N/A
N=47
Chronic Care Management/Patient Relationship Management Proof of Concept
Diabetes Mellitus
Bottom Line
View on ClinicalTrials.gov: NCT01182480 ↗Enrolled (actual)
47
Serious AEs
0.0%
Results posted
Nov 2014
Primary outcome: Primary: Patient Engagement — 68.14 text message response rate (percent)
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Patient Relationship Management (PRM) Program (Behavioral)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Denver Health and Hospital Authority
- Primary completion
- Mar 2011
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Patient Engagement |
68.14 | — |
| SECONDARY Appointment Attendance |
— | — |
| SECONDARY Perceived Self-efficacy |
— | — |
| SECONDARY Glycemic Control |
— | — |
Summary
This proof of concept study proposes to evaluate the feasibility of a communications-technology-based chronic care and patient relationship management program to improve diabetes self management among adult diabetic patients in an urban safety net population by providing between-visit reminders and chronic disease support through cell phone text messaging.
The investigators hypothesize that diabetic patients enrolled in the program will be less likely to miss scheduled appointments and will have greater perceived self-efficacy and improved patient satisfaction concerning chronic disease management. No-show rates among patients enrolled in the program are expected to be lower than among patients receiving standard care.
Eligibility Criteria
Inclusion Criteria
- patients with diabetes
- receive care at a primary care clinic in the DH system
- between 18 and 76 years of age
- primary language of English or Spanish
- ownership of a qualifying cell phone (SMS text capable)
- ownership of a glucometer.
Exclusion Criteria
- life expectancy less than six months,
- do not have or cannot use a phone or glucometer
- do not want to participate
Data sourced from ClinicalTrials.gov (NCT01182480). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.