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.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

72 participants

Primary outcome timeframe

within 30 days of enrollment at the VA study site during each phase

Results posted on

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

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

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 phase

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.

Outcome measures

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 phase

Proportion 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

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 phase

Proportion 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

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

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

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

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

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

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

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

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 phase

change 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

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 sustainment

Staff 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

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 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

James Pittman, PhD

VA San Diego Healthcare System

Phone: 858-552-8585

Results disclosure agreements

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