NCT05555095 · OSF Healthcare System
Examining Digital Health Care Delivery Models Through Medicaid Collaborative
(MIC)
What this study is about
The purpose of this study is to examine the intervention effectiveness and dissemination of digital health care delivery models for improving selected health outcomes in the Medicaid population.
View original scientific description
The purpose of this study is to examine the intervention effectiveness and dissemination of digital health care delivery models for improving selected health outcomes in the Medicaid population.
Interventions
BEHAVIORAL
digital health delivered multicomponent intervention
The MIC program will have set minimum levels of connectivity for each of the three defined conditions under study.
Primary outcome measures
Change in participant's blood pressure control at three points in time
Time frame: 3 months, 6 months, 12 months
Decrease in the average systolic and/or diastolic blood pressure
Change in participant's glycemic control at three points in time
Time frame: 3 months, 6 months, 12 months
Defined as a reduction \>1% in glycosylated hemoglobin (hemoglobin A1C)
Change in Patient Assessment of Chronic Illness Care scale (PACIC) from baseline to exit from program
Time frame: baseline, end of program, on average of 1 year
Measure of patient's perception of care management for chronic disease - 20 items on a 5-point scale 1=no or never to 5=Always, with higher score indicating better care
Change in Patient Perception of Health Care Management (adapted form of PACIC to reflect pre/postnatal care) from baseline to exit from program
Time frame: baseline, end of program, on average 6 months
Measure of patient-centered care and self-management - 20 items on a 5-point scale 1=no or never to 5=Always, with higher score indicating better care
Patient satisfaction, 1-item researcher generated question
Time frame: at exit from program, on average 1 year
Measure of patient's satisfaction, Participant's recommendation of program to others (Yes/No)
Who can participate
This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.
Inclusion criteria
- Patient of one of four medically qualified health care centers and/or OSF HealthCare as defined by insurance type
- Insured by Medicaid or dually eligible for Medicare or Medicaid
- Has one or more of the three following conditions: Hypertension, Diabetes Mellitus, or Pregnancy
- Able to read and understand English or read translated materials in language provided (e.g. Spanish)
- Minors who are pregnant and less 18 years of age who are enrolled in the MIC Program
Exclusion criteria
- Not enrolled in the MIC Program
- No one will be excluded on basis of sex or race
Where
- Peoria, Illinois
Related conditions & keywords
Frequently asked questions
What is a clinical trial?
A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.
Is it safe to participate?
Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.
Will I be compensated?
Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.
Will I receive a placebo instead of treatment?
When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.
Can I leave a trial if I change my mind?
Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.
How long does a clinical trial last?
Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.
Data: ClinicalTrials.gov · synced Apr 30, 2025 · Source of record for eligibility and locations