Trial Outcomes & Findings for Interactive Spaced Education to Optimize Hypertension Management (NCT NCT00904007)
NCT ID: NCT00904007
Last Updated: 2019-02-05
Results Overview
A unique hypertensive period served as the unit of analysis. A hypertensive period started on the first day during the study when a patient's BP was elevated. It ended on the first subsequent day when it was \<140/90 mm Hg or on the last day BP was recorded during the study. Duration of the hypertensive period (days) was the outcome measure. BP measurements obtained in the course of routine care were used to ascertain study outcomes, whether obtained by the PCP or at other clinic visits. These measurements were obtained from structured data (ie, BP recordings in the electronic medical record) and natural language processing of provider notes as previously described. If several measurements were recorded on the same day, the lowest mean arterial BP was used.
COMPLETED
NA
111 participants
Months 1-24
2019-02-05
Participant Flow
Participant milestones
| Measure |
SE Game Cohort
SE game clinicians were e-mailed one question every 3 days. Adaptive game mechanics re-sent questions in 12 or 24 days if answered incorrectly or correctly, respectively. Clinicians retired questions by answering each correctly twice consecutively. Posting of relative performance among peers fostered competition.
|
Control Cohort
Control clinicians received identical educational content in an online posting with email reminders.
|
|---|---|---|
|
Overall Study
STARTED
|
55
|
56
|
|
Overall Study
COMPLETED
|
55
|
56
|
|
Overall Study
NOT COMPLETED
|
0
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Interactive Spaced Education to Optimize Hypertension Management
Baseline characteristics by cohort
| Measure |
SE Game Cohort
n=55 Participants
SE game clinicians were e-mailed one question every 3 days. Adaptive game mechanics re-sent questions in 12 or 24 days if answered incorrectly or correctly, respectively. Clinicians retired questions by answering each correctly twice consecutively. Posting of relative performance among peers fostered competition.
|
Control Cohort
n=56 Participants
Control clinicians received identical educational content in an online posting with email reminders.
|
Total
n=111 Participants
Total of all reporting groups
|
|---|---|---|---|
|
Age, Continuous
|
50.5 years
STANDARD_DEVIATION 9.7 • n=99 Participants
|
53.1 years
STANDARD_DEVIATION 8.5 • n=107 Participants
|
51.8 years
STANDARD_DEVIATION 9.2 • n=206 Participants
|
|
Sex: Female, Male
Female
|
35 Participants
n=99 Participants
|
38 Participants
n=107 Participants
|
73 Participants
n=206 Participants
|
|
Sex: Female, Male
Male
|
20 Participants
n=99 Participants
|
18 Participants
n=107 Participants
|
38 Participants
n=206 Participants
|
PRIMARY outcome
Timeframe: Months 1-24A unique hypertensive period served as the unit of analysis. A hypertensive period started on the first day during the study when a patient's BP was elevated. It ended on the first subsequent day when it was \<140/90 mm Hg or on the last day BP was recorded during the study. Duration of the hypertensive period (days) was the outcome measure. BP measurements obtained in the course of routine care were used to ascertain study outcomes, whether obtained by the PCP or at other clinic visits. These measurements were obtained from structured data (ie, BP recordings in the electronic medical record) and natural language processing of provider notes as previously described. If several measurements were recorded on the same day, the lowest mean arterial BP was used.
Outcome measures
| Measure |
SE Game Cohort
n=55 Participants
SE game clinicians were e-mailed one question every 3 days. Adaptive game mechanics re-sent questions in 12 or 24 days if answered incorrectly or correctly, respectively. Clinicians retired questions by answering each correctly twice consecutively. Posting of relative performance among peers fostered competition.
|
Control Cohort
n=56 Participants
Control clinicians received identical educational content in an online posting with email reminders.
|
|---|---|---|
|
Cross-cohort Comparison of the Average Time Needed to Normalize Patients' Blood Pressure
|
137 days
Interval 0.0 to 365.0
|
145 days
Interval 0.0 to 365.0
|
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 13-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 13-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-24Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Month 1Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
SECONDARY outcome
Timeframe: Months 1-12Population: PI and project staff no longer have access to the raw data and are no longer able to generate any more data analyses.
Outcome measures
Outcome data not reported
Adverse Events
Arm 1
Arm 2
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Dr. B. Price Kerfoot
Veterans Affairs Boston Healthcare System
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place