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A Cognitive Behavioral Digital Therapeutic InterventiON for Glycemic Control in Type 2 Diabetes Mellitus (ACTION-DM)

Primary Purpose

Diabetes Type 2

Status
Enrolling by invitation
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
BT-001
Control Mobile Application
Sponsored by
Better Therapeutics
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Type 2

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Current (within 3 months prior to enrollment) HbA1c >=7.01%
  • Possession of and ability to use Android or iPhone mobile phone
  • Speaks and reads in English
  • Willing to measure frequent fasting finger glucose measurements as part of the App utilization

Exclusion Criteria:

  • Current use of insulin other than a long-acting insulin analogue or human NPH insulin
  • HbA1c >=11%
  • Cognitive impairment or degenerative neuropsychiatric condition (e.g. Alzheimer's, dementia, mixed dementia, other significant memory loss, schizophrenia), or any other condition that in the Investigator's opinion may prevent patient from completing study activities
  • Any terminal medical condition with life expectancy of < 1 year.

Sites / Locations

  • Mass General Brigham Hospital and Clinics

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Intervention BT-001 + Standard of Care

Standard of Care

Arm Description

Patients in this arm will receive the BT-001 treatment for up to 18 months.

Patients will have access to a control mobile application for 6 months and then will have the option to use the treatment for the remainder of the 18 month study

Outcomes

Primary Outcome Measures

Change in HbA1c
Change in HbA1c from baseline (enrollment) to 6 months after enrollment between groups.

Secondary Outcome Measures

Change in HbA1c
Change in HbA1c from baseline (enrollment) and from 6 months, to 12 months after enrollment between groups
Significant change in HbA1c
Proportion of patients with a ≥ 0.4% decrease in HbA1c at 12 months within each study group

Full Information

First Posted
March 21, 2022
Last Updated
April 7, 2022
Sponsor
Better Therapeutics
Collaborators
Mass General Brigham
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1. Study Identification

Unique Protocol Identification Number
NCT05302050
Brief Title
A Cognitive Behavioral Digital Therapeutic InterventiON for Glycemic Control in Type 2 Diabetes Mellitus
Acronym
ACTION-DM
Official Title
A Cognitive Behavioral Digital Therapeutic InterventiON for Glycemic Control in Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
March 7, 2022 (Actual)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Better Therapeutics
Collaborators
Mass General Brigham

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Randomized, controlled, pragmatic trial with open-label extension evaluating BT-001, an investigational digital therapeutic intended to help patients with type 2 diabetes improve their glycemic control.
Detailed Description
The study intervention, BT-001 (the App), will be dispensed at enrollment to the Immediate Intervention App Use arm of the trial. Patients randomized to the Delayed Intervention App Use arm will be provided a "control App" with diabetes control, and then the BT-001 App after 180 days. Each participant is assigned to one 90-day treatment cycle of BT-001. Over the 12-month intervention period, study participants will be able to opt into up to 3 additional treatment cycles of BT-001. Study schema is included at the end of this section

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study population consists of approximately 500 total participants, ages 18 - 75 years old, inclusive, who have type 2 diabetes. They will be randomized to the treatment or control group at a 3:1 ratio
Masking
None (Open Label)
Masking Description
open label
Allocation
Randomized
Enrollment
500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention BT-001 + Standard of Care
Arm Type
Active Comparator
Arm Description
Patients in this arm will receive the BT-001 treatment for up to 18 months.
Arm Title
Standard of Care
Arm Type
Other
Arm Description
Patients will have access to a control mobile application for 6 months and then will have the option to use the treatment for the remainder of the 18 month study
Intervention Type
Device
Intervention Name(s)
BT-001
Intervention Description
BT-001is a software application that delivers treatment to participants with type 2 diabetes, using behavioral therapy. BT-001 is accessed via the participants' smartphone. The behavioral intervention process involves: Identifying maladaptive thoughts based on misinformed core beliefs that lead to disease-promoting behaviors; replacing maladaptive core beliefs with adaptive ways of thinking; and providing collaborative construction of behavioral exercises to test core beliefs. Each week, BT-001 asks participants to complete a new lesson, along with one skill exercise. The lessons are expected to take between 10-20 minutes to complete. In addition to completing a lesson and skill, participants will be directed to report plant-based meals consumed and minutes of exercise completed and to measure their blood sugar daily.
Intervention Type
Device
Intervention Name(s)
Control Mobile Application
Intervention Description
The app asks patients brief questions about their health but does not include any behavioral therapy.
Primary Outcome Measure Information:
Title
Change in HbA1c
Description
Change in HbA1c from baseline (enrollment) to 6 months after enrollment between groups.
Time Frame
Baseline and Day 180
Secondary Outcome Measure Information:
Title
Change in HbA1c
Description
Change in HbA1c from baseline (enrollment) and from 6 months, to 12 months after enrollment between groups
Time Frame
Baseline and day 180, 365
Title
Significant change in HbA1c
Description
Proportion of patients with a ≥ 0.4% decrease in HbA1c at 12 months within each study group
Time Frame
Baseline and Day 365

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Current (within 3 months prior to enrollment) HbA1c >=7.01% Possession of and ability to use Android or iPhone mobile phone Speaks and reads in English Willing to measure frequent fasting finger glucose measurements as part of the App utilization Exclusion Criteria: Current use of insulin other than a long-acting insulin analogue or human NPH insulin HbA1c >=11% Cognitive impairment or degenerative neuropsychiatric condition (e.g. Alzheimer's, dementia, mixed dementia, other significant memory loss, schizophrenia), or any other condition that in the Investigator's opinion may prevent patient from completing study activities Any terminal medical condition with life expectancy of < 1 year.
Facility Information:
Facility Name
Mass General Brigham Hospital and Clinics
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02199
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
IPD will not be shared

Learn more about this trial

A Cognitive Behavioral Digital Therapeutic InterventiON for Glycemic Control in Type 2 Diabetes Mellitus

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