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

Sponsor
University of California, Davis (Other)
Overall Status
Completed
CT.gov ID
NCT03538860
Collaborator
Agency for Healthcare Research and Quality (AHRQ) (U.S. Fed)
114
1
2
44.5
2.6

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Active comparator: Human interpreter
  • Behavioral: Intervention: Asynchronous Telepsychiatry
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
114 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
A Clinical Trial to Validate an Automated Online Language Interpreting Tool With Hispanic Patients Who Have Limited English Proficiency - Phase Two.
Actual Study Start Date :
Nov 14, 2017
Actual Primary Completion Date :
Jul 31, 2021
Actual Study Completion Date :
Jul 31, 2021

Arms and Interventions

Arm Intervention/Treatment
Other: Method A first then Method B

Conventional in-person interview with a psychiatrist with a live human interpreter with crossover to asynchronous telepsychiatry

Behavioral: Active comparator: Human interpreter
A Spanish-speaking patient is diagnostically assessed in-person by an English-speaking psychiatrist through a Spanish-speaking interpreter.

Behavioral: Intervention: 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.

Other: Method B first then Method A

Asynchronous telepsychiatry - that is, video-recorded interviews that are subsequently processed with automated speech recognition and machine translation technologies, with crossover to conventional in-person interview with a psychiatrist with a live human interpreter

Behavioral: Active comparator: Human interpreter
A Spanish-speaking patient is diagnostically assessed in-person by an English-speaking psychiatrist through a Spanish-speaking interpreter.

Behavioral: Intervention: 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.

Outcome Measures

Primary Outcome Measures

  1. Diagnostic accuracy [Measured at one time point by each psychiatrist, once both methods of interviews are completed in one day]

    Diagnosis accuracy with respect to gold standard SCID for Method B will be evaluated against Method A.

  2. Diagnostic Inter-rater reliability [Measured at one time point by each psychiatrist, once both methods of interviews are completed in one day]

    Using 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 Outcome Measures

  1. Satisfaction ratings [Measured at one time point by each psychiatrist, once both methods of interviews are completed in one day]

    Satisfaction ratings from patients' questionnaires

  2. Interview and language interpretation quality [Measured at one time point by each psychiatrist, once both methods of interviews are completed in one day]

    All 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

  3. Interview and language interpretation accuracy [Measured at one time point by each psychiatrist, once both methods of interviews are completed in one day]

    All 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

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 UC Davis Medical Center Sacramento California United States 95817

Sponsors and Collaborators

  • University of California, Davis
  • Agency for Healthcare Research and Quality (AHRQ)

Investigators

None specified.

Study Documents (Full-Text)

More Information

Publications

None provided.
Responsible Party:
University of California, Davis
ClinicalTrials.gov Identifier:
NCT03538860
Other Study ID Numbers:
  • 1131922
  • R01HS024949
First Posted:
May 29, 2018
Last Update Posted:
Oct 14, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University of California, Davis
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 14, 2021