- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05228860
Addressing Diabetes by Elevating Access to Nutrition (ADELANTE)
Addressing Diabetes by Elevating Access to Nutrition: the ADELANTE Study
The goal of ADELANTE is to determine whether a multi-level intervention to improve household food insecurity and glycemic control is effective for Latino patients with diabetes.
Specifically, ADELANTE aims to
- determine whether weekly household food delivery plus an intensive lifestyle intervention is more effective than usual care for improving glycemic control (HbA1c) at 6 months,
- examine the effects of the multi-level intervention on = household food insecurity, dietary behaviors, and psychosocial outcomes, and
- assess the future potential for implementation and dissemination of this multi-level intervention in primary care settings.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Participants and up to two of their household members will be randomized to one of two groups:
- healthy food box home delivery for 12 weeks plus a 12-month remotely delivered lifestyle behavioral intervention, Vida Sana, which incorporates family members and is aligned with Latino cultural values, or
- a wait list control group who will receive the food box deliveries 6 months later (but not the Vida Sana intervention).
The first 6 months will evaluate the effects of receiving Vida Sana plus food delivery versus being randomized to control (no intervention); the final 6 months will evaluate receiving food delivery with versus without Vida Sana.
VIDA SANA (intervention arm):
The Vida Sana intervention is a cultural adaptation of Group Lifestyle Balance, a 12-month group program in turn adapted from the NIH/NIDDK-supported Diabetes Prevention Program (DPP). It has been shown to be effective in promoting clinically significant, modest weight loss and significant improvements in moderate-intensity physical activity. Participants receive a total of 23 group sessions over 12 months with a trained health coach who provides personalized feedback based on self-tracking.
The program emphasizes a) moderate caloric reduction by 500-1,000 calories per day through healthy substitutions, b) incremental increases in moderate physical activity such as brisk walking, and c) behavioral strategies to support successful adoption and maintenance of healthy behaviors. These behavioral strategies include realistic goal setting, fostering social support, and stress management. Study health coaches will also add COVID-specific topics to ensure that participants are equipped to change behavior and manage stress during the pandemic.
FOOD BOXES (intervention arm (immediately) and control arm (6 months later)):
Each healthy food box delivery will include a variety of seasonal produce and a rotation of different whole grain foods (3+ grams of fiber/serving) such as cereal, pasta, tortillas, bread, and crackers. Participants will receive familiar foods as well as (intentionally) unfamiliar items to encourage them to try new foods. All items are also available at low-cost grocery stores so participants can continue to purchase them after the end of the study if they wish. The quantity is scaled to three household sizes. It is intended to supplement a family's food supply and provide opportunities for trying new fiber-rich foods recommended by the Vida Sana intervention.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Study Coordinator
- Phone Number: 650-725-5180
- Email: morizaga@stanford.edu
Study Locations
-
-
California
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Concord, California, United States, 94518
- Recruiting
- La Clínica Monument
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
For main study (index/intervention) participants:
- Age at enrollment: 18+ years
- Self-identified ethnicity: Hispanic, Latino, Chicano, or Spanish
- Type 2 diabetes indicated in the electronic health record, e.g. as ICD-10 (International Classification of Diseases) diagnosis code or HbA1c value
- Have indicated food insecurity according to the screening 2-item Hunger Vital Sign questionnaire
- Have a Body Mass Index (BMI) => 25
- Receiving care at our partnering community health centers (e.g., Clinica de la Raza)
- Currently residing in Alameda or Contra Costa County and not expecting to relocate in the next 6-12 months
- Have access to phone or computer, email, and some internet for access to remote intervention and completion of follow-up measures
For household members:
- Age at enrollment: 12+ years
- Significantly involved in supporting nutrition in the home including food shopping, preparation, social support for healthy nutrition
- Willing to complete some questionnaires and attend a single group session.
For all participants:
- Able and willing to provide informed consent
Exclusion Criteria:
- Unable to provide informed consent
- Unable to speak, read, or understand English and/or Spanish
- Active substance use or psychotic disorders that would impair participation in a group lifestyle intervention or interfere with follow-up assessments
- Lacking mailing address for delivery of food box
- Planning to relocate out of area within the next 12 months
- Index participant only: Pregnant or planning to become pregnant within the next 12 months
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Food and Lifestyle Intervention Group
The Food and Lifestyle Intervention Group will receive weekly household deliveries of healthy food as well as a lifestyle intervention (called Vida Sana) that will be delivered via Zoom and facilitated by a trained bilingual/bicultural health coach.
|
Vida Sana is a Group Lifestyle intervention that has been shown to be effective among patients with type 2 diabetes (T2DM). Vida Sana includes 23 group sessions with a trained health coach:
All regular primary care and diabetes care will remain as usual. Participants will receive 12 weeks of weekly food deliveries from Dig Deep Farms. Each delivery will include a selection of seasonal fresh vegetables and a rotation of either a whole grain or a whole-grain food (3+ grams of fiber/serving). Whole grains will include brown rice, oatmeal, barley, quinoa; whole grain foods will include cereal, pasta, tortillas, bread, crackers. Delivery sizes will be scaled to the three corresponding household sizes: 2-3 people; 4-5 people; or 6 or more people. Food will be delivered by Dig Deep Farms, which already has an established food subscription delivery system. (Control group participants will receive the same delivery schedule, but delayed to begin 6 months after their study enrollment.) |
|
Experimental: Waitlist Control Group
The waitlist control will continue usual care with no intervention for 6 months.
To balance rigor with ethical considerations, they will receive the healthy food box deliveries after a 6 month waiting period.
|
Participants will receive 12 weeks of weekly food deliveries from Dig Deep Farms. Each delivery will include a selection of seasonal fresh vegetables and a rotation of either a whole grain or a whole-grain food (3+ grams of fiber/serving). Whole grains will include brown rice, oatmeal, barley, quinoa; whole grain foods will include cereal, pasta, tortillas, bread, crackers. Delivery sizes will be scaled to the three corresponding household sizes: 2-3 people; 4-5 people; or 6 or more people. Food will be delivered by Dig Deep Farms, which already has an established food subscription delivery system. (Control group participants will receive the same delivery schedule, but delayed to begin 6 months after their study enrollment.) |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
HgbA1c
Time Frame: Baseline through 12 months post-enrollment
|
Study staff will gather fingerstick blood samples for HgbA1c.
|
Baseline through 12 months post-enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
nonHDL Cholesterol
Time Frame: Baseline through 12 months post-enrollment
|
Study staff will gather fingerstick blood samples for lipid measurements, focusing on non- HDL cholesterol (total minus HDL cholesterol) which is a valuable marker of atherogenic dyslipidemia in diabetic individuals that does not require a fasting state.
|
Baseline through 12 months post-enrollment
|
|
Blood Pressure
Time Frame: Baseline through 12 months post-enrollment
|
Blood pressure will be measured with an automated cuff with digital readout, or using a traditional sphygmomanometer.
A study staff member will conduct the reading.
Both systolic and diastolic pressure will be measured.
|
Baseline through 12 months post-enrollment
|
|
Change in Body Mass Index (BMI)
Time Frame: Baseline through 12 months post-enrollment
|
Weight (kg) and height (cm) will be measured and Body Mass Index (BMI) will be calculated in kg/m^2.
Height and weight will be gathered using standardized protocols with a portable scale and stadiometer.
At baseline, these will be measured in triplicate for accuracy.
|
Baseline through 12 months post-enrollment
|
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Change in waist-height ratio
Time Frame: Baseline through 12 months post-enrollment
|
Waist-height ratio (cm) will be calculated and compared over time.
Waist circumference (cm) will be measured at iliac crest.
Height (cm) will be measured using standardized protocols.
|
Baseline through 12 months post-enrollment
|
|
Pandemic-Related Perceived Stress Scale of COVID-19 (PSS-10-C)
Time Frame: Baseline through 12 months post-enrollment
|
Participants will answer 10 questions about their stress related to the pandemic. Scale is made up of 10 items, each of which offers five response options: never, almost never, occasionally, almost always and always. Items 1, 2, 3, 6, 9 and 10 are scored directly from 0 to 4 and items 4, 5, 7 and 8, conversely, from 4 to 0. Scores range from 0 to 40, higher scores indicating greater stress. The PSS-10-C was adapted from the Scale of Perceived Stress (PSS-10) and independently validated during March 2020 in response to government-mandated COVID-19 quarantines in Columbia (see Campo-Arias et al 2020 in the references section) |
Baseline through 12 months post-enrollment
|
|
Type 2 Diabetes Mellitus Related Stress
Time Frame: Baseline through 12 months post-enrollment
|
Diabetes-related stress will be measured using the validated 20-item Problem Areas in Diabetes Survey (PAID) questionnaire. Each item is scored from 0 (not a problem) to 4 (serious problem). The sum of all item scores multiplied by 1.25 gives the total PAID score. Scores range from 0 to 100, higher scores reflecting greater emotional distress. |
Baseline through 12 months post-enrollment
|
|
Health-related quality of life (adult participants only)
Time Frame: Baseline through 12 months post-enrollment
|
Index participants and adult household members will receive the Short Form-8 (SF-8) questionnaire. SF-8 is an 8-item instrument that measures general aspects of health-related quality of life. Each item covers a different domain: overall health, physical functioning, role physical (difficulties with daily work because of physical pain), bodily pain, vitality, social functioning, mental health, and role emotional (absence from daily activities because of emotional problems). Items are assessed individual 5- or 6-point Likert scales, a higher score on each question indicates poorer quality of life in that domain. |
Baseline through 12 months post-enrollment
|
|
Health-related quality of life (adolescent household members only)
Time Frame: Baseline through 12 months post-enrollment
|
Instead of the SF-8 (see previous outcome), adolescent household members will receive the Kid-Screen-10, a questionnaire is designed for children ages 8-18 to assess subjective health and psychological, mental, and social well-being. Scores range from 10 to 50, with higher scores indicating higher health-related quality of life. |
Baseline through 12 months post-enrollment
|
|
Depression
Time Frame: Baseline through 12 months post-enrollment
|
Possible depression will be measured using the Patient Health Questionnaire (PHQ-8), which measures 8 criteria from the DSM-IV (Diagnostic and Statistical Manual of Mental Disorders).
Each criteria is scored from "0" (not at all) to "3" (nearly every day).
Range is 0-24, higher total score indicates more severe depression.
|
Baseline through 12 months post-enrollment
|
|
Depression (index participant only)
Time Frame: Baseline through 12 months post-enrollment
|
For index participants, depression will be measured using the Patient Health Questionnaire (PHQ-9), which measures 8 criteria from the DSM-IV (Diagnostic and Statistical Manual of Mental Disorders) and a ninth question on suicidal thoughts.
Each criteria is scored from "0" (not at all) to "3" (nearly every day).
Range is 0-27, higher total score indicates more severe depression.
|
Baseline through 12 months post-enrollment
|
|
Anxiety
Time Frame: Baseline through 12 months post-enrollment
|
Level of anxiety will be measured using the General Anxiety Disorder-7 (GAD-7).
This is a 7 item instrument that uses some of the DSM-V (Diagnostic and Statistical Manual of Mental Disorders) criteria for General Anxiety Disorder along with measuring anxiety symptom severity.
Scores range from 0 to 21, higher scores indicate more severe anxiety.
|
Baseline through 12 months post-enrollment
|
|
Dietary Intake Over 24 Hour Period (index participants only)
Time Frame: Baseline through 12 months post-enrollment
|
Index participants will complete three 24-hour diet recalls using the Automated Self-Administered 24-hour (ASA24®) Dietary Assessment Tool. The module includes multiple-pass methodology to capture all foods eaten in the previous 24 hours. A researcher will administer the tool to reduce respondent burden. Output for 24-hour diet recall is extensive, but will include our key dietary outcomes for daily (averaged) intakes of: total vegetables, dark green vegetables, beans/legumes, and whole grains. Scores: Healthy Eating Index (HEI): 0 to 100, higher indicates greater alignment with healthy dietary guidelines Fruit & vegetable: 0-20 servings/day, higher scores preferred Total calorie intake: 1000-6000 kcal/day Total fat: 0-400 g/day Interview method adapted from Conway et al 2004 (see references section). |
Baseline through 12 months post-enrollment
|
|
Dietary Intake (household members only)
Time Frame: Baseline through 12 months post-enrollment
|
Household members will be given the 10-item Dietary Screener Questionnaire (DSQ-10). The questionnaire will capture consumption of fruit/vegetables, fiber, whole grains, and added sugars. Scores range from 0 to 100, higher scores indicate more frequent consumption of healthy foods. They will also be asked additional questions about whole grain foods, which will be scored the same way. These will be based on the dietary screener developed by Thompson and colleagues (see Thompson et al 2017 in references section). |
Baseline through 12 months post-enrollment
|
|
Diet-Related Behaviors: Food Preferences & Consumption
Time Frame: Baseline through 12 months post-enrollment
|
We will create a multi-part questionnaire to assess diet-related behaviors:
|
Baseline through 12 months post-enrollment
|
|
Changes in Diet-Related Behaviors
Time Frame: 6 months through 12 months post-enrollment
|
Participants will be asked a series of questions designed by the research team to examine changes in their whole grain and vegetable consumption over the past 6 months.
Higher score is generally a better outcome as it indicates increase in consumption of these healthy foods.
|
6 months through 12 months post-enrollment
|
|
Change in physical activity
Time Frame: Baseline through 12 months post-enrollment
|
Using the 7-day Physical Activity Recall, each participant will complete a semi-structured interview that estimates their time spent doing physical and sleep activities in the past 7 days. Scores are:
|
Baseline through 12 months post-enrollment
|
|
Food Neophobia Scale (FNS)
Time Frame: Baseline through 12 months post-enrollment
|
Comprises 10 items to which responses are given on a seven-point Likert scale ranging from "strongly disagree" to "strongly agree." Score ranges from 10 to 70, a higher total score indicates greater food neophobia level and lower tendency to try unfamiliar foods. |
Baseline through 12 months post-enrollment
|
|
Control Over Food Choices
Time Frame: Baseline through 12 months post-enrollment
|
Participants will be asked a three part-questionnaire about control and food choices in the past 6 months:
|
Baseline through 12 months post-enrollment
|
|
Nutrition Security Screener
Time Frame: Baseline through 12 months post-enrollment
|
The Nutrition Security Screener (NSS) was developed by Tufts University, Kaiser Permanente, and Los Angeles Department of Public Health. The questionnaire contains 14 questions, divided into two sections:
Question 1 will be scored on a scale of 1-4 to indicate if food security is very low, low, marginal, or secure. Measure designers have not validated a scale for question 2, so it will be analyzed descriptively. |
Baseline through 12 months post-enrollment
|
|
Interest in Community Supported Agriculture (CSA) Programs
Time Frame: Baseline through 12 months post-enrollment
|
Community Supported Agriculture (CSA) is a local farm-to-table model where customers can sign up for a subscription with a local farm and receive a weekly box of seasonal fruits and vegetables. Participants will be asked a 4 item questionnaire to gauge their experiences with, and interest in, such food boxes, including how much they would be willing to spend for one (e.g. $10-20 per bag). There is no scoring rubric, results are descriptive. |
Baseline through 12 months post-enrollment
|
|
Household Food Insecurity
Time Frame: Baseline through 12 months post-enrollment
|
Each participant will complete the USDA's U.S. Household Food Security Survey Module: Six-Item Short Form to measure household food security. Raw scores are converted into food security status as follows: 0-1 indicates high or marginal food security, 2-4 indicates low food security, and 5-6 indicates very low food security. |
Baseline through 12 months post-enrollment
|
|
Food Assistance Programs
Time Frame: Baseline through 12 months post-enrollment
|
Participants are asked whether their household currently receives (or has received in the past 6 months) various sorts of food assistance, such as:
There is no scoring rubric, results are descriptive. |
Baseline through 12 months post-enrollment
|
|
Self-reported Loneliness
Time Frame: Baseline through 12 months post-enrollment
|
The validated UCLA 3 item Loneliness Scale will be used. The scale is designed to measure one's subjective feelings of loneliness as well as feelings of social isolation. Participants rate each item as "hardly ever" (1), "some of the time" (2), or "often" (3). Scores range from 3 to 9, higher scores indicate greater levels of loneliness. |
Baseline through 12 months post-enrollment
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lisa Goldman Rosas, PhD, MPH, Stanford University
Publications and helpful links
General Publications
- Russell DW. UCLA Loneliness Scale (Version 3): reliability, validity, and factor structure. J Pers Assess. 1996 Feb;66(1):20-40. doi: 10.1207/s15327752jpa6601_2.
- Polonsky WH, Anderson BJ, Lohrer PA, Welch G, Jacobson AM, Aponte JE, Schwartz CE. Assessment of diabetes-related distress. Diabetes Care. 1995 Jun;18(6):754-60. doi: 10.2337/diacare.18.6.754.
- Sallis JF, Grossman RM, Pinski RB, Patterson TL, Nader PR. The development of scales to measure social support for diet and exercise behaviors. Prev Med. 1987 Nov;16(6):825-36. doi: 10.1016/0091-7435(87)90022-3.
- Zuazagoitia A, Montoya I, Grandes G, Arietaleanizbeascoa MS, Arce V, Martinez V, Sanchez M, Sanchez A. Reliability and validity of the 7-day Physical Activity Recall interview in a Spanish population. Eur J Sport Sci. 2014;14 Suppl 1:S361-8. doi: 10.1080/17461391.2012.705332. Epub 2012 Jul 25.
- Conway JM, Ingwersen LA, Moshfegh AJ. Accuracy of dietary recall using the USDA five-step multiple-pass method in men: an observational validation study. J Am Diet Assoc. 2004 Apr;104(4):595-603. doi: 10.1016/j.jada.2004.01.007.
- Blair SN, Haskell WL, Ho P, Paffenbarger RS Jr, Vranizan KM, Farquhar JW, Wood PD. Assessment of habitual physical activity by a seven-day recall in a community survey and controlled experiments. Am J Epidemiol. 1985 Nov;122(5):794-804. doi: 10.1093/oxfordjournals.aje.a114163.
- Sarkar U, Schillinger D, Lopez A, Sudore R. Validation of self-reported health literacy questions among diverse English and Spanish-speaking populations. J Gen Intern Med. 2011 Mar;26(3):265-71. doi: 10.1007/s11606-010-1552-1. Epub 2010 Nov 6.
- Domel SB, Baranowski T, Davis H, Leonard SB, Riley P, Baranowski J. Measuring fruit and vegetable preferences among 4th- and 5th-grade students. Prev Med. 1993 Nov;22(6):866-79. doi: 10.1006/pmed.1993.1078.
- Ellison B, McFadden B, Rickard BJ, Wilson N. Examining food purchase behavior and food values during the COVID-19 pandemic. Applied Economic Perspectives and Policy. 2021;43(1):58-72. http://dx.doi.org/10.1002/aepp.13118
- Marin G, Gamba RJ. A new measurement of acculturation for Hispanics: The Bidimensional Acculturation Scale for Hispanics (BAS). Hispanic Journal of Behavioral Sciences. 1996;18(3):297-316. http://dx.doi.org/10.1177/07399863960183002
- Thompson FE, Midthune D, Kahle L, Dodd KW. Development and Evaluation of the National Cancer Institute's Dietary Screener Questionnaire Scoring Algorithms. J Nutr. 2017 Jun;147(6):1226-1233. doi: 10.3945/jn.116.246058. Epub 2017 May 10.
- Calloway EE, Carpenter LR, Gargano T, Sharp JL, Yaroch AL. Development of new measures to assess household nutrition security, and choice in dietary characteristics. Appetite. 2022 Dec 1;179:106288. doi: 10.1016/j.appet.2022.106288. Epub 2022 Aug 29.
- Campo-Arias A, Pedrozo-Cortes MJ, Pedrozo-Pupo JC. Pandemic-Related Perceived Stress Scale of COVID-19: An exploration of online psychometric performance. Rev Colomb Psiquiatr (Engl Ed). 2020 Oct-Dec;49(4):229-230. doi: 10.1016/j.rcp.2020.05.005. Epub 2020 Jul 17. No abstract available. English, Spanish.
Helpful Links
- Environmental Influences on Child-wide Health Outcomes (ECHO). COVID-19 Questionnaire - Adult Primary Version. ECHO-wide Cohort Version 01.30. April 9, 2020. Published 2020.
- Tuft University Friedman School of Nutrition Science & Policy. Public Impact Initiative: Food is Medicine. Resources Page. Accessed April 20, 2023.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 62283
- 1R01MD016738-01 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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