Trial Outcomes & Findings for Effectiveness and Implementation of eScreening in Post 9/11 Transition Programs (NCT NCT04506164)
NCT ID: NCT04506164
Last Updated: 2026-02-17
Results Overview
Proportion of newly enrolled Veterans who received PTSD screening (i.e., The Primary Care PTSD Screen for DSM-5 \[PC-PTSD-5\]) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the rate of screening (i.e., the proportion of Veterans who received the screening measure versus those who did not) during each phase, and then compared the proportion of Veterans who received screening during the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
COMPLETED
NA
72 participants
within 30 days of enrollment at the VA study site during each phase
2026-02-17
Participant Flow
Aim 2: Survey data was collected from 72 staff members who were enrolled in the study. This aim did not involve study groups/arms. Note: For Aim 1 deidentified patient level eScreening data from 15484 veterans was collected from the electronic medical record. Veterans did not directly participate, thus no Veterans were recruited/enrolled.
Unit of analysis: VHA Medical Center
Participant milestones
| Measure |
Cohort 1
Screening As Usual/Pre-Implementation (Months 1-3), Active eScreening Implementation (Months 4-12), Implementation Sustainment (Months 13-21).
|
Cohort 2
Screening As Usual/Pre-Implementation (Months 4-6), Active eScreening Implementation (Months 7-15), Implementation Sustainment (Months 16-24).
|
Cohort 3
Cohort 3: Screening As Usual/Pre-Implementation (Months 7-9), Active eScreening Implementation (Months 10-18), Implementation Sustainment (Months 19-27).
|
Cohort 4
Cohort 4: Screening As Usual/Pre-Implementation (Months 10-12), Active eScreening Implementation (Months 13-21), Implementation Sustainment (Months 22-30).
|
|---|---|---|---|---|
|
Pre Implementation
STARTED
|
653 2
|
1261 2
|
984 2
|
1025 2
|
|
Pre Implementation
Staff Participants
|
5 2
|
9 2
|
9 2
|
6 2
|
|
Pre Implementation
COMPLETED
|
653 2
|
1261 2
|
984 2
|
1025 2
|
|
Pre Implementation
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
|
Implementation
STARTED
|
1327 2
|
2686 2
|
1808 2
|
1431 2
|
|
Implementation
Staff Participants
|
6 2
|
9 2
|
4 2
|
3 2
|
|
Implementation
COMPLETED
|
1327 2
|
2686 2
|
1808 2
|
1431 2
|
|
Implementation
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
|
Sustainment
STARTED
|
824 2
|
1332 2
|
1022 2
|
1131 2
|
|
Sustainment
Staff Participants
|
4 2
|
8 2
|
8 2
|
1 2
|
|
Sustainment
COMPLETED
|
824 2
|
1332 2
|
1022 2
|
1131 2
|
|
Sustainment
NOT COMPLETED
|
0 0
|
0 0
|
0 0
|
0 0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
Baseline characteristic data, including age, was not collected from the 72 staff participants.
Baseline characteristics by cohort
| Measure |
Pre Implementation
n=3923 Participants
Pre-implementation/Screening As Usual phase
|
Implementation
n=7252 Participants
eScreening implementation phase
|
Sustainment
n=4309 Participants
Sustainment phase
|
Staff
n=72 Participants
Staff participants
|
Total
n=15556 Participants
Total of all reporting groups
|
|---|---|---|---|---|---|
|
Age, Customized
Mean Veteran age
|
34.24 years
STANDARD_DEVIATION 11.23 • n=3923 Participants • Baseline characteristic data, including age, was not collected from the 72 staff participants.
|
34.10 years
STANDARD_DEVIATION 10.93 • n=7252 Participants • Baseline characteristic data, including age, was not collected from the 72 staff participants.
|
36.48 years
STANDARD_DEVIATION 11.60 • n=4309 Participants • Baseline characteristic data, including age, was not collected from the 72 staff participants.
|
—
|
34.94 years
STANDARD_DEVIATION 11.25 • n=15484 Participants • Baseline characteristic data, including age, was not collected from the 72 staff participants.
|
|
Sex: Female, Male
Female
|
804 Participants
n=3923 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
1465 Participants
n=7252 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
806 Participants
n=4309 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
0 Participants
Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
3075 Participants
n=15484 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
|
Sex: Female, Male
Male
|
3119 Participants
n=3923 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
5787 Participants
n=7252 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
3503 Participants
n=4309 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
0 Participants
Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
12409 Participants
n=15484 Participants • Baseline characteristic data, including sex, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
American Indian or Alaska Native
|
71 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
172 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
95 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
338 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
Asian
|
182 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
376 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
228 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
786 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
|
0 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
0 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
0 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
0 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
Black or African American
|
642 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
1177 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
602 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
2421 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
White
|
2353 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
4351 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
2585 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
9289 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
More than one race
|
0 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
0 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
0 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
0 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Race (NIH/OMB)
Unknown or Not Reported
|
675 Participants
n=3923 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
1176 Participants
n=7252 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
799 Participants
n=4309 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
—
|
2650 Participants
n=15484 Participants • Baseline characteristic data, including race, was not collected from the 72 staff participants
|
|
Region of Enrollment
United States
|
3923 Participants
n=3923 Participants
|
7252 Participants
n=7252 Participants
|
4309 Participants
n=4309 Participants
|
72 Participants
n=72 Participants
|
15556 Participants
n=15556 Participants
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phaseProportion of newly enrolled Veterans who received PTSD screening (i.e., The Primary Care PTSD Screen for DSM-5 \[PC-PTSD-5\]) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the rate of screening (i.e., the proportion of Veterans who received the screening measure versus those who did not) during each phase, and then compared the proportion of Veterans who received screening during the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Compare Rate of PTSD Screening During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
724 Participants
|
1408 Participants
|
893 Participants
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phaseProportion of newly enrolled Veterans who received depression screening (Patient Health Questionnaire-2; PHQ-2) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the rate of screening (i.e., the proportion of Veterans who received the screening measure versus those who did not) during each phase, and then compared the proportion of Veterans who received screening during the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Compare Rate of Depression (PHQ-2) Screening During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
744 Participants
|
1433 Participants
|
905 Participants
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phaseProportion of newly enrolled Veterans who received alcohol screening (AUDIT) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the rate of screening (i.e., the proportion of Veterans who received the screening measure versus those who did not) during each phase, and then compared the proportion of Veterans who received screening during the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Compare Rate of Alcohol Screening (AUDIT) During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
761 Participants
|
1494 Participants
|
929 Participants
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phase.Proportion of newly enrolled Veterans who received suicide screening (Columbia-Suicide Severity Rating Scale; CSSRS) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the rate of screening (i.e., the proportion of Veterans who received the screening measure versus those who did not) during each phase, and then compared the proportion of Veterans who received screening during the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Compare Rate of Suicide Screening (CSSRS) During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
831 Participants
|
1588 Participants
|
989 Participants
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phase.Number of days to receive PTSD screening (PC-PTSD-5) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the time to screening (in days) during each phase, and then compared the time to screening for the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Time to PTSD Screening (PC-PTSD-5) Completion During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
27.90 Number of days
Standard Deviation 7.47
|
27.94 Number of days
Standard Deviation 7.26
|
27.74 Number of days
Standard Deviation 7.42
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phase.Number of days to depression screening (PHQ-2) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the time to screening (in days) during each phase, and then compared the time to screening for the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Time to Depression (PHQ-2) Screening Completion During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
27.83 Number of days
Standard Deviation 7.53
|
27.88 Number of days
Standard Deviation 7.33
|
27.70 Number of days
Standard Deviation 7.46
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phase.Number of days to alcohol screening (AUDIT) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the time to screening (in days) during each phase, and then compared the time to screening for the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Time to Alcohol Screening (AUDIT) Completion During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
27.78 Number of days
Standard Deviation 7.59
|
27.74 Number of days
Standard Deviation 7.49
|
27.56 Number of days
Standard Deviation 7.63
|
PRIMARY outcome
Timeframe: within 30 days of enrollment at the VA study site during each phase.Number of days to suicide screening (CSSRS) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase. For this outcome, we calculated the time to screening (in days) during each phase, and then compared the time to screening for the eScreening implementation and sustainment phases vs. screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=3923 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=7252 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=4309 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Time to Suicide Screening (CSSRS) Completion During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
27.30 Number of days
Standard Deviation 8.22
|
27.30 Number of days
Standard Deviation 8.27
|
27.02 Number of days
Standard Deviation 8.49
|
PRIMARY outcome
Timeframe: 30 days from the date the screener was administered during each phase.Change in rate of referral to mental health follow up care (BHIP) following a positive PTSD screen (PC-PTSD-5) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=233 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=433 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=341 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Change in Rate of Referral to Mental Health Care Following Positive PTSD Screen (PC-PTSD-5) During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation.
|
31 Participants
|
32 Participants
|
34 Participants
|
PRIMARY outcome
Timeframe: 30 days from the date the screener was administered during each phase.change in rate of referral to mental health follow up care (BHIP) following a positive depression (PHQ-2) screen during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=168 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=323 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=224 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Change in Rate of Referral to Mental Health Care Following Positive Depression Screen (PHQ-2) During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
31 Participants
|
28 Participants
|
27 Participants
|
PRIMARY outcome
Timeframe: 30 days from the date the screener was administered during each phasechange in rate of referral to substance use treatment following a positive alcohol screen (AUDIT) during the eScreening implementation and sustainment phases compared to the screening as usual/pre-implementation phase.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=214 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=408 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=278 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
Change in Rate of Referral to Substance Use Treatment Following Positive Alcohol Screen (AUDIT) During eScreening Implementation and Sustainment vs. Screening as Usual/Pre-implementation
|
5 Participants
|
10 Participants
|
7 Participants
|
SECONDARY outcome
Timeframe: Surveys were administered within 60 days of initiating each phase: pre-implementation, implementation, and sustainmentStaff survey responses on the Patient Perspectives domain of the PRISM Contextual Survey Instrument (PCSI). The PCSI includes 29 items rated on a 5-point Likert scale, where 1 = strongly disagree and 5= strongly agree; thus higher scores represent more positive perspectives.
Outcome measures
| Measure |
Screening As Usual/Pre-implementation
n=29 Participants
Usual screening procedures were used (i.e., verbal/interview or self-report, paper-based screening measures).
|
eScreening Implementation
n=21 Participants
electronic screening (eScreening) was implemented using the MCIS.
|
Sustainment
n=22 Participants
This phase immediately followed the eScreening implementation phase and did not involve any active implementation.
|
|---|---|---|---|
|
PRISM Contextual Survey Instrument (PCSI)
|
3.8 score on a scale
Standard Deviation .52
|
4.2 score on a scale
Standard Deviation 3.5
|
3.9 score on a scale
Standard Deviation .74
|
Adverse Events
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place