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Validation of an Automated Online Language Interpreting Tool - Phase Two.

A Clinical Trial to Validate an Automated Online Language Interpreting Tool With Hispanic Patients Who Have Limited English Proficiency - Phase Two.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03538860
Enrollment
114
Registered
2018-05-29
Start date
2017-11-14
Completion date
2021-07-31
Last updated
2021-10-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anxiety Disorder, Chronic Medical Condition, Mood Disorder, Substance Use Disorder

Keywords

Telepsychiatry, AsynchronousTelepsychiatry, Automated Translation

Brief summary

There is a pressing national need to provide higher-quality, more effectively accessible language interpretation services to improve the health outcomes of Americans who have limited English proficiency (LEP). This project addresses a critical component of this problem: The need to improve access to high quality, mental health services for diverse populations by improving the flow of clinical work across care settings (primary care and specialty care) through the use of innovative online asynchronous methods of language interpretation and clinical communication. The investigators are conducting a two phase study. The first phase is completed and involved developing and testing the interpreting tool. The second phase of the research is a clinical trial to compare two methods of cross-language psychiatric assessment.

Detailed description

The investigators propose to develop and test a novel automated asynchronous interpretation tool. The proposed project builds on previous research, piloting the automated asynchronous interpretation tool. This 5-year project will be conducted in two phases. In Phase 1 the investigators iteratively evaluate and refine the automated asynchronous interpretation tool already developed in prior studies. In Phase 2, the investigators evaluate this tool using a two-group randomized cross-over trial. Investigators compare: * Method A (current gold standard of in-person real-time interpreting practice). A Spanish-speaking patient is diagnostically assessed in-person by an English-speaking psychiatrist through a Spanish-speaking interpreter. * Method B (comparative practice - ATP). A Spanish-speaking patient is interviewed in Spanish by a trained mental health interviewer. The interview is recorded in real time, translated into English using the automatic interpretation tool and adding sub-titles to the video file, and sent to an English-speaking psychiatrist to asynchronously - that is, at a later time - review the video and make a diagnosis. All patients will undergo evaluation by both methods. Half of the patients will be randomized to be assessed by Method A first, followed by Method B and half to be assessed by Method B first, followed by Method A. The specific aims of the study are : * Aim 1: To iteratively evaluate and refine the automated asynchronous interpretation tool already developed in prior studies. * Aim 2: To compare patient satisfaction of Method A vs. Method B. * Aim 3: To compare the diagnostic accuracy and psychiatrist inter-rater reliability of Method A vs. Method B and demonstrate psychiatrist inter-rater reliability for Method B. * Aim 4: To compare the interview and language interpretation quality and accuracy of Method A vs. Method B.

Interventions

BEHAVIORALActive comparator: Human interpreter

A Spanish-speaking patient is diagnostically assessed in-person by an English-speaking psychiatrist through a Spanish-speaking interpreter.

BEHAVIORALIntervention: Asynchronous Telepsychiatry

A Spanish-speaking patient is interviewed in Spanish by a trained mental health interviewer. The interview is video-recorded in real-time, automatically translated into English with sub-titles added to the video file, and sent to a psychiatrist and to 3 English-speaking psychiatrists to asynchronously review the video and make a diagnosis.

Sponsors

Agency for Healthcare Research and Quality (AHRQ)
CollaboratorFED
University of California, Davis
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Inclusion Criteria: Hispanic patients with significant Limited English proficiency (LEP) * aged 18 or older * diagnosis of a mood disorder, anxiety disorder, or substance/alcohol abuse disorder(s) * Diagnosis of a chronic medical condition * referred by PCP or self-referral with PCP informed

Exclusion criteria

Criteria: * less than 18 years * imminent suicidal ideation and/or plans * immediate violent intentions or plans * significant cognitive deficits * patient who's PCP recommends not participating.

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic accuracyMeasured at one time point by each psychiatrist, once both methods of interviews are completed in one dayDiagnosis accuracy with respect to gold standard SCID for Method B will be evaluated against Method A.
Diagnostic Inter-rater reliabilityMeasured at one time point by each psychiatrist, once both methods of interviews are completed in one dayUsing independent assessments from four psychiatrists for each of the 100 method B interviews the investigators will also examine inter-rater reliability of Method B diagnosis.

Secondary

MeasureTime frameDescription
Satisfaction ratingsMeasured at one time point by each psychiatrist, once both methods of interviews are completed in one daySatisfaction ratings from patients' questionnaires
Interview and language interpretation qualityMeasured at one time point by each psychiatrist, once both methods of interviews are completed in one dayAll 200 interviews in both methods will be video recorded and the audio transcribed. The investigators will measure and compare the two interview methods interpretation quality through perception of interpretation quality
Interview and language interpretation accuracyMeasured at one time point by each psychiatrist, once both methods of interviews are completed in one dayAll 200 interviews in both methods will be video recorded and the audio transcribed. The investigators will measure and compare the two interview methods accuracy through the presence of medical errors, and the presence of language errors

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026