Reaching Better Health Study: A Website to Improve Type 2 Diabetes Self-Management

NCT ID: NCT02757937

Last Updated: 2018-12-17

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 513 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-05-31
• Study Completion Date: 2017-12-31

Brief Summary

Diabetes is one of the most common chronic illnesses among adults in the United States. Internet-based interventions and health promotion websites for patients with Type 2 Diabetes are typically low-cost, easily accessible, and attractive. The purpose of this study is to determine whether participants' utilization of a health & wellness website focused on diabetes self-management increases participants' self-reported self-efficacy toward managing their Type 2 Diabetes through behavior change and self-reported medication adherence compared to standard care.

Detailed Description

Diabetes is one of the most common chronic illnesses among adults in the United States. Merck & Co., Inc. has produced an innovative website to engage adult patients in chronic illness self-management and medication adherence. Internet-based interventions and health promotion websites for patients are typically low-cost, easily accessible, and attractive. However, there is a growing need for improved measurement, implementation and evaluation of online health interventions to ensure patient engagement and produce more significant behavior change that can impact patients' health over the long term.

The primary objective of this study is to determine whether utilization of the health and wellness website increases participants' self-reported self-efficacy toward managing their Type 2 Diabetes through behavior change and self-reported medication adherence.

This study comprises a randomized controlled trial utilizing the website as the self-management support intervention. There is no interventional medical treatment, and no change in patients' medical care. In collaboration with University of Pennsylvania, potential participants will be identified and recruited from the Penn Medicine outpatient population based on specific inclusion/exclusion criteria. Participants will remain in the study for 6 months.

Participants will be randomly assigned to the intervention or control condition (no exposure). Those in the intervention arm will have access to health & wellness website for nine months post enrollment. Online surveys will be delivered during this nine month period. Primary outcomes will be baseline-to-two month and baseline-to-4 month changes in diabetes management self-efficacy scores as measured by the Diabetes Self-Efficacy Scale.

Conditions

Diabetes Mellitus, Type 2

Keywords

Medication Adherence; Self-efficacy; Behavior; Diabetes; Diabetes Mellitus

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Health & Wellness Website

Subjects will receive access to an interactive health \& wellness website for 6 months. The site aims to provide patients with information, tools, and resources to manage their chronic condition (e.g., Type 2 diabetes). The website will send subjects emails with tips to help them take better care of their diabetes, such as how to track diet and exercise habits and how to cook healthy meals. The study researchers will keep track of how many times subjects access the website and which parts of the site are most commonly viewed. Intervention subjects will receive questionnaires assessing engagement and satisfaction with the website. Subjects will also complete questionnaires at baseline and 2, 4, and 6 months post-baseline.

Group Type: EXPERIMENTAL

Health & Wellness Website

Intervention Type: BEHAVIORAL

Educational website for patients with chronic disease (i.e., Type 2 diabetes, asthma, high blood pressure, high cholesterol). The website is a free interactive resource to help patients manage their health condition(s) each day and to help them achieve their goals. It is a multichannel health and wellness platform to help patients adhere to their treatment and care plans between office visits.

Control Arm

Subjects in the control arm will continue with standard diabetes care without getting access to the intervention website. Subjects will also complete questionnaires at baseline and 2, 4, and 6 months post-baseline. Control subjects will be granted access to the health \& wellness website after the study is completed.

Group Type: OTHER

Control Arm

Intervention Type: OTHER

Continue with standard diabetes care without getting access to the intervention website.

Interventions

Health & Wellness Website

Educational website for patients with chronic disease (i.e., Type 2 diabetes, asthma, high blood pressure, high cholesterol). The website is a free interactive resource to help patients manage their health condition(s) each day and to help them achieve their goals. It is a multichannel health and wellness platform to help patients adhere to their treatment and care plans between office visits.

Intervention Type: BEHAVIORAL

Control Arm

Continue with standard diabetes care without getting access to the intervention website.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patient is a current patient in the Penn Medicine outpatient healthcare system
• Patient's Primary Care Physician (PCP) or Endocrinologist is a Penn Medicine provider
• Patient has a 12 month history of healthcare utilization in the Penn Medicine system (in-office PCP/endocrinologist visits)
• Patient has complete data (ICD-10 code for Type 2 diabetes diagnosis, date of diagnosis, name and mailing address information) in the Penn Data Warehouse
• Patient is diagnosed with Type II Diabetes as indicated by ICD-10 Codes: E11.** (including any newly diagnosed)
• Patients' HbA1c was ≥8.0% in last 6 months (if more than one A1c result present in record, most recent measurement assessed)
• Patient can read and understand English well enough to complete study tasks.
• Patient has regular access to a telephone
• Patient has at least bi-weekly access to internet and email
• Patient agrees to release their medical record information to Children's Hospital of Philadelphia research team

Exclusion Criteria

• Patient is deceased
• Patient has indicated "Do Not Solicit for Research" in medical record
• Patient is less than 18 years of age
• Patient is older than 75 years old
• Patient uses an insulin pump or injectable insulin to treat/manage their diabetes.
• Patient is non-English speaking
• Patient does not have HbA1c% in chart from last 6 months
• Patients' HbA1c in last 6 months is <8.0%
• Patient is currently taking medications that can raise glucose levels, such as steroids
• Patient has a history of cognitive disorders, mental illness, and/or cognitive impairment that may impact their ability to use an online website, including, dementia, Alzheimer's disease, Parkinson's disease, traumatic brain or head injury, and psychosis
• Patient has history of Heart Failure (included Chronic Heart Disease, Chronic Heart Failure) and/or Chronic Kidney Disease, and has had other serious cardiovascular conditions (e.g, heart attack or stroke) in the last 6 months
• Patient has history of endocrine gland cancers or pancreatic cancers
• Patient is undergoing chemotherapy or immunotherapy treatment in last 6 months
• Patient's medical record contains ICD-10 Code for Type I diabetes diagnosis.
• Patient's medical record contains ICD-10 Code for pregnancy-related diabetes:

• 024.419 (gestational diabetes)
• 024.419 (antepartum gestational diabetes)
• Z79.4 (type II long term insulin use)
• 024.91x (pregnant women who are diabetic)
• Patient is Pre-diabetic or borderline Type 2 diabetic
• Patient is pregnant or lactating
• Patient's electronic medical history data is not available through Penn Medicine's electronic medical record and/or is not complete in Penn Data Store
• Patients who, in the opinion of the Investigator, may be non-compliant with study schedules or procedures

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role: collaborator

University of Pennsylvania

OTHER

Sponsor Role: collaborator

Children's Hospital of Philadelphia

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Linda Fleisher, PhD, MPH

Role: PRINCIPAL_INVESTIGATOR

Children's Hospital of Philadelphia

Other Identifiers

15-011892

Identifier Type: -

Identifier Source: org_study_id