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Developing Affective HeaLth to Improve Adherence to Health Behaviors in Diabetes (DAHLIA II)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Happify
Sponsored by
Happify Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diabetes Mellitus, Type 2

Eligibility Criteria

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

Inclusion Criteria:

  • Adults with Type 2 Diabetes
  • Elevated HbA1c levels (7 or greater)
  • No prior experience on the Happify platform (new user registration)
  • PHQ-8 score of 13 or higher
  • US resident
  • Under the care of a medical professional for the treatment of their diabetes
  • Be willing and able to obtain HbA1c every 3 months

Exclusion Criteria:

  • none

Sites / Locations

  • Happify (an online platform -- study is entirely online)

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Positive affect condition

Psychoeducation condition

Arm Description

Participants use Happify and have the option to use a diabetes-specific track that focuses on building skills for greater happiness, reducing stress, and coping better with diabetes. Users may access a wide variety of 4-week programs and use them in any way they desire for the entire study period.

Participants complete a series of quizzes and polls on Happify designed to engage them in thinking about well-being topics, but without giving any specific instructions for how to promote well-being. Participants gain access to 8 weeks worth of content, but may repeat the content as often as they like in the follow-up period.

Outcomes

Primary Outcome Measures

Change in self-reported HbA1C level
1-item self-reported measure of Hemoglobin A1C (HbA1C) level, "What was your most recent HbA1c level?"

Secondary Outcome Measures

Change in Depression symptoms [PHQ-9 questionnaire]
9-item measure of depressive symptoms scoring how often the participant has been bothered by each statement over the past 2 weeks from not at all (0) to nearly every day (3).
Change in Diabetes Regimen Adherence
1-item measure on keeping up with diabetes regimen in the past 24 hours, asking "Which of the following activities in your diabetes regimen did you complete over the past 24 hours?"
Change in Perceived Stress [Perceived Stress Scale (PSS)]
10-item measure of perceived stress scoring how often the participant felt stressed by each statement in the following month from never (0) to very often (4).
Change in diabetes self-care activities [Summary of Diabetes Self-Care Activities (SDSCA)]
11-item measure of self-reported adherence to diabetes self-care activities, ex. "On how many of the last seven days did you participate in at least 30 minutes of physical activity?" with possible answers of 0 to 7 days for each question.
Change in positive affect [Patient-Reported Outcomes Measurement Information Systems - Positive Affect Subscale(PROMIS)]
15-item measure of positive affect scoring participants on how often then felt each statement was true over the past 7 days from not at all (1) to very much (5)

Full Information

First Posted
August 23, 2019
Last Updated
July 15, 2022
Sponsor
Happify Inc.
Collaborators
Northwestern University
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1. Study Identification

Unique Protocol Identification Number
NCT04068805
Brief Title
Developing Affective HeaLth to Improve Adherence to Health Behaviors in Diabetes (DAHLIA II)
Official Title
Developing Affective HeaLth to Improve Adherence to Health Behaviors in Diabetes (DAHLIA II)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Terminated
Why Stopped
The Sponsor chose to terminate this study for commercial reasons.
Study Start Date
August 31, 2020 (Actual)
Primary Completion Date
April 1, 2021 (Actual)
Study Completion Date
July 12, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Happify Inc.
Collaborators
Northwestern University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Participants will be randomly assigned to either a positive affect skills intervention or a psychoeducation control group and assessed with questionnaires before, during, and after the 8-week program, as well as at 3 months, 6 months, and 12 months after the end of the program.
Detailed Description
Participants will be randomly assigned to either the Diabetes positive affect skills intervention or a psychoeducation control group. Both programs last 8 weeks and take place on a simplified research version of the Happify platform. Participants assigned to the diabetes positive affect program will have full access to Happify, with a track that focuses on building skills for greater happiness, reducing stress, and coping better with diabetes displayed as the feature track. Participants assigned to the psychoeducation (control) condition will be asked to complete a series of polls on various wellbeing topics, and then provided with some social comparison data about how their responses compared with the responses of other users, as well as information about why the well being topic is important. Participants will be asked to complete questionnaires before, during, and after the 8-week program as well as 3 months, 6 months and 12 months follow-up questionnaires after the program is complete, at which point study participation will end.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Users are randomly assigned between arms after completing baseline assessment and stay in that arm for the duration of the study.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Positive affect condition
Arm Type
Active Comparator
Arm Description
Participants use Happify and have the option to use a diabetes-specific track that focuses on building skills for greater happiness, reducing stress, and coping better with diabetes. Users may access a wide variety of 4-week programs and use them in any way they desire for the entire study period.
Arm Title
Psychoeducation condition
Arm Type
Sham Comparator
Arm Description
Participants complete a series of quizzes and polls on Happify designed to engage them in thinking about well-being topics, but without giving any specific instructions for how to promote well-being. Participants gain access to 8 weeks worth of content, but may repeat the content as often as they like in the follow-up period.
Intervention Type
Behavioral
Intervention Name(s)
Happify
Intervention Description
An online platform for conveying techniques from positive psychology, cognitive-behavioral therapy, and mindfulness-based stress reduction.
Primary Outcome Measure Information:
Title
Change in self-reported HbA1C level
Description
1-item self-reported measure of Hemoglobin A1C (HbA1C) level, "What was your most recent HbA1c level?"
Time Frame
Baseline, 3 weeks post-intervention (day 83), 3 weeks after 3-month post intervention (day 173), 3 weeks after 6 month post intervention (day 263), and 12 months post intervention (day 416)
Secondary Outcome Measure Information:
Title
Change in Depression symptoms [PHQ-9 questionnaire]
Description
9-item measure of depressive symptoms scoring how often the participant has been bothered by each statement over the past 2 weeks from not at all (0) to nearly every day (3).
Time Frame
Baseline, immediate post-intervention at 8 weeks, and at 3, 6, and 12 months post-intervention
Title
Change in Diabetes Regimen Adherence
Description
1-item measure on keeping up with diabetes regimen in the past 24 hours, asking "Which of the following activities in your diabetes regimen did you complete over the past 24 hours?"
Time Frame
From baseline up to 63 days, 7 days at 3 months post intervention (146-153), 7 days at 6 months post intervention (236-243), and 12 months post intervention (day 416-423)
Title
Change in Perceived Stress [Perceived Stress Scale (PSS)]
Description
10-item measure of perceived stress scoring how often the participant felt stressed by each statement in the following month from never (0) to very often (4).
Time Frame
Baseline, immediate post-intervention at 8 weeks, and at 3, 6, and 12 months post-intervention
Title
Change in diabetes self-care activities [Summary of Diabetes Self-Care Activities (SDSCA)]
Description
11-item measure of self-reported adherence to diabetes self-care activities, ex. "On how many of the last seven days did you participate in at least 30 minutes of physical activity?" with possible answers of 0 to 7 days for each question.
Time Frame
Baseline, immediate post-intervention at 8 weeks, and at 3, 6, and 12 months post-intervention
Title
Change in positive affect [Patient-Reported Outcomes Measurement Information Systems - Positive Affect Subscale(PROMIS)]
Description
15-item measure of positive affect scoring participants on how often then felt each statement was true over the past 7 days from not at all (1) to very much (5)
Time Frame
Baseline, immediate post-intervention at 8 weeks, and at 3, 6, and 12 months post-intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults with Type 2 Diabetes Elevated HbA1c levels (7 or greater) No prior experience on the Happify platform (new user registration) PHQ-8 score of 13 or higher US resident Under the care of a medical professional for the treatment of their diabetes Be willing and able to obtain HbA1c every 3 months Exclusion Criteria: none
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eliane Boucher, PhD
Organizational Affiliation
Happify Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
Happify (an online platform -- study is entirely online)
City
New York
State/Province
New York
ZIP/Postal Code
10012
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32749998
Citation
Boucher E, Moskowitz JT, Kackloudis GM, Stafford JL, Kwok I, Parks AC. Immediate and Long-Term Effects of an 8-Week Digital Mental Health Intervention on Adults With Poorly Managed Type 2 Diabetes: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2020 Aug 4;9(8):e18578. doi: 10.2196/18578.
Results Reference
derived

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Developing Affective HeaLth to Improve Adherence to Health Behaviors in Diabetes (DAHLIA II)

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