Remote Training in Evidence-based Practices for Clinicians Who Work With Migrant Workers
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ClinicalTrials.gov Identifier: NCT03515226 |
Recruitment Status :
Terminated
(Challenges in recruiting eligible participants)
First Posted : May 3, 2018
Results First Posted : December 1, 2021
Last Update Posted : December 1, 2021
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Depression | Behavioral: ITS based training Behavioral: Traditional Training | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 25 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | Randomized clinical trial |
Masking: | None (Open Label) |
Primary Purpose: | Health Services Research |
Official Title: | Remote Training in Evidence-based Practices for Clinicians Who Work With Migrant Workers |
Actual Study Start Date : | June 30, 2018 |
Actual Primary Completion Date : | June 30, 2020 |
Actual Study Completion Date : | August 30, 2020 |

Arm | Intervention/treatment |
---|---|
Active Comparator: Traditional Training
20 hours of didactic education and training in CBT principles, depression assessment and cultural competency and 25 hours in dyad role playing of CBT manualized treatment sessions with supervision.
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Behavioral: Traditional Training
Training using didactics and role plays |
Experimental: ITS based training
Traditional training plus the addition of an algorithmic based training computer program that trains clinicians in clinical micro-competencies.
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Behavioral: ITS based training
Training using computerized adaptive training in addition to role play |
- Acceptability of Intervention Measure (AIM) - Goal Setting [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention acceptability; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total scale range is 4-20. Each group will be compared on the degree they find the specific clinical skill acceptable to use after they complete the training. We administered the AIM twice asking the students to respond to the acceptability of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on goal setting.
- Acceptability of Intervention Measure (AIM) - Identifying Challenges [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention acceptability; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total scale range is 4-20. Each group will be compared on the degree they find the specific clinical skill acceptable to use after they complete the training. We administered the AIM twice asking the students to respond to the acceptability of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on identifying challenges.
- Intervention Appropriateness Measure (IAM) - Goal Setting [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention appropriateness; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total range for this measure is 4-20. Each group will be compared on the degree they find the specific clinical skill appropriate to use after they complete the training. We administered the IAM twice asking the students to respond to the acceptability of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on goal setting.
- Intervention Appropriateness Measure (IAM) - Identifying Challenges [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention appropriateness; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total scale range is 4-20. Each group will be compared on the degree they find the specific clinical skill appropriate to use after they complete the training. We administered the IAM twice asking the students to respond to the acceptability of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on identifying challenges.
- Feasibility of Intervention Measure (FIM) - Goal Setting [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention feasibility; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total scale range is 4-20. Each group will be compared on the degree they find the specific clinical skill feasible to use after they complete the training they participated in. We administered the FIM twice asking the students to respond to the feasibility of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on goal setting.
- Feasibility of Intervention Measure - Identifying Challenges [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]This is a four item measure of intervention feasibility; where each item is rated on a 1-5 scale, with 1 = not at all appropriate and 5 = very appropriate. The total scale range is 4-20. Each group will be compared on the degree they find the specific clinical skill feasible to use after they complete the training they participated in. We administered the FIM twice asking the students to respond to the feasibility of goal setting as a clinical skill and of identifying challenges as a clinical skill. This section reports on identifying challenges.
- Intervention Usability Scale (IUS) - Goal Setting [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]The IUS is a 10-item measure with a possible total score ranging from 0 to 100; higher scores indicate a more usable intervention. Although this measure has not yet been normed as a measure of intervention usability, the System Usability Scale upon which the IUS is based defines scores of 70 or above as indicative of acceptable usability.
- Intervention Usability Scale (IUS) - Identifying Challenges [ Time Frame: This measure will be administered to participants in each training group after they complete the 25 hours of training. ]The IUS is a 10-item measure with a possible total score ranging from 0 to 100; higher scores indicate a more usable intervention. Although this measure has not yet been normed as a measure of intervention usability, the System Usability Scale upon which the IUS is based defines scores of 70 or above as indicative of acceptable usability.

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- BA level social work student
- Bilingual Spanish Speaking
Exclusion Criteria:
- none

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03515226
United States, Washington | |
University of Washington Department of Psychiatry and Behavioral Sciences | |
Seattle, Washington, United States, 98105 |
Principal Investigator: | Patricia Arean | UWMC Psychiatry | |
Study Director: | Brenna Renn, PhD | UWMC Psychiatry |
Documents provided by Eugene Aisenberg, University of Washington:
Responsible Party: | Eugene Aisenberg, Associate Professor, School of Social Work; Adjunct Associate Professor, Health Services, University of Washington |
ClinicalTrials.gov Identifier: | NCT03515226 |
Other Study ID Numbers: |
STUDY00004268 1P50MH115837-01 ( U.S. NIH Grant/Contract ) |
First Posted: | May 3, 2018 Key Record Dates |
Results First Posted: | December 1, 2021 |
Last Update Posted: | December 1, 2021 |
Last Verified: | November 2021 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Yes |
Plan Description: | We will be creating a register of study outcomes for all projects under the UW ALACRITY center that researchers and request permission to access. |
Supporting Materials: |
Study Protocol Statistical Analysis Plan (SAP) Informed Consent Form (ICF) Clinical Study Report (CSR) Analytic Code |
Time Frame: | Data for this study will be made available in January of 2021 |
Access Criteria: | Any interested party who wishes to use our data for research or educational purposes may contact Dr. Renn who will review the request and provide access to information requested. |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
workforce development intelligent tutoring systems |
Depression Behavioral Symptoms |