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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

47 participants

Primary outcome timeframe

3 months

Results posted on

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

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

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 months

Population: 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

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 months

As 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 months

As 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 months

Measured 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 events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

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

Phone: 303-602-9773

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place