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Healthy Food Prescription Incentive Program

Primary Purpose

Diet, Healthy, Diabetes Mellitus, Type 2, Diabetes Complications

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Healthy food incentive
Healthy food prescription
Sponsored by
University of Calgary
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diet, Healthy

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults (18-85 years) with type 2 diabetes (or diabetes of unknown etiology)
  • Persistent hyperglycemia (i.e. hemoglobin A1C 6.5-12%)
  • Are currently experiencing food insecurity and/or report that it is difficult/very difficult to make ends meet
  • Can communicate in English or have someone to translate

Exclusion Criteria:

  • A1c <6.5% or > 12% given the recommendation for anti-hyperglycemic treatment escalation for those with A1c>12%
  • Reside in a facility that provides meals (e.g., shelter, long-term care, prison)
  • Exhibit signs/symptoms of metabolic decompensation (weight loss, polyuria, polydipsia)
  • Diagnosis of eating disorder(s) (e.g., anorexia nervosa, bulimia)
  • Have experienced diabetic ketoacidosis or a hyperglycemic hyperosmolar emergency in the past year
  • Experienced a hypoglycemic event in the past 3 months
  • Are trying to conceive, pregnant and/or breastfeeding
  • Are currently participating in other clinical trials
  • A household member is currently or has previously participated in this trial
  • Unwilling/unable to shop in study-affiliated supermarkets for the next 12 months
  • Plan to leave for Canada for more than 2 weeks in the next 12 months
  • Unable to complete data collection at follow-up (e.g., due to moving)

Sites / Locations

  • Primary Care ClinicsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Subsidized Healthy Food Prescription Incentive

Healthy Food Prescription Comparison

Arm Description

Participants will receive a one-time healthy food prescription pamphlet from their healthcare provider and a weekly incentive of $10.50/household member to purchase healthy foods in supermarkets for 12 months. The list of incentive-eligible foods includes whole, minimally processed foods with little to no added fat, sugar or salt from all food groups.

Participants will receive a one-time healthy food prescription pamphlet from their healthcare provider. The pamphlet closely mimics current standard of care for patients with diabetes in Alberta (i.e., nutrition counselling).

Outcomes

Primary Outcome Measures

Blood glucose levels via hemoglobin A1C
Difference between intervention and comparison groups in blood glucose levels measured by hemoglobin A1C

Secondary Outcome Measures

Blood glucose levels via elevated hemoglobin A1C
Difference between intervention and comparison groups in proportion of patients with elevated hemoglobin A1C (>/=8.5%)
Blood glucose levels via fructosamine
Difference between intervention and comparison groups in blood glucose levels via fructosamine
Overall diet quality by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Difference between intervention and comparison groups in mean diet quality by Healthy Eating Index-2015 scores and by Healthy Eating Food Index-2019 scores
Diet quality sub-scores by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Difference between intervention and comparison groups in diet quality component scores by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Fruit and vegetable intake via skin carotenoids
Difference between intervention and comparison groups in skin carotenoids
Blood Lipids
Difference between intervention and comparison groups in blood lipids including total-, HDL- and LDL-cholesterol, triglycerides, apolipoprotein B
Blood Pressure
Difference between intervention and comparison groups in both systolic and diastolic blood pressure
Body Mass Index
Difference between intervention and comparison groups in Body Mass Index
Waist Circumference
Difference between intervention and comparison groups in waist circumference
Anti-hyperglycemic Medication/Insulin
Difference between intervention and comparison groups in need for anti-hyperglycemic medication and/or insulin.
World Health Organization-5 Well-Being Scale scores
Difference between intervention and comparison groups in World Health Organization Well-Being Scale scores. The World Health Organization Well-Being scale will be used to assess experiences of well-being in the last 2 weeks with scores ranging from 0 (worst possible quality of life) to 25 (best imaginable quality of life).
Stanford Diabetes Self-efficacy Scale scores
Difference between intervention and comparison groups in Stanford Diabetes Self-efficacy Scale scores. The Stanford Diabetes Self-efficacy Scale will be used to assess confidence in completing activities related to diabetes. Scores range from 8 (not confident at all) to 80 (totally confident).
Diabetes Self-Management Questionnaire scores
Difference between intervention and comparison groups in ability to self manage diabetes- related activities. The Diabetes Self-Management Questionnaire will be used to assess effective self-care behaviour, with a score of 0 indicating least effective self-care behaviour and 10 indicating most effective self-care.
Problem Areas in Diabetes Scale scores
Difference between intervention and comparison groups in Diabetes Scale scores. The Problem Areas in Diabetes Scale will assess emotional distress related to diabetes. Scores can range from 0-100, with scores above 40 indicating higher levels of emotional burnout and scores below 10 indicating denial when combined with poor glycemic control.
EQ-5D-5L scores
Difference between intervention and comparison groups in self-reported overall health. The EQ-5D-5L is a 5-item tool that will be used to assess health factors such as mobility, self care, usual activities, pain, anxiety. Level 1 scores indicate "no problems", levels 2-4 scores indicate more frequent problems, level 5 indicates extreme impairments.
Hypoglycemic Episodes
Difference between intervention and comparison groups in frequency of hypoglycemic episodes. Frequency of hypoglycemic episodes is measured using a single question ("In the past year, how many times have you had a severe low blood sugar reaction, such as passing out or needing help to treat the reaction?"). Categorical responses include 0, 1-3, 4-6, 7-11, 12 or more. Severe hypoglycemia is indicated at 4 or more times.
Barriers to Care for People with Chronic Health Conditions scores
Difference between intervention and comparison groups in barriers to care. The Barriers to Care for People with Chronic Health Conditions - Economic Barriers to Care scale and Insurance scale will assess economic related barriers in accessing care, which includes services, equipment, and/or medication. Responses of "always", "often", or "sometimes" indicate economic barriers are present.
Health Canada's Household Food Security Survey Module scores
Difference between intervention and comparison groups in experiences of household food insecurity. Health Canada's 18-item Household Food Security Survey Module will be used to assess experiences of marginal (1 affirmative response), moderate (2-5 affirmative responses) and severe (≥ 6 affirmative responses) household food insecurity in the past 6 months.
Diabetes Competing Demands scores
Difference between intervention and comparison groups in Diabetes Competing Demands scores. The Diabetes Competing Demands 2-item scale will be used to assess the frequency of trade-offs between food, medicine, and diabetes supplies. A response of "often" or "sometimes" to either question indicates trade-offs have occurred.

Full Information

First Posted
January 19, 2021
Last Updated
February 26, 2023
Sponsor
University of Calgary
Collaborators
Alberta Innovates Health Solutions, Alberta Health services, Alberta Blue Cross, Nu Skin, Canadian Institutes of Health Research (CIHR)
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1. Study Identification

Unique Protocol Identification Number
NCT04725630
Brief Title
Healthy Food Prescription Incentive Program
Official Title
A Healthy Food Prescription Incentive Program for Adults With Type 2 Diabetes Who Are Experiencing Food Insecurity
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 29, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Calgary
Collaborators
Alberta Innovates Health Solutions, Alberta Health services, Alberta Blue Cross, Nu Skin, Canadian Institutes of Health Research (CIHR)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
It is important for individuals with type 2 diabetes (T2DM) to adhere to a healthy dietary pattern to maintain optimal blood glucose levels and overall health. The increasing costs of healthy foods, however, is a barrier to maintaining healthful dietary patterns, particularly for individuals with T2DM who are experiencing food insecurity (i.e., inadequate or insecure access to food due to financial constraints). Lower diet quality may result in difficulties maintaining optimal blood glucose levels, leading to higher rates of diabetes complications, and increased acute care usage and costs. Effective strategies to address this issue are lacking despite the well-known impact of food insecurity on maintaining optimal blood glucose levels. One way to address this problem is to provide incentives to purchase healthy foods through healthy food prescription programs. These programs may help to reduce food insecurity and improve diet quality, thereby improving blood glucose control and reducing diabetes complications over time. This study will investigate the reach, effectiveness, adoption, implementation, and maintenance (RE-AIM) of a healthy food prescription incentive program among adults who are experiencing food insecurity and persistent hyperglycemia through three concurrent studies; a randomized controlled trial, an implementation study, and a modelling study. The randomized controlled trial will examine the effectiveness of a healthy food prescription incentive program compared to a healthy food prescription alone in reducing blood glucose levels among adults who are experiencing food insecurity and persistent hyperglycemia.
Detailed Description
It is vital for individuals with type 2 diabetes (T2DM) to adhere to a healthy dietary pattern to maintain optimal blood glucose levels and overall health. However, the increasing costs of healthy foods is a barrier to maintaining healthful dietary patterns, particularly for individuals with T2DM who are experiencing food insecurity (i.e., inadequate or insecure access to food due to financial constraints). Lower diet quality may result in difficulties maintaining optimal blood glucose levels, leading to higher rates of diabetes complications, and increased acute care usage and costs. Although the adverse impact of food insecurity on maintaining optimal blood glucose levels is well documented, effective strategies to address food insecurity among individuals with T2DM are lacking. One approach to address this problem is to provide incentives for individuals to purchase healthy foods through healthy food prescription programs. These programs may help to reduce food insecurity and improve diet quality, thereby improving blood glucose levels and reducing diabetes complications over time. Using a type 2 hybrid effectiveness-implementation design, we will conduct three concurrent studies (i.e. randomized controlled trial, implementation study, modelling study) to examine the reach, effectiveness, adoption, implementation, and maintenance (RE-AIM) of a healthy food prescription incentive program among adults who are experiencing food insecurity and persistent hyperglycemia. The randomized controlled trial will examine the effectiveness of a healthy food prescription incentive program compared to a healthy food prescription alone in improving blood glucose levels, quantified via hemoglobin A1C, among adults who are experiencing food insecurity and persistent hyperglycemia. Secondary outcomes include blood glucose levels quantified via fructosamine, the proportion of patients with elevated hemoglobin A1C (i.e. ≥ 8.5%), diet quality and skin carotenoid levels, intermediate clinical outcomes (blood lipids, blood pressure, BMI, waist circumference, need for anti-hyperglycemic medication/insulin) and patient-reported outcomes (psychosocial well-being, self-rated health, diabetes self-efficacy, diabetes self-management, diabetes distress, diabetes competing demands, perceived financial barriers to chronic disease care, hypoglycemic episodes, household food insecurity). Methods: 594 adults who are experiencing food insecurity and persistent hyperglycemia (i.e., hemoglobin A1C 6.5-12%) from urban and rural primary care clinics will be randomized to a 12 month healthy food prescription incentive (n=297) or a healthy food prescription comparison group (n=297). The healthy food prescription incentive program consists of the following two core elements: 1) The one-time healthy food prescription pamphlet is a low literacy resource comprised of a pre-printed healthy food prescription that outlines an evidence-based healthy dietary pattern; 2) The healthy food incentive provides a weekly incentive of $10.50/household member to purchase healthy foods in participating supermarkets for 12 months. The intervention will be delivered over 12 months to allow sufficient time for dietary changes to be reflected in several A1c cycles. At baseline (0 months) and follow-up (12 months), participants will access a pilot-tested web-based platform to provide responses to sociodemographic and health-related items, and a variety of patient-reported outcomes, including household food insecurity. To assess diet quality, 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). Clinical measurements (biochemical and physical measurements) will be obtained to assess blood glucose, blood lipids, BMI, blood pressure, skin carotenoids, and waist circumference. Need for anti-hyperglycemic medication/insulin will be quantified via administrative health records. At 6 months and 18 months participants will have their blood glucose levels measured. They will also report their dietary intake via two 24-hour dietary recalls and their household food insecurity status.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diet, Healthy, Diabetes Mellitus, Type 2, Diabetes Complications

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
Investigators will be blinded to group allocation during data collection.
Allocation
Randomized
Enrollment
594 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Subsidized Healthy Food Prescription Incentive
Arm Type
Experimental
Arm Description
Participants will receive a one-time healthy food prescription pamphlet from their healthcare provider and a weekly incentive of $10.50/household member to purchase healthy foods in supermarkets for 12 months. The list of incentive-eligible foods includes whole, minimally processed foods with little to no added fat, sugar or salt from all food groups.
Arm Title
Healthy Food Prescription Comparison
Arm Type
Active Comparator
Arm Description
Participants will receive a one-time healthy food prescription pamphlet from their healthcare provider. The pamphlet closely mimics current standard of care for patients with diabetes in Alberta (i.e., nutrition counselling).
Intervention Type
Behavioral
Intervention Name(s)
Healthy food incentive
Intervention Description
$10.50/week/household member for 12 months to purchase healthy foods in participating supermarkets.
Intervention Type
Behavioral
Intervention Name(s)
Healthy food prescription
Intervention Description
A one-time healthy food prescription pamphlet
Primary Outcome Measure Information:
Title
Blood glucose levels via hemoglobin A1C
Description
Difference between intervention and comparison groups in blood glucose levels measured by hemoglobin A1C
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Secondary Outcome Measure Information:
Title
Blood glucose levels via elevated hemoglobin A1C
Description
Difference between intervention and comparison groups in proportion of patients with elevated hemoglobin A1C (>/=8.5%)
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Title
Blood glucose levels via fructosamine
Description
Difference between intervention and comparison groups in blood glucose levels via fructosamine
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Title
Overall diet quality by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Description
Difference between intervention and comparison groups in mean diet quality by Healthy Eating Index-2015 scores and by Healthy Eating Food Index-2019 scores
Time Frame
Assessed twice at Baseline (0 months) and twice at Follow-up (6 months, 12 months, 18 months)
Title
Diet quality sub-scores by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Description
Difference between intervention and comparison groups in diet quality component scores by Healthy Eating Index-2015 and by Healthy Eating Food Index-2019
Time Frame
Assessed twice at Baseline (0 months) and twice at Follow-up (6 months, 12 months, 18 months)
Title
Fruit and vegetable intake via skin carotenoids
Description
Difference between intervention and comparison groups in skin carotenoids
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Blood Lipids
Description
Difference between intervention and comparison groups in blood lipids including total-, HDL- and LDL-cholesterol, triglycerides, apolipoprotein B
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Blood Pressure
Description
Difference between intervention and comparison groups in both systolic and diastolic blood pressure
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Body Mass Index
Description
Difference between intervention and comparison groups in Body Mass Index
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Waist Circumference
Description
Difference between intervention and comparison groups in waist circumference
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Anti-hyperglycemic Medication/Insulin
Description
Difference between intervention and comparison groups in need for anti-hyperglycemic medication and/or insulin.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
World Health Organization-5 Well-Being Scale scores
Description
Difference between intervention and comparison groups in World Health Organization Well-Being Scale scores. The World Health Organization Well-Being scale will be used to assess experiences of well-being in the last 2 weeks with scores ranging from 0 (worst possible quality of life) to 25 (best imaginable quality of life).
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Stanford Diabetes Self-efficacy Scale scores
Description
Difference between intervention and comparison groups in Stanford Diabetes Self-efficacy Scale scores. The Stanford Diabetes Self-efficacy Scale will be used to assess confidence in completing activities related to diabetes. Scores range from 8 (not confident at all) to 80 (totally confident).
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Diabetes Self-Management Questionnaire scores
Description
Difference between intervention and comparison groups in ability to self manage diabetes- related activities. The Diabetes Self-Management Questionnaire will be used to assess effective self-care behaviour, with a score of 0 indicating least effective self-care behaviour and 10 indicating most effective self-care.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Problem Areas in Diabetes Scale scores
Description
Difference between intervention and comparison groups in Diabetes Scale scores. The Problem Areas in Diabetes Scale will assess emotional distress related to diabetes. Scores can range from 0-100, with scores above 40 indicating higher levels of emotional burnout and scores below 10 indicating denial when combined with poor glycemic control.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
EQ-5D-5L scores
Description
Difference between intervention and comparison groups in self-reported overall health. The EQ-5D-5L is a 5-item tool that will be used to assess health factors such as mobility, self care, usual activities, pain, anxiety. Level 1 scores indicate "no problems", levels 2-4 scores indicate more frequent problems, level 5 indicates extreme impairments.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Hypoglycemic Episodes
Description
Difference between intervention and comparison groups in frequency of hypoglycemic episodes. Frequency of hypoglycemic episodes is measured using a single question ("In the past year, how many times have you had a severe low blood sugar reaction, such as passing out or needing help to treat the reaction?"). Categorical responses include 0, 1-3, 4-6, 7-11, 12 or more. Severe hypoglycemia is indicated at 4 or more times.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Barriers to Care for People with Chronic Health Conditions scores
Description
Difference between intervention and comparison groups in barriers to care. The Barriers to Care for People with Chronic Health Conditions - Economic Barriers to Care scale and Insurance scale will assess economic related barriers in accessing care, which includes services, equipment, and/or medication. Responses of "always", "often", or "sometimes" indicate economic barriers are present.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Health Canada's Household Food Security Survey Module scores
Description
Difference between intervention and comparison groups in experiences of household food insecurity. Health Canada's 18-item Household Food Security Survey Module will be used to assess experiences of marginal (1 affirmative response), moderate (2-5 affirmative responses) and severe (≥ 6 affirmative responses) household food insecurity in the past 6 months.
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Title
Diabetes Competing Demands scores
Description
Difference between intervention and comparison groups in Diabetes Competing Demands scores. The Diabetes Competing Demands 2-item scale will be used to assess the frequency of trade-offs between food, medicine, and diabetes supplies. A response of "often" or "sometimes" to either question indicates trade-offs have occurred.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Other Pre-specified Outcome Measures:
Title
MacArthur Scale of Subjective Social Status scores
Description
Difference between intervention and comparison groups in subjective social status. The MacArthur Scale of Subjective Social Status national and community ladders consist 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 nation or community. Responses can take a value from 1-10, with a higher score indicating higher subjective social status in relation to others' within ones' nation or community.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Work Productivity and Activity Impairment scores
Description
Difference between intervention and comparison groups in Work Productivity and Activity Impairment scores. The Work Productivity and Activity Impairment 6-item scale will be used to assess impairments in paid and unpaid work due to health issue(s) in the last 7 days. Four scores are calculated including absenteeism (work time missed), presenteeism (impairment at work/reduced on-the-job effectiveness), work productivity loss (overall work impairment/absenteeism + presenteeism), and activity impairment. Higher scores in each category indicate greater impairment and less productivity.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Perceived Income Adequacy
Description
Difference between intervention and comparison groups in perceived income adequacy, which is measured using a single question ("To what extent do you think your income is enough for you to live on?"). Using a 5-point response scale, scores are calculated for each participant to indicate either adequate or inadequate income.
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Title
Medication Adherence
Description
Difference between intervention and comparison groups in medication adherence. The Simple 1-item Visual Analog Scale consists of a continuum along which participants indicate how often they have taken their prescribed medication in the last 7 days. Responses range from 0% (none at all), 50% (half of prescribed doses), and 100% (all doses of prescribed medications) with higher values indicating greater medication adherence.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Physical Activity Adherence
Description
Difference between intervention and comparison groups in physical activity adherence. Patients will report on how many days during the past week they did a total of 30 minutes or more of physical activity that was enough to raise their heart rate.
Time Frame
Assessed at Baseline (0 months) and Follow-up (12 months)
Title
Subgroup analyses
Description
We will conduct subgroup analyses by gender, severity of food insecurity, rural residence, Indigenous status, baseline A1C (6.5-8.5%, 8.6-12%) and insulin use.
Time Frame
Assessed at Baseline (0 months) and Follow-up (6 months, 12 months, 18 months)
Title
Proportion of energy from ultra-processed foods
Description
Difference between intervention and comparison groups in mean proportion of energy from ultra-processed foods
Time Frame
Assessed twice at Baseline (0 months) and twice at Follow-up (6 months, 12 months, 18 months)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults (18-85 years) with type 2 diabetes (or diabetes of unknown etiology) Persistent hyperglycemia (i.e. hemoglobin A1C 6.5-12%) Are currently experiencing food insecurity and/or report that it is difficult/very difficult to make ends meet Can communicate in English or have someone to translate Exclusion Criteria: A1c <6.5% or > 12% given the recommendation for anti-hyperglycemic treatment escalation for those with A1c>12% Reside in a facility that provides meals (e.g., shelter, long-term care, prison) Exhibit signs/symptoms of metabolic decompensation (weight loss, polyuria, polydipsia) Diagnosis of eating disorder(s) (e.g., anorexia nervosa, bulimia) Have experienced diabetic ketoacidosis or a hyperglycemic hyperosmolar emergency in the past year Experienced a hypoglycemic event in the past 3 months Are trying to conceive, pregnant and/or breastfeeding Are currently participating in other clinical trials A household member is currently or has previously participated in this trial Unwilling/unable to shop in study-affiliated supermarkets for the next 12 months Plan to leave for Canada for more than 2 weeks in the next 12 months Unable to complete data collection at follow-up (e.g., due to moving)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dana Olstad, PhD, RD
Phone
403-210-8673
Email
dana.olstad@ucalgary.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Sharlette Dunn, MPH
Phone
403-210-7725
Email
sharlette.dunn2@ucalgary.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dana Olstad, PhD
Organizational Affiliation
University of Calgary
Official's Role
Principal Investigator
Facility Information:
Facility Name
Primary Care Clinics
City
Multiple Locations
State/Province
Alberta
Country
Canada
Individual Site Status
Recruiting

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35168964
Citation
Olstad DL, Beall R, Spackman E, Dunn S, Lipscombe LL, Williams K, Oster R, Scott S, Zimmermann GL, McBrien KA, Steer KJD, Chan CB, Tyminski S, Berkowitz S, Edwards AL, Saunders-Smith T, Tariq S, Popeski N, White L, Williamson T, L'Abbe M, Raine KD, Nejatinamini S, Naser A, Basualdo-Hammond C, Norris C, O'Connell P, Seidel J, Lewanczuk R, Cabaj J, Campbell DJT. Healthy food prescription incentive programme for adults with type 2 diabetes who are experiencing food insecurity: protocol for a randomised controlled trial, modelling and implementation studies. BMJ Open. 2022 Feb 15;12(2):e050006. doi: 10.1136/bmjopen-2021-050006.
Results Reference
derived

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Healthy Food Prescription Incentive Program

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