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Improving Physical Activity Through a mHealth Intervention in Cardio-metabolic Risk Patients

Primary Purpose

Diabetes Mellitus, Type 2, Prediabetic State, Hypertension

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
FeatForward App (on study smartphone)
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetes Mellitus, Type 2

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥18 years old
  • Diagnosis of any of the following: pre-diabetes, Type 2 Diabetes Mellitus (T2DM), pre-hypertension, hypertension, and/or obesity (Body Mass Index (BMI) ≥ 30 kg/m2).

    • T2DM: Glycated Hemoglobin (HbA1c) >7.0%
    • Hypertension: Blood Pressure (BP) of 140/90 mmHg
    • Pre-diabetes: HbA1c >5.7% and BMI ≥ 25 kg/m2
    • Pre-hypertension: BP of 130/90 mmHg and family history of high BP
  • Willingness to attend all 3 study visits
  • Ability to read and speak fluent English
  • Physical independence (i.e., ability to walk without assistance)
  • Ability to consent for oneself
  • Willingness to switch to a provided Samsung smartphone and appropriate phone plan to use as a primary phone for the 6-month study duration
  • Willingness to wear a Samsung smartwatch during all hours excluding sleep for the duration of the study

Exclusion Criteria:

  • Participants with severe depression assessed by scoring ≥20 on the PHQ-8 screening questionnaire for depression
  • Self-reported eating disorder and/or other psychiatric disorders
  • Current or recent participation (within 3 months) in a weight loss program
  • Prior or planned bariatric surgery procedure
  • Use of medications known to cause significant (≥ 5%) long-term changes in body weight or BP
  • Pregnancy or plans to get pregnant within 6 months of enrollment
  • Disability, dementia or neurological deficits, and other medical or surgical conditions preventing participants from engaging in self-care
  • Serious co-morbid conditions (e.g., terminal cancers, end-stage renal disease) that preclude safe participation in moderate levels of physical activity, under discretion of the participants' primary care provider

Sites / Locations

  • Mass General: Charlestown Healthcare Center
  • Mass General Revere HealthCare Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Group A

Group B

Arm Description

Receive a Samsung smartphone Receive the FeatForward app Receive a Samsung smartwatch Continue to receive medical care as usual

Receive a Samsung smartphone Receive a Samsung smartwatch Continue to receive medical care as usual

Outcomes

Primary Outcome Measures

Differences in the change in physical activity levels between control and intervention groups as measured by daily physical activity measured by the Gear Fit device provided to participants in both groups

Secondary Outcome Measures

Differences in the change in body weight between control and intervention groups
Differences in the change in HbA1c between control and intervention groups
Differences in the change in fasting blood glucose between control and intervention groups
Differences in the change in blood pressure between control and intervention groups
Differences in the change in waist circumference between control and intervention groups
Differences in the change in serum lipids between control and intervention groups
Differences in the change in C-reactive protein between control and intervention groups

Full Information

First Posted
September 10, 2015
Last Updated
August 29, 2020
Sponsor
Massachusetts General Hospital
Collaborators
Samsung Electronics
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1. Study Identification

Unique Protocol Identification Number
NCT02551640
Brief Title
Improving Physical Activity Through a mHealth Intervention in Cardio-metabolic Risk Patients
Official Title
Improving Physical Activity Behavior in Patients With High Cardio-metabolic Risk Using a Multi-modal mHealth Intervention: a 2-arm Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
September 2015 (Actual)
Primary Completion Date
April 2018 (Actual)
Study Completion Date
December 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
Collaborators
Samsung Electronics

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to explore the effects of FeatForward on physical activity and cardio-metabolic risk factors. The study will be implemented as a 2-arm randomized controlled trial (RCT) comparing the effects of FeatForward in patients assigned to use the application versus a control group who will not use the app over a 6-month follow-up period. The investigators hypothesize that subjects using FeatForward will be more physically active and will achieve greater improvements in their cardio-metabolic risk (CMR) factors than a usual care control group that will not use the app over a 6-month period.
Detailed Description
TextToMove (TTM) was a dynamic text messaging program which the investigators developed in 2012 with the goals of increasing physical activity in patients with type 2 diabetes mellitus (T2DM), improving self-management of the disease, and lowering HbA1c levels. TTM has since been evaluated in a PHRC-approved randomized controlled trial. In our current proposed study, the investigators plan to convert TTM into a mobile application for smartphone use, with increased and improved functionality and with the potential for easy translation to additional use cases. The investigators used feedback gathered from users and observations from the previous trial to shape the development plan for this second iteration, aptly named "FeatForward." The FeatForward app will be hyper-personalized to users and to respond specifically to individual users' behavior patterns so that the application feels like an intelligent health coach partnering with users to achieve better health outcomes. What defines FeatForward from TTM are additional features, including the incorporation of machine learning components for the messaging algorithm, tailoring of message frequency based on users' activity levels, integration of patient data into the electronic medical records through the Remote Monitoring Data Repository, inputs to improve the generalizability of feedback regarding health metrics (e.g., weight, blood glucose), as well as a community feature to enable interactions with other similar patients and a comprehensive educational library. FeatForward's primary goal is to help users increase their level of physical activity. Physical inactivity has been identified as one of the leading risk factors contributing to the rising rates of chronic diseases. And despite being the most common cardio-metabolic risk (CMR) factor, it also happens to be the easiest to target. Current estimates suggest that over half (52%) of adults in the United States do not meet the recommended physical activity levels. A number of studies to date have demonstrated the dose-response protective effect of increasing physical activity on the development of diabetes and cardiovascular disease. Therefore, the investigators hypothesize that FeatForward will help users to increase their physical activity levels and also lead to improvements in cardio-metabolic risk factors compared to usual care controls that will not use the intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Prediabetic State, Hypertension, Prehypertension, Obesity

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
300 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Group A
Arm Type
Experimental
Arm Description
Receive a Samsung smartphone Receive the FeatForward app Receive a Samsung smartwatch Continue to receive medical care as usual
Arm Title
Group B
Arm Type
No Intervention
Arm Description
Receive a Samsung smartphone Receive a Samsung smartwatch Continue to receive medical care as usual
Intervention Type
Other
Intervention Name(s)
FeatForward App (on study smartphone)
Intervention Description
The FeatForward mobile app will have the following features: Messaging: Educational messages tailored to user's medical conditions and motivational messages tailored to user's stage of change. Tracking: Ability to track physical activity, weight, blood pressure, blood glucose and heart rate. Community: Users in later stages of change able to encourage and motivate one another through groups. Educational Library: To provide educational tips and health information. Provider Engagement: Ability for physicians to view patient data, and send messages to patients. Monthly depression assessments: The app will prompt users to complete a monthly voluntary depression assessment. Social Support: Those using the FeatForward app will also have access to a Facebook group.
Primary Outcome Measure Information:
Title
Differences in the change in physical activity levels between control and intervention groups as measured by daily physical activity measured by the Gear Fit device provided to participants in both groups
Time Frame
3 & 6 months
Secondary Outcome Measure Information:
Title
Differences in the change in body weight between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in HbA1c between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in fasting blood glucose between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in blood pressure between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in waist circumference between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in serum lipids between control and intervention groups
Time Frame
3 & 6 months
Title
Differences in the change in C-reactive protein between control and intervention groups
Time Frame
3 & 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥18 years old Diagnosis of any of the following: pre-diabetes, Type 2 Diabetes Mellitus (T2DM), pre-hypertension, hypertension, and/or obesity (Body Mass Index (BMI) ≥ 30 kg/m2). T2DM: Glycated Hemoglobin (HbA1c) >7.0% Hypertension: Blood Pressure (BP) of 140/90 mmHg Pre-diabetes: HbA1c >5.7% and BMI ≥ 25 kg/m2 Pre-hypertension: BP of 130/90 mmHg and family history of high BP Willingness to attend all 3 study visits Ability to read and speak fluent English Physical independence (i.e., ability to walk without assistance) Ability to consent for oneself Willingness to switch to a provided Samsung smartphone and appropriate phone plan to use as a primary phone for the 6-month study duration Willingness to wear a Samsung smartwatch during all hours excluding sleep for the duration of the study Exclusion Criteria: Participants with severe depression assessed by scoring ≥20 on the PHQ-8 screening questionnaire for depression Self-reported eating disorder and/or other psychiatric disorders Current or recent participation (within 3 months) in a weight loss program Prior or planned bariatric surgery procedure Use of medications known to cause significant (≥ 5%) long-term changes in body weight or BP Pregnancy or plans to get pregnant within 6 months of enrollment Disability, dementia or neurological deficits, and other medical or surgical conditions preventing participants from engaging in self-care Serious co-morbid conditions (e.g., terminal cancers, end-stage renal disease) that preclude safe participation in moderate levels of physical activity, under discretion of the participants' primary care provider
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kamal Jethwani, MD, MPH
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mass General: Charlestown Healthcare Center
City
Charlestown
State/Province
Massachusetts
ZIP/Postal Code
02129
Country
United States
Facility Name
Mass General Revere HealthCare Center
City
Revere
State/Province
Massachusetts
ZIP/Postal Code
02151
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
11427773
Citation
Kohl HW 3rd. Physical activity and cardiovascular disease: evidence for a dose response. Med Sci Sports Exerc. 2001 Jun;33(6 Suppl):S472-83; discussion S493-4. doi: 10.1097/00005768-200106001-00017.
Results Reference
background
PubMed Identifier
11427776
Citation
Kelley DE, Goodpaster BH. Effects of exercise on glucose homeostasis in Type 2 diabetes mellitus. Med Sci Sports Exerc. 2001 Jun;33(6 Suppl):S495-501; discussion S528-9. doi: 10.1097/00005768-200106001-00020.
Results Reference
background

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Improving Physical Activity Through a mHealth Intervention in Cardio-metabolic Risk Patients

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