- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03487692
Medical Care, Education, Social Support, And Goal-setting to Empower Self-management for Diabetes (MESSAGES)
November 1, 2022 updated by: University of Chicago
Diabetes MESSAGES (Medical Care, Education, Social Support, And Goal-setting to Empower Self-management): Implementing Diabetes Group Visits and Text Messaging in Community Health Centers
Diabetes group visits, shared appointments where patients receive self-management education in a group setting and have a medical visit, are a promising way to deliver high quality diabetes care.
Group visits can improve glycemic control and decrease healthcare utilization.
To date, no studies have systematically implemented a diabetes group visit intervention in a network of U.S. community health centers.
The University of Chicago is partnering with Midwest Clinicians' Network (MWCN), a member organization of 130 health centers across ten Midwestern states.
Approximately half of all Federally Qualified Health Centers in this region are affiliated with MWCN.
The objectives of the study are [1] providers and staff at 20 health centers will have the requisite knowledge, skills, and motivation to implement a diabetes group visit plus text messaging intervention at their sites; [2] changes in diabetes processes of care; knowledge, attitudes, and skills for diabetes self-management; clinical outcomes; and health care utilization for patients participating in the diabetes group visit program will be evaluated; and [3] the diabetes group visit program will be available for dissemination among and use by health centers and healthcare providers at the local, state, regional, and national levels.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
UChicago and MWCN will recruit and enroll 20 health centers (HCs) to participate in a training intervention and to implement diabetes group visit and text messaging programs at their clinic sites.
Each HC will assemble a team of 3-4 providers and staff to participate in the training.
HCs will be randomized to one of two training cohorts.
HC providers and staff will attend two in-person Learning Sessions in Chicago and a series of monthly webinars, recruit and enroll patients, implement a 6-month diabetes group visit and text messaging program plus subsequent booster sessions, complete periodic surveys and interviews, assist with data collection through patient surveys and chart abstraction, and present their program to peer HCs during Learning Sessions and to local stakeholders, state primary care organizations, or other professional groups.
Each HC will enroll 15 patients in the group visit and text messaging program; the 2018 Training Cohort will do so immediately following their enrollment in the study and the 2020 Training Cohort will do so after 18 months.
During the first 18 months, the 2020 Training Cohort will collect data from electronic health records (EHR) of randomly selected patients to serve as a control group.
Changes in self-reported outcomes, diabetes processes of care, and clinical outcomes will be assessed for intervention patients from baseline through 2 year follow up, and processes of care and clinical outcomes will be compared for intervention vs. control participants.
Capacity of HC providers and staff to conduct a group visit and text messaging intervention for patients with diabetes, as well as their confidence in identifying and addressing health disparities, will be evaluated through surveys and in-depth interviews.
This study will expand knowledge of the barriers, facilitators, and perceived benefits and drawbacks of group visit and text messaging interventions and inform the development of a toolkit that will be disseminated to other HCs.
Study Type
Interventional
Enrollment (Actual)
265
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Illinois
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Chicago, Illinois, United States, 60637
- University of Chicago
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years or older
- diagnosis of type 2 diabetes
- attended at least two appointments at the HC within the past year, with at least one of them being during the past six months
- last documented A1c result greater than or equal to 8.0% (test must have been done during the last 6 months)
- own a cellular phone with text messaging capabilities
- have the ability to read and send text messages
- English or Spanish speaking
Exclusion Criteria:
- pregnant or planning to become pregnant
- uncontrolled psychiatric problem
- dementia or other cognitive impairment
- hearing difficulties or severe physical disability that would prevent them from participation in group visit
- planning to relocate in the next year or leave the area during the group visit period
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: 2018 Training Cohort
10 health centers will be randomized to the 2018 Training Cohort.
Teams from these health centers will be trained and will implement a 6 month diabetes group visit and text messaging intervention (Diabetes MESSAGES Program).
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Health centers in the 2018 Training Cohort will enroll groups of 10-15 patients to attend 6 monthly diabetes group visits consisting of group education, social support, goal setting, and an individual medical visit for each patient.
At the same time, patients will be enrolled in a 6-month interactive diabetes text messaging program.
Patients will receive quarterly booster sessions for 1-2 years after the 6-month intervention period.
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Other: 2020 Training Cohort
10 health centers will be randomized to the 2020 Training Cohort.
Prior to beginning training, these health centers will collect data on randomly selected patients receiving usual care to serve as the control group.
After this first parallel group trial period, teams from these health centers will be trained and will implement the 6 month diabetes group visit and text messaging intervention during a second single group trial period (Diabetes MESSAGES Program (second trial)).
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During the first trial period, health centers in the 2020 Training Cohort will collect data on patients receiving usual care.
After the first trial period, health centers in the 2020 Training Cohort will enroll groups of 10-15 patients to attend 6 monthly diabetes group visits consisting of group education, social support, goal setting, and an individual medical visit for each patient.
At the same time, patients will be enrolled in a 6-month interactive diabetes text messaging program.
Patients will receive quarterly booster sessions for 1-2 years after the 6-month intervention period.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Hemoglobin A1C
Time Frame: change from baseline to 12 months
|
change from baseline to 12 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Hemoglobin A1C
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
|
Blood pressure
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
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Weight
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
|
Cholesterol
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
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Diabetes processes of care
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
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Receipt of recommended screenings, exams, referrals, and vaccinations
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
Medication management of diabetes
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
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changes in prescribed diabetes medications for patients with inadequate diabetes control
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baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
Number of hypoglycemic events
Time Frame: baseline, 6 month, and 12 month for intervention patients only
|
baseline, 6 month, and 12 month for intervention patients only
|
|
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Number of hospital admissions
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
|
Number of primary care, specialist, and ER visits
Time Frame: baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
baseline, 6 month, and 18 month for intervention vs. control patients; 30 month for intervention patients only
|
|
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Smoking status
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
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|
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Health related quality of life (SF-12)
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
|
|
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Depression (PHQ-2)
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
|
|
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Summary of Diabetes Self-Care Activities Measure
Time Frame: baseline, 6 month, and 12 month for intervention patients only
|
baseline, 6 month, and 12 month for intervention patients only
|
|
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Understanding of Diabetes Self-Management (Diabetes Care Profile)
Time Frame: baseline, 6 month, and 12 month for intervention patients only
|
baseline, 6 month, and 12 month for intervention patients only
|
|
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Attitudes Towards Diabetes (Diabetes Care Profile)
Time Frame: baseline, 6 month, and 12 month for intervention patients only
|
baseline, 6 month, and 12 month for intervention patients only
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|
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Diabetes Distress Scale (DDS-2)
Time Frame: baseline, 6 month, and 12 month for intervention patients only
|
baseline, 6 month, and 12 month for intervention patients only
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|
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Diabetes Quality of Life Scale
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
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|
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Diabetes Self-Empowerment Scale
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
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|
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Diabetes Social Support Scale
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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baseline, 6 month, and 12 month for intervention patients only
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|
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Patient satisfaction with intervention
Time Frame: 6 month and 12 month for intervention patients only
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6 month and 12 month for intervention patients only
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CAHPS Overall Rating
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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Patient satisfaction with overall care at health center
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baseline, 6 month, and 12 month for intervention patients only
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CAHPS Cultural Competency
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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Patient satisfaction with cultural competency of care at health center
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baseline, 6 month, and 12 month for intervention patients only
|
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CAHPS Provider Communication
Time Frame: baseline, 6 month, and 12 month for intervention patients only
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Patient satisfaction with provider communication at health center
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baseline, 6 month, and 12 month for intervention patients only
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Patient engagement
Time Frame: through study completion, an average of 2 years
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Attendance/participation in group visits, text messaging, and booster sessions
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through study completion, an average of 2 years
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Health center provider/staff preparedness
Time Frame: change from pre- to post-training (from baseline to 1 month, 7 month, and 16 month)
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Capacity, confidence, motivation, perceived benefits and barriers
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change from pre- to post-training (from baseline to 1 month, 7 month, and 16 month)
|
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Health center provider/staff satisfaction
Time Frame: post-training (16 month)
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Satisfaction with training, group visits, and text messaging
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post-training (16 month)
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Arshiya Baig, MD, MPH, University of Chicago
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 18, 2018
Primary Completion (Actual)
May 15, 2022
Study Completion (Actual)
June 30, 2022
Study Registration Dates
First Submitted
March 21, 2018
First Submitted That Met QC Criteria
March 27, 2018
First Posted (Actual)
April 4, 2018
Study Record Updates
Last Update Posted (Actual)
November 3, 2022
Last Update Submitted That Met QC Criteria
November 1, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IRB17-1385
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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