Trial Outcomes & Findings for Chronic Care Management/Patient Relationship Management Proof of Concept (NCT NCT01182480)
NCT ID: NCT01182480
Last Updated: 2014-11-05
Results Overview
Patient engagement was assessed by patient text message response rates and average response times. Response rates were calculated as a percentage from the number of patient-initiated text messages sent in response to a system-generated request for information (the numerator) divided by the total number of system-generated requests for information (the denominator). Average response times were calculated from system-recorded time stamps for outbound requests sent and inbound patient-initiated responses received.
COMPLETED
NA
47 participants
3 months
2014-11-05
Participant Flow
English and Spanish-speaking adult patients (18-76 years old) with diabetes in possession of cell phones who receive primary care at Sam Sandos Westside Family Health Center (Westside), a federally qualified community health center in the Denver Health integrated healthcare system in Denver, CO.
Exclusion criteria included a life expectancy less than six months, age \< 18 or \> 76, and either lacking possession of or inability to use a cell phone or glucometer.
Participant milestones
| Measure |
Text Intervention
Group of study participants who received the text message intervention over a 3-month period. Participants received text messages 7, 2, and 1 day(s) prior to each of their scheduled appointments as recorded in the Denver Health scheduling system, and also received text messages prompts 3 times per week asking them to provide fasting blood sugar readings.
|
|---|---|
|
Overall Study
STARTED
|
47
|
|
Overall Study
COMPLETED
|
47
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Chronic Care Management/Patient Relationship Management Proof of Concept
Baseline characteristics by cohort
| Measure |
Text Intervention
n=47 Participants
Group of study participants who received the text message intervention over a 3-month period.
|
|---|---|
|
Age, Categorical
<=18 years
|
0 Participants
n=5 Participants
|
|
Age, Categorical
Between 18 and 65 years
|
44 Participants
n=5 Participants
|
|
Age, Categorical
>=65 years
|
3 Participants
n=5 Participants
|
|
Age, Continuous
|
50.29 years
STANDARD_DEVIATION 11.24 • n=5 Participants
|
|
Sex: Female, Male
Female
|
30 Participants
n=5 Participants
|
|
Sex: Female, Male
Male
|
17 Participants
n=5 Participants
|
|
Region of Enrollment
United States
|
47 participants
n=5 Participants
|
PRIMARY outcome
Timeframe: 3 monthsPopulation: Group of study participants who received the text message intervention over a 3-month period.
Patient engagement was assessed by patient text message response rates and average response times. Response rates were calculated as a percentage from the number of patient-initiated text messages sent in response to a system-generated request for information (the numerator) divided by the total number of system-generated requests for information (the denominator). Average response times were calculated from system-recorded time stamps for outbound requests sent and inbound patient-initiated responses received.
Outcome measures
| Measure |
Text Intervention
n=47 Participants
Group of study participants who received the text message intervention over a 3-month period.
|
|---|---|
|
Patient Engagement
|
68.14 text message response rate (percent)
|
SECONDARY outcome
Timeframe: 3 monthsAs measured by no-show rates for appointments at all clinics during the study period, compared between intervention and control groups
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 3 monthsAs measured by comparison of patient responses to validated assessment instrument administered at baseline and post-intervention
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: 3 monthsMeasured by patients' self-reported fasting blood glucose levels during the intervention period and compared to previous laboratory data in the medical record.
Outcome measures
Outcome data not reported
Adverse Events
Text Intervention
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Andrew W. Steele, MD, MPH, MSc
Denver Health and Hospital Authority
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place