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Food Delivery, Remote Monitoring, and Coaching-Enhanced Education for Optimized Diabetes Management (FREEDOM) (FREEDOM)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Digital Health Coaching
Food Box Delivery
Remote Patient Monitoring (RPM)
Diabetes Education Class
Sponsored by
University of Alabama at Birmingham
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus, Type 2, HIV

Eligibility Criteria

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

Inclusion Criteria:

  • ≥18 years of age.
  • self-identified as the black race.
  • ICD (Implantable cardioverter-defibrillator) diagnosis of Type 2Diabetes Mellitus and either Cardiovascular disease (including coronary artery disease, stroke, or heart failure) or Chronic kidney disease referred by a primary care provider.
  • ongoing insulin treatment
  • HbA1c ≥8%
  • local area deprivation index (ADI) ≥9
  • has a PCP
  • has the ability to converse in and read English.
  • must provide written informed consent prior to enrollment.

Exclusion Criteria:

  • current enrollment in any diabetes-related interventional study.
  • cognitive impairment
  • severe untreated depression in the past 6 months
  • major cardiac events in the past 12 months
  • resting tachycardia
  • end-stage kidney disease
  • present or plans to become pregnant within 12 months
  • currently enrolled in s structured lifestyle change program or intervention.
  • All successfully screened participants must provide written informed consent prior to enrollment.

Sites / Locations

  • UAB Hospital and UMMC Cardiology ClinicsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Type

Experimental

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm 7

Arm 8

Arm Description

Digital coaching+ Food delivery+ RPM

Digital coaching

Digital coaching+ Food delivery

Digital coaching+ RPM

Food delivery+ RPM

The participant's will not receive any Intervention

Food delivery

RPM

Outcomes

Primary Outcome Measures

FREEDOM Study: Change in HbA1c level between baseline and 12 month
The primary outcome of the study is to track change in the HbA1c between baseline and 12 months (endpoint of the study). The HbA1C will be tested at baseline, 6 and 12 months.
Primary Outcome for the HIV Cohort: Change in HbA1c level between baseline and 6 months
The primary outcome of the study is to track change in the HbA1c between baseline and 6 months (endpoint of the study). The HbA1C will be tested at baseline and 6 months.

Secondary Outcome Measures

Full Information

First Posted
February 17, 2022
Last Updated
September 21, 2023
Sponsor
University of Alabama at Birmingham
Collaborators
University of Mississippi Medical Center, Cooper Green Mercy Health Systems, Pack Health
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1. Study Identification

Unique Protocol Identification Number
NCT05288452
Brief Title
Food Delivery, Remote Monitoring, and Coaching-Enhanced Education for Optimized Diabetes Management (FREEDOM)
Acronym
FREEDOM
Official Title
Food Delivery, Remote Monitoring, and Coaching-Enhanced Education for Optimized Diabetes Management (FREEDOM)
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
January 1, 2023 (Actual)
Primary Completion Date
July 1, 2026 (Anticipated)
Study Completion Date
December 1, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Alabama at Birmingham
Collaborators
University of Mississippi Medical Center, Cooper Green Mercy Health Systems, Pack Health

4. Oversight

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

5. Study Description

Brief Summary
Brief Summary: The FREEDOM study aims to develop a scalable intervention to improve type 2 diabetes mellitus control in low-income Black adults in the Deep South. The intervention targets social determinants of health (SDoH) such as reduced healthcare access, poverty, transportation barriers, and food insecurity.
Detailed Description
Detailed Description: FREEDOM Study (Type 2 Diabetes Mellitus): The FREEDOM study is a 12-month clinical trial enrolling 304 Black adults with Type 2 Diabetes Mellitus across three healthcare systems in Alabama and Mississippi. Participants are randomly assigned to one of eight combinations of three intervention components: Digital Health Coaching: Participants receive one-on-one phone-based coaching for optimized diabetes management. Food Box Delivery: Food boxes are delivered every two weeks to participants' homes, Remote Patient Monitoring (RPM): Participants receive essential supplies, including glucometers, for remote blood glucose measurement. Data is monitored remotely for timely interventions. The study involves three in-person visits at baseline, month 6, and month 12, as well as two telephone study check-ins at month 3 and 9. Survey packets are administered at each time point. FREEDOM-HIV Study (Type 2 Diabetes Mellitus and HIV Cohort): Additionally, a cohort within the study, known as the FREEDOM-HIV study, will enroll additional 80 adults who have both Type 2 Diabetes Mellitus and HIV. This cohort will be observed over a 6-month period and will also consist of the same three intervention components.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Diabetes Mellitus, Type 2, HIV

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
We used the multiphase optimization strategy (MOST) as the ideal approach for the proposed study as, with the three proposed intervention components, identifying an optimal intervention through a single randomized controlled trial (RCT) with multiple arms or through multiple RCTs would be methodologically inefficient and resource-intensive. Given this, we rely on the eloquent and rigorous MOST-based optimization design, which leverages factorial experimentation to identify an optimal set of intervention component(s). In a factorial experiment, the goal is not to compare individual experimental conditions (in this case, eight conditions), but to use combinations of conditions to estimate the main and interaction effects of the intervention components. Thus, numerous intervention components can be evaluated simultaneously while utilizing the entire randomized sample.
Masking
Investigator
Allocation
Randomized
Enrollment
304 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Digital coaching+ Food delivery+ RPM
Arm Title
Arm 2
Arm Type
Active Comparator
Arm Description
Digital coaching
Arm Title
Arm 3
Arm Type
Active Comparator
Arm Description
Digital coaching+ Food delivery
Arm Title
Arm 4
Arm Type
Active Comparator
Arm Description
Digital coaching+ RPM
Arm Title
Arm 5
Arm Type
Active Comparator
Arm Description
Food delivery+ RPM
Arm Title
Arm 6
Arm Type
Active Comparator
Arm Description
The participant's will not receive any Intervention
Arm Title
Arm 7
Arm Type
Active Comparator
Arm Description
Food delivery
Arm Title
Arm 8
Arm Type
Active Comparator
Arm Description
RPM
Intervention Type
Behavioral
Intervention Name(s)
Digital Health Coaching
Intervention Description
The digital health coaching intervention program involves an evidence-based curriculum and one-on-one support to promote positive health behaviors and patient self-management of diabetes.
Intervention Type
Dietary Supplement
Intervention Name(s)
Food Box Delivery
Intervention Description
The food box intervention component will consist of biweekly food boxes delivered directly to participants over the course of 6 months. The food boxes will contain shelf-stable groceries that adhere to ADA nutritional guidelines for individuals with T2DM.
Intervention Type
Behavioral
Intervention Name(s)
Remote Patient Monitoring (RPM)
Intervention Description
The RPM team will instruct the participants to monitor blood glucose levels 3 times daily. Glucose levels will be monitored 8 a.m. to 5 p.m.Monday to Friday. Data summaries will be reviewed bi-monthly with RNs and pharmacists. Participants will be provided with a glucometer, test strips, and mobile divide to record their blood glucose levels.
Intervention Type
Behavioral
Intervention Name(s)
Diabetes Education Class
Intervention Description
The diabetes education class will be administered by a certified diabetes educator.
Primary Outcome Measure Information:
Title
FREEDOM Study: Change in HbA1c level between baseline and 12 month
Description
The primary outcome of the study is to track change in the HbA1c between baseline and 12 months (endpoint of the study). The HbA1C will be tested at baseline, 6 and 12 months.
Time Frame
12 months
Title
Primary Outcome for the HIV Cohort: Change in HbA1c level between baseline and 6 months
Description
The primary outcome of the study is to track change in the HbA1c between baseline and 6 months (endpoint of the study). The HbA1C will be tested at baseline and 6 months.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Self-identified as Black race ICD diagnosis of T2DM ≥18 years of age Ongoing insulin treatment HbA1c ≥8% within 6 weeks of study screening SDoH local area deprivation index (ADI) ≥5 has the ability to converse in and read English must provide written informed consent prior to enrollment Exclusion criteria: Current enrollment in any diabetes-related interventional study Cognitive impairment End-stage kidney disease (CKD-5) Pregnant or plans to become pregnant within 12 months Currently enrolled in a structured lifestyle change program Enrolled in remote patient monitoring or health coaching within 60 days of the study or intervention HIV Cohort Criteria Inclusion Criteria ≥ 18 years of age ICD diagnosis of T2DM HbA1c ≥ 8% SDoH local area deprivation index (ADI) ≥ 5 Confirmed HIV+ diagnosis Prescribed HIV ART therapy as part of care Exclusion Criteria Current enrollment in any diabetes-related interventional study or structured lifestyle change program Enrolled in RPM or health coaching (except for coaching on smoking cessation) within 60 days of the intervention Cognitive impairment End-stage kidney disease (CKD-5) Pregnant or plans to become pregnant within 12 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tapan Mehta, MSEE, PhD
Phone
205-975-9171
Email
tapan@uab.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Aseel El Zein, MS, PhD, RDN
Email
aelzein@uab.edu
Facility Information:
Facility Name
UAB Hospital and UMMC Cardiology Clinics
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35205
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Destiny Taylor - for Alabama Inquiries, MPH
Phone
205-224-2567
Email
destinytaylor@uabmc.edu
First Name & Middle Initial & Last Name & Degree
Maddie Chaney - for Mississipi Inquiries, MS
Phone
601-815-8702
Email
mchaney@ummc.edu

12. IPD Sharing Statement

Plan to Share IPD
No

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Food Delivery, Remote Monitoring, and Coaching-Enhanced Education for Optimized Diabetes Management (FREEDOM)

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