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Virta Intervention in CommuniTies in cOloRado (VICTOR-Pilot) (VICTOR)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Active
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Virta Health
Sponsored by
Colorado Prevention Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Community Health Workers, Nutritional Ketosis, Patient Navigator, Diabetes, Referral

Eligibility Criteria

18 Years - 79 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Able to provide electronic informed consent
  2. Age 18 - 79 years old
  3. Type 2 diabetes mellitus diagnosis by self-report and/or medical history
  4. Taking 1 or more antihyperglycemic medications
  5. Current HbA1c > 7.5%
  6. Body mass index (BMI) 25 kg/m2 or greater
  7. Capable of engaging in virtual care

Exclusion Criteria:

  1. Type 1 diabetes
  2. Pregnant or planning pregnancy within the next 9 months
  3. Lactating
  4. Admission for diabetic ketoacidosis (DKA) or hyperglycemic hyperosmolar syndrome (HHS) within the last 12 months
  5. Life expectancy <1 year
  6. Postural orthostatic tachycardia syndrome (POTS) and/or recurrent syncope
  7. Active severe psychiatric or medical condition(s) such as advanced renal (end-stage renal disease or CKD stage 4 or 5; eGFR <30 mL/min), cardiac (NYHA Class 4 heart failure), or hepatic dysfunction (Child-Pugh Class C)
  8. Any condition which in the opinion of the investigator would make the study unsuitable for the subject including investigator opinion regarding inability to comply with Virta instructions

Sites / Locations

  • Northwest Colorado Health - Community Health Center & Prevention Services Craig
  • High Plains Community Health Center
  • Chaffee County Public and Environmental Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Nutritional Ketosis Intervention Referral

CHHS Standard Care - Delayed Referral to Nutritional Ketosis Intervention

Arm Description

The comprehensive remotely-delivered continuous remote care to induce nutritional ketosis combined with remote medication management is the Virta treatment, and while on this treatment, subjects will have access to Virta health coaches and licensed medical providers who will perform medical therapy management, health coaching, nutrition and behavior change education, biometric feedback, and the option to participate in a community for peer support.

All subjects will be enrolled in Colorado Heart Healthy Solutions (CHHS), which consists of community health worker (CHW) contact and sessions on: 1) cardiovascular disease knowledge; 2) Health behavior change through skill building to improve diet (e.g., portion sizes, increasing fruit/vegetable intake, reducing intake of sugar sweetened beverages, decreasing fast food meals, etc.), increase physical activity, and improve well-being, tailored to individual subjects' risk profile and self-identified goals; and 3) Connection to services including primary care, mental health services if needed, and relevant community programs to address barriers (e.g. food insecurity, need for legal help) or to promote behavior change (e.g. free/low cost exercise programs).

Outcomes

Primary Outcome Measures

Change in hemoglobin A1c (Percent)
Change from baseline hemoglobin A1c (Percent) among patients referred to continuous remote care (Group 1) versus standard care (Group 2)

Secondary Outcome Measures

Change in BMI
Among Group 1 versus Group 2 subjects, change in body mass index (kg/m2)
Change in hemoglobin A1c
Among Group 1 versus Group 2 subjects, difference in hemoglobin A1c
Change in number and/or doses of anti-hyperglycemic medications • doses of anti-hyperglycemic medications
Among Group 1 versus Group 2 subjects, difference in: number of anti-hyperglycemic medications doses of anti-hyperglycemic medications

Full Information

First Posted
March 16, 2021
Last Updated
September 6, 2023
Sponsor
Colorado Prevention Center
Collaborators
Virta Health
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1. Study Identification

Unique Protocol Identification Number
NCT04807218
Brief Title
Virta Intervention in CommuniTies in cOloRado (VICTOR-Pilot)
Acronym
VICTOR
Official Title
Virta Intervention in CommuniTies in cOloRado (VICTOR-Pilot) Pilot Study to Improve Diabetes and Cardiovascular Risk in Rural Communities
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
March 2, 2021 (Actual)
Primary Completion Date
December 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Colorado Prevention Center
Collaborators
Virta 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
The VICTOR study plans to include rural communities served by Colorado Heart Healthy Solutions (CHHS) program and find out whether participants will accept a referral to a comprehensive virtual lifestyle intervention, Virta Health. The Virta Health program induces nutritional ketosis to improve glucose control in individuals with type 2 diabetes. The study will inform the acceptability of the referral, the retention of participants in lifestyle intervention, and the durability of effects on glucose control after the lifestyle intervention has ended.
Detailed Description
In rural communities served by Colorado Heart Healthy Solutions (CHHS), referral to a comprehensive remotely-delivered (virtual) continuous remote care to induce nutritional ketosis combined with remote medication management will improve glycemic control in patients with type 2 diabetes as compared with standard care. The study intervention is the referral. Subjects are not mandated to receive Virta treatment and are welcome to continue in the study whether or not the referral is accepted. 2 rural communities served by CHHS have been chosen as recruitment sites. Study patients will be randomized at the site level. Objectives Primary: To assess glycemic control in patients with type 2 diabetes living in a rural community referred to a comprehensive remotely-delivered continuous remote care to induce nutritional ketosis combined with remote medication management (termed "continuous remote care") as compared with those living in a rural community offered standard care. Secondary: To assess the effects of referral to continuous remote care as compared with standard care on body weight and on body mass index To assess the effects of referral to continuous remote care as compared with standard care on number and doses of anti-hyperglycemic medications To determine the durability of a continuous remote care intervention when paired with ongoing community health worker support Exploratory: To assess the effects of referral to continuous remote care as compared with standard care on LDL-cholesterol, fasting glucose, and fasting triglyceride/HDL-cholesterol ratio To assess patient-reported outcomes of continuous remote care as compared with standard care To determine enrollment rate (offered vs accepted) in patients with type 2 diabetes living in rural communities referred to continuous remote care. To determine active engagement (number, timing, and types of 2-way contacts) and retention in patients with type 2 diabetes living in rural communities referred to continuous remote care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Community Health Workers, Nutritional Ketosis, Patient Navigator, Diabetes, Referral

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nutritional Ketosis Intervention Referral
Arm Type
Active Comparator
Arm Description
The comprehensive remotely-delivered continuous remote care to induce nutritional ketosis combined with remote medication management is the Virta treatment, and while on this treatment, subjects will have access to Virta health coaches and licensed medical providers who will perform medical therapy management, health coaching, nutrition and behavior change education, biometric feedback, and the option to participate in a community for peer support.
Arm Title
CHHS Standard Care - Delayed Referral to Nutritional Ketosis Intervention
Arm Type
Active Comparator
Arm Description
All subjects will be enrolled in Colorado Heart Healthy Solutions (CHHS), which consists of community health worker (CHW) contact and sessions on: 1) cardiovascular disease knowledge; 2) Health behavior change through skill building to improve diet (e.g., portion sizes, increasing fruit/vegetable intake, reducing intake of sugar sweetened beverages, decreasing fast food meals, etc.), increase physical activity, and improve well-being, tailored to individual subjects' risk profile and self-identified goals; and 3) Connection to services including primary care, mental health services if needed, and relevant community programs to address barriers (e.g. food insecurity, need for legal help) or to promote behavior change (e.g. free/low cost exercise programs).
Intervention Type
Behavioral
Intervention Name(s)
Virta Health
Intervention Description
The comprehensive remotely-delivered continuous remote care to induce nutritional ketosis combined with remote medication management is the Virta treatment, and while on this treatment, subjects will have access to Virta health coaches and licensed medical providers who will perform medical therapy management, health coaching, nutrition and behavior change education, biometric feedback, and the option to participate in a community for peer support.
Primary Outcome Measure Information:
Title
Change in hemoglobin A1c (Percent)
Description
Change from baseline hemoglobin A1c (Percent) among patients referred to continuous remote care (Group 1) versus standard care (Group 2)
Time Frame
3.5 months
Secondary Outcome Measure Information:
Title
Change in BMI
Description
Among Group 1 versus Group 2 subjects, change in body mass index (kg/m2)
Time Frame
Baseline versus 3.5 months, 3.5 months versus 7 months, baseline versus10 months
Title
Change in hemoglobin A1c
Description
Among Group 1 versus Group 2 subjects, difference in hemoglobin A1c
Time Frame
3.5 months versus 7 months, baseline versus 10 months
Title
Change in number and/or doses of anti-hyperglycemic medications • doses of anti-hyperglycemic medications
Description
Among Group 1 versus Group 2 subjects, difference in: number of anti-hyperglycemic medications doses of anti-hyperglycemic medications
Time Frame
Baseline versus 3.5 months, 3.5 months versus 7 months, baseline versus 10 months
Other Pre-specified Outcome Measures:
Title
Acceptance of referral to continuous remote care
Description
Proportion agreeing to participate in continuous remote care in Group 1 at baseline versus at 3.5 months in Group 2
Time Frame
Baseline in Group 1 versus 3.5 months in Group 2
Title
Change in fasting triglyceride/HDL ratio
Description
Among Group 1 versus Group 2 subjects, change from in fasting triglyceride/HDL ratio
Time Frame
Baseline versus 3.5 months, 3.5 months versus 7 months, baseline versus 10 months
Title
Change in LDL-cholesterol
Description
Among Group 1 versus Group 2 subjects, change from in LDL-cholesterol
Time Frame
Baseline versus 3.5 months, 3.5 months versus 7 months, baseline versus 10 months
Title
Change in fasting glucose
Description
Among Group 1 versus Group 2 subjects, change from in fasting glucose
Time Frame
Baseline versus 3.5 months, 3.5 months versus 7 months, baseline versus 10 months
Title
Acceptance/continuation of referral to continuous remote care
Description
Among Group 1 subjects, proportion agreeing to participate in continuous remote care
Time Frame
Baseline and 3.5 months
Title
Continuation of referral in Group 1 versus acceptance of referral in Group 2
Description
Among Group 1 versus Group 2 subjects, proportion agreeing to participate/continue in continuous remote care
Time Frame
3.5 months
Title
Change in perceived health status
Description
Among Group 1 and Group 2 subjects, evaluation over time (i.e. 3 months post-intervention) in perceived health status as assessed by question 1 of the Short Form Health Survey (SF-1).
Time Frame
Baseline, 3.5 months, 7 months and 10 months
Title
Change in diabetes treatment satisfaction
Description
Among Group 1 and Group 2 subjects, evaluation over time at baseline, in diabetes treatment satisfaction as assessed by the Diabetes Treatment Satisfaction Questionnaire. The scale for the survey questions is 0-6. In general, a higher score indicates a higher level of satisfaction with diabetic treatment.
Time Frame
Baseline, 3.5 months, 7 months and 10 months
Title
Count of 2-way contacts among subjects
Description
Among Group 1 and Group 2 subjects, evaluation in active engagement as assessed by number of 2-way contacts.
Time Frame
3.5 months and 7 months
Title
Acceptability of referral
Description
Among Group 1 subjects at baseline 3.5 and 7 months, and Group 2 subjects at 3.5 and 7 months. Participants will be asked 'Did you complete the referral to Virta Health?' Yes/No
Time Frame
Group 1: baseline, 3.5 months and 7 months / Group 2: 3.5 months and 7 months
Title
Acceptability of referral over time
Description
Among Group 1 subjects at baseline 3.5 and 7 months, and Group 2 subjects at 3.5 and 7 months. Participants will be asked if they are still continuing their treatment with Virta Health.
Time Frame
Group 1: baseline, 3.5 months and 7 months / Group 2: 3.5 months and 7 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Able to provide electronic informed consent Age 18 - 79 years old Type 2 diabetes mellitus diagnosis by self-report and/or medical history Taking 1 or more antihyperglycemic medications Current HbA1c > 7.5% Body mass index (BMI) 25 kg/m2 or greater Capable of engaging in virtual care Exclusion Criteria: Type 1 diabetes Pregnant or planning pregnancy within the next 9 months Lactating Admission for diabetic ketoacidosis (DKA) or hyperglycemic hyperosmolar syndrome (HHS) within the last 12 months Life expectancy <1 year Postural orthostatic tachycardia syndrome (POTS) and/or recurrent syncope Active severe psychiatric or medical condition(s) such as advanced renal (end-stage renal disease or CKD stage 4 or 5; eGFR <30 mL/min), cardiac (NYHA Class 4 heart failure), or hepatic dysfunction (Child-Pugh Class C) Any condition which in the opinion of the investigator would make the study unsuitable for the subject including investigator opinion regarding inability to comply with Virta instructions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Cecilia Low Wang, MD
Organizational Affiliation
CPC Clinical Research
Official's Role
Principal Investigator
Facility Information:
Facility Name
Northwest Colorado Health - Community Health Center & Prevention Services Craig
City
Craig
State/Province
Colorado
ZIP/Postal Code
81625
Country
United States
Facility Name
High Plains Community Health Center
City
Lamar
State/Province
Colorado
ZIP/Postal Code
81052
Country
United States
Facility Name
Chaffee County Public and Environmental Health
City
Salida
State/Province
Colorado
ZIP/Postal Code
81201
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
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Virta Intervention in CommuniTies in cOloRado (VICTOR-Pilot)

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