explore heterogeneity of program effects on diet quality (total HEI-2015 scores) among different subgroups of FMNCP study participants. Candidate predictors entered into the algorithm will include all variables examined at baseline, including sociodemographic characteristics (e.g., age, sex, and income) and health-related variables (e.g., self-rated health and smoking). The outcome of the random forest analysis will be total HEI-2015 scores for both the FMNCP and control groups.

Study Type

Interventional

Enrollment (Actual)

264

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

    • British Columbia
      • Rural And Urban, British Columbia, Canada
        • Community Partners

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Individuals will be eligible to participate if they meet the following criteria:

  • Adults (age ≥ 18 years)
  • Low-income as determined by community-specific thresholds (~$18,000/year annual household income before taxes)
  • No expected change in household income prior to study completion (March 2020)
  • 8 or fewer people living in the home (including the participant)
  • No expected change in household composition prior to study completion (March 2020)
  • Primary food shopper for the household
  • Does not have self-reported dementia or Alzheimer's Disease
  • Able to speak, read and write in English (or have someone who can assist them)
  • No plans to move from principal residence prior to study completion (March 2020)
  • Has not previously participated in the BC FMNCP

Exclusion Criteria:

• Does not meet one or more inclusion criteria

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: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Nutrition Coupons
Participants in the FMNCP group will receive 16 coupon sheets (each sheet contains $21 in coupons) over 10-15 weeks (households with 5-8 individuals will receive 32 coupon sheets) to purchase fruits, vegetables, dairy, meat/poultry/fish, eggs, nuts, and cut herbs at participating BC farmers' markets. To ensure participants receive all 16 coupon sheets, community partners will provide two coupon sheets per household during the first 1-6 weeks of the intervention. Participants in the FMNCP group will also be invited to participate in nutrition skill-building activities (e.g., cooking classes) offered by community partners throughout the intervention period, however participation is not required (this is consistent with the existing FMNCP).
Participants will receive 16 coupon sheets (each sheet contains $21 in coupons) over 10-15 weeks (households with 5-8 individuals will receive 32 coupon sheets) to purchase fruits, vegetables, dairy, meat/poultry/fish, eggs, nuts, and cut herbs at participating BC farmers' markets.
Participants will be invited to participate in nutrition skill-building activities throughout the intervention period. To be consistent with the real-world program, the frequency and types of skill-building activities offered will vary by community partner, and participation is not required.
No Intervention: Control
No intervention provided. Participants will be eligible to participate in the BC Farmers' Market Nutrition Coupon Program during the next farmers' market season (i.e. one year following the current intervention).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference between intervention and control groups in mean overall diet quality by Healthy Eating Index-2015 scores immediately post-intervention (10-15 weeks)
Time Frame: Assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls and can range from 0-100, with a higher score indicating higher diet quality.
Assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in mean overall diet quality by Healthy Eating Index-2015 scores at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls and can range from 0-100, with a higher score indicating higher diet quality.
Assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference between intervention and control groups in mean mental well-being scores by Warwick-Edinburgh Mental Well-Being Scale immediately post-intervention (10-15 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Items on the 14-item Warwick-Edinburgh Mental Well-Being Scale are self-reported over the past two weeks. There are 14 items with 5 response categories (1=none of the time; 5=all of the time), summed to provide a single score ranging from 14-70. A higher score indicates higher perceived mental well-being.
Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in mean mental well-being scores by Warwick-Edinburgh Mental Well-Being Scale at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Items on the 14-item Warwick-Edinburgh Mental Well-Being Scale are self-reported over the past two weeks. There are 14 items with 5 response categories (1=none of the time; 5=all of the time), summed to provide a single score ranging from 14-70. A higher score indicates higher perceived mental well-being.
Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Difference between intervention and control groups in mean sense of community by the Brief Sense of Community scale immediately post-intervention (10-15 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Items on the 8-item Brief Sense of Community Scale are self-reported in which each item is scored using a Likert Scale of 1 (strongly disagree) to 5 (strongly agree). Scores can range from 8-40. A higher score indicates a stronger sense of community.
Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in mean sense of community by the Brief Sense of Community scale at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Items on the 8-item Brief Sense of Community Scale are self-reported in which each item is scored using a Likert Scale of 1 (strongly disagree) to 5 (strongly agree). Scores can range from 8-40. A higher score indicates a stronger sense of community.
Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Difference between intervention and control groups in the odds of experiencing household food insecurity immediately post-intervention (10-15 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Items on the 18-item Household Food Security Survey Module are self-reported in relation to experiences in the past month.
Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in the odds of experiencing household food insecurity at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Items on the 18-item Household Food Security Survey Module are self-reported in relation to experiences in the past month.
Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Difference between intervention and control groups in the odds of malnutrition by Malnutrition Universal Screening Tool immediately post-intervention (10-15 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Items on the Malnutrition Universal Screening Tool are self-reported and based on BMI (scored as 0= >20, 1= 18.5-20, 2 = <18.5) and percent of unplanned weight loss in the past 3-4 months (scored as 0 = <5%, 1 = 5-10%, 2 = >10%). Overall risk of malnutrition will be scored as 0=low risk, 1= medium risk, and >= 2= high risk.
Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in the odds of malnutrition by Malnutrition Universal Screening Tool at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Items on the Malnutrition Universal Screening Tool are self-reported and based on BMI (scored as 0= >20, 1= 18.5-20, 2 = <18.5) and percent of unplanned weight loss in the past 3-4 months (scored as 0 = <5%, 1 = 5-10%, 2 = >10%). Overall risk of malnutrition will be scored as 0=low risk, 1= medium risk, and >= 2= high risk.
Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Difference between intervention and control groups in mean diet quality subscores by Healthy Eating Index-2015 immediately post-intervention (10-15 weeks)
Time Frame: Assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls. Subscores include adequacy (total fruits, whole fruits, total vegetables, greens and beans, whole grains, dairy, total protein foods, seafood and plant proteins, fatty acids) and moderation components (refined grains, sodium, added sugars, saturated fats), each of which are scored from 0-5 or 0-10.
Assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in mean diet quality subscores by Healthy Eating Index-2015 at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls. Subscores include adequacy (total fruits, whole fruits, total vegetables, greens and beans, whole grains, dairy, total protein foods, seafood and plant proteins, fatty acids) and moderation components (refined grains, sodium, added sugars, saturated fats), each of which are scored from 0-5 or 0-10.
Assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Difference between intervention and control groups in mean subjective social status by the MacArthur Scale of Subjective Social Status community ladder immediately post-intervention (10-15 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
The MacArthur Scale of Subjective Social Status community ladder consists of a self-reported visual analog scale, whereby respondents place themselves on a ladder rung according to their perceived social standing relative to others in their community. Responses can take a value from 1-10, with a higher score indicating higher perceived social status in relation to others' within ones' community.
Assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Difference between intervention and control groups in mean subjective social status by the MacArthur Scale of Subjective Social Status community ladder at 16 weeks post-intervention (26-31 weeks)
Time Frame: Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks)
The MacArthur Scale of Subjective Social Status community ladder consists of a self-reported visual analog scale, whereby respondents place themselves on a ladder rung according to their perceived social standing relative to others in their community. Responses can take a value from 1-10, with a higher score indicating higher perceived social status in relation to others' within ones' community.
Assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks)
Dose response for impact of intervention on overall diet quality (by Health Eating Index-2015) by number of food coupons redeemed immediately post-intervention (10-15 weeks)
Time Frame: Coupon redemption assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks). Diet quality assessed twice at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Objective data on number of coupons redeemed (0-112) over 10-15 weeks. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Coupon redemption assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks). Diet quality assessed twice at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Dose response for impact of intervention on overall diet quality (by Health Eating Index-2015) by number of food coupons redeemed at 16 weeks post-intervention (26-31 weeks)
Time Frame: Coupon redemption assessed weekly from baseline (0 weeks) to 16 weeks post-intervention (26-31 weeks). Diet quality assessed twice at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Objective data on number of coupons redeemed (0-112) over 10-15 weeks. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Coupon redemption assessed weekly from baseline (0 weeks) to 16 weeks post-intervention (26-31 weeks). Diet quality assessed twice at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Dose response for impact of intervention on overall diet quality (by Healthy Eating Index-2015) by number of skill-building activities attended immediately post-intervention (10-15 weeks)
Time Frame: Participation in skill-building assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks). Dietary intake assessed twice at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Objective data on number of nutrition skill-building activities attended over 10-15 weeks. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Participation in skill-building assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks). Dietary intake assessed twice at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Dose response for impact of intervention on overall diet quality (by Healthy Eating Index-2015) by number of skill-building activities attended at 16 weeks post-intervention (26-31 weeks)
Time Frame: Participation in skill-building assessed weekly from baseline (0 weeks) to 16 weeks post-intervention (26-31 weeks). Dietary intake assessed twice at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Objective data on number of nutrition skill-building activities attended over 10-15 weeks. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Participation in skill-building assessed weekly from baseline (0 weeks) to 16 weeks post-intervention (26-31 weeks). Dietary intake assessed twice at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Subgroup analysis for impact of intervention on overall diet quality (assessed by Healthy Eating Index-2015) by sex immediately post-intervention (10-15 weeks)
Time Frame: Sex assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Self-reported sex (male, female). Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Sex assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Subgroup analysis for impact of intervention on overall diet quality (assessed by Healthy Eating Index-2015) by age immediately post-intervention (10-15 weeks)
Time Frame: Age assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Self-reported age. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Age assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Subgroup analysis for impact of intervention on overall diet quality (assessed by Healthy Eating Index-2015) by sex at 16 weeks post-intervention (26-31 weeks)
Time Frame: Sex assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Self-reported sex (male, female). Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Sex assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Subgroup analysis for impact of intervention on overall diet quality (assessed by Healthy Eating Index-2015) by age at 16 weeks post-intervention (26-31 weeks)
Time Frame: Age assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Self-reported age. Healthy Eating Index-2015 scores are calculated from 24-hour dietary recalls.
Age assessed once at baseline. Dietary intake assessed at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Subgroup analysis for impact of intervention on secondary outcomes by sex immediately post-intervention (10-15 weeks)
Time Frame: Sex assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Self-reported sex (male, female).
Sex assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Subgroup analysis for impact of intervention on secondary outcomes by age immediately post-intervention (10-15 weeks)
Time Frame: Age assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Self-reported age.
Age assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and post-intervention (10-15 weeks).
Subgroup analysis for impact of intervention on secondary outcomes by age at 16 weeks post-intervention (26-31 weeks)
Time Frame: Age assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Self-reported age.
Age assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Subgroup analysis for impact of intervention on secondary outcomes by sex at 16 weeks post-intervention (26-31 weeks)
Time Frame: Sex assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Self-reported sex (male, female).
Sex assessed once at baseline. Secondary outcomes assessed once at each of the following time points: Baseline (0 weeks) and 16 weeks post-intervention (26-31 weeks).
Food purchasing at farmers' markets
Time Frame: Assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks)
Self-reported and objective data on food purchasing using coupons and own money (including food type and dollar amount) at farmers' markets
Assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks)
Nutrition skill-building activity attendance
Time Frame: Assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks)
Objective data on attendance to nutrition skill-building activities (including number and types of activities)
Assessed weekly from baseline (0 weeks) to post-intervention (10-15 weeks)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Dana Olstad, PhD, RD, University of Calgary

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 30, 2019

Primary Completion (Actual)

March 31, 2020

Study Completion (Actual)

March 31, 2020

Study Registration Dates

First Submitted

May 10, 2019

First Submitted That Met QC Criteria

May 15, 2019

First Posted (Actual)

May 16, 2019

Study Record Updates

Last Update Posted (Actual)

March 1, 2023

Last Update Submitted That Met QC Criteria

February 27, 2023

Last Verified

June 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • REB18-0508

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.

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