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RAE (Realize, Analyze, Engage)

Primary Purpose

Substance Use Disorders, Treatment Adherence and Compliance

Status
Recruiting
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
RAE
Sponsored by
ContinueYou, LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Substance Use Disorders focused on measuring mhealth, stress, craving, wearables, technology, digital diagnostics, digital health

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years or older
  • Enrolled in an outpatient SUD treatment program
  • Enrolled in treatment for < 90 days
  • Fluent in English
  • Have access to a smartphone with iOS or Android Capabilities
  • Capable of providing informed consent

Exclusion Criteria:

  • Pregnancy
  • Prisoner Status
  • Significant limitation of range of motion of non-dominant arm (amputation or fracture)

Sites / Locations

  • University of Massachusetts Chan Medical SchoolRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Interventional (RAE + Usual Care)

Control (Usual care)

Arm Description

Subjects will receive usual care through an outpatient substance use disorder treatment facility, will be provided with a wearable sensor and the RAE mobile application. Participants will be instructed to use the RAE app for a minimum of 30 days.

Subjects will receive usual care through an outpatient substance use disorder treatment facility and will be provided with a wearable sensor (fitness tracker). They will not be given access to the RAE mobile app.

Outcomes

Primary Outcome Measures

Number of participants with return to drug use
Relapse to use of substance use defined as 1) self-reported use, 2) positive urine drug screen (from treatment program) or 3) provider report of confirmed relapse (Only applies to substances for which subject is receiving treatment)

Secondary Outcome Measures

Number of participants retained in treatment
Participants status as engaged in recovery treatment (index treatment program or other)
Number of hospitalizations and emergency department visits per participant
Includes absolute number of Emergency Department visits (SUD and non-SUD related), number of unplanned hospital admissions (SUD and non-SUD related), number of days hospitalized (SUD and non-SUD related admissions) and overdose related visits

Full Information

First Posted
January 25, 2022
Last Updated
April 5, 2023
Sponsor
ContinueYou, LLC
Collaborators
University of Massachusetts, Worcester, University of Texas at Tyler
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1. Study Identification

Unique Protocol Identification Number
NCT05227339
Brief Title
RAE (Realize, Analyze, Engage)
Official Title
RAE (Realize, Analyze, Engage)- A Digital Biomarker Based Detection and Intervention System for Stress and Craving During Recovery From Substance Use Disorder: Phase II
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 22, 2023 (Actual)
Primary Completion Date
April 1, 2024 (Anticipated)
Study Completion Date
April 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
ContinueYou, LLC
Collaborators
University of Massachusetts, Worcester, University of Texas at Tyler

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The proposed study will evaluate the detection of digital biomarkers of stress, and drug craving in a population of individuals undergoing treatment for substance use disorder
Detailed Description
RAE integrates digital detection of high-risk stress and craving periods by utilizing a mobile phone application and integrated wearable sensor. These detections are paired with interventions (mindfulness based de-escalation tools), support, and monitoring (to identify trends and plan for future). The present study will deploy the technology in a multi-site randomized controlled trial to test the efficacy of the RAE system in on clinical and psychosocial outcomes. Subjects will be randomized to use the RAE system (mobile app and wearable sensor) plus usual care vs usual care plus a fitness tracker only to measure differences retention in treatment, return to substance use, and overall psychosocial functioning. The ultimate goal is to develop a cost-effective, paradigm changing recovery tool that will improve substance use disorder treatment, and prevent related complications and deaths.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance Use Disorders, Treatment Adherence and Compliance
Keywords
mhealth, stress, craving, wearables, technology, digital diagnostics, digital health

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Interventional (RAE + Usual Care)
Arm Type
Experimental
Arm Description
Subjects will receive usual care through an outpatient substance use disorder treatment facility, will be provided with a wearable sensor and the RAE mobile application. Participants will be instructed to use the RAE app for a minimum of 30 days.
Arm Title
Control (Usual care)
Arm Type
No Intervention
Arm Description
Subjects will receive usual care through an outpatient substance use disorder treatment facility and will be provided with a wearable sensor (fitness tracker). They will not be given access to the RAE mobile app.
Intervention Type
Device
Intervention Name(s)
RAE
Other Intervention Name(s)
RAE Mobile App
Intervention Description
Subjects in the interventional group will have access to the RAE Health mobile app which receives continuous physiologic data from a wearable device. Algorithms embedded in the RAE app detect stress and craving events, and trigger mobile phone notifications when detected. Notifications are paired to real-time mindfulness based interventions.
Primary Outcome Measure Information:
Title
Number of participants with return to drug use
Description
Relapse to use of substance use defined as 1) self-reported use, 2) positive urine drug screen (from treatment program) or 3) provider report of confirmed relapse (Only applies to substances for which subject is receiving treatment)
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of participants retained in treatment
Description
Participants status as engaged in recovery treatment (index treatment program or other)
Time Frame
3 months
Title
Number of hospitalizations and emergency department visits per participant
Description
Includes absolute number of Emergency Department visits (SUD and non-SUD related), number of unplanned hospital admissions (SUD and non-SUD related), number of days hospitalized (SUD and non-SUD related admissions) and overdose related visits
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years or older Enrolled in an outpatient SUD treatment program Enrolled in treatment for < 90 days Fluent in English Have access to a smartphone with iOS or Android Capabilities Capable of providing informed consent Exclusion Criteria: Pregnancy Prisoner Status Significant limitation of range of motion of non-dominant arm (amputation or fracture)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephanie Carreiro, MD
Phone
5084211400
Email
stephanie.carreiro@umassmed.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Melissa Taylor, BS
Email
melissa.taylor@umassmed.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Megan Reinhardt
Organizational Affiliation
ContinueYou, LLC
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Massachusetts Chan Medical School
City
Worcester
State/Province
Massachusetts
ZIP/Postal Code
01655
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stephanie Carreiro, MD
Email
stephanie.carreiro@umassmed.edu
First Name & Middle Initial & Last Name & Degree
Stephanie Carreiro, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33748430
Citation
Carreiro S, Taylor M, Shrestha S, Reinhardt M, Gilbertson N, Indic P. Realize, Analyze, Engage (RAE): A Digital Tool to Support Recovery from Substance Use Disorder. J Psychiatr Brain Sci. 2021;6:e210002. doi: 10.20900/jpbs.20210002. Epub 2021 Feb 24.
Results Reference
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PubMed Identifier
32193048
Citation
Carreiro S, Chintha KK, Shrestha S, Chapman B, Smelson D, Indic P. Wearable sensor-based detection of stress and craving in patients during treatment for substance use disorder: A mixed methods pilot study. Drug Alcohol Depend. 2020 Apr 1;209:107929. doi: 10.1016/j.drugalcdep.2020.107929. Epub 2020 Mar 3.
Results Reference
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RAE (Realize, Analyze, Engage)

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