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Clinical Trials/NCT04990492
NCT04990492UnknownNot Applicable

Interactive Voice Based Administration of the GAD 7

Oklahoma State University Center for Health Sciences2 sites in 1 country40 target enrollmentStarted: June 10, 2021Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
40
Locations
2
Primary Endpoint
GAD 7 Diagnostic Scores

Study Overview

Brief Summary

This study investigates a new delivery method for the General Anxiety Disorder - 7 (GAD 7), a clinically accepted tool for diagnosing general anxiety disorder. The new tool records auditory responses to the assessment and the study will examine if the instrument is effective at capturing participant depression levels. If proven effective, future studies may investigate if the new format can be used to improve at home clinical care.

Detailed Description

This study is an investigation of the construct validity and user experience of a new delivery system for the General Anxiety Disorder - 7 (GAD 7), a clinically accepted tool for diagnosing general anxiety disorder. The purpose of the study is to examine if the new delivery system of the GAD 7 is effective at capturing participant anxiety levels and to assess the differences of usability between the paper and voice administered versions. The voice administered version uses a Mirror device, which is similar to a smart television with a mirror interface. The device records auditory responses to the GAD 7 through Amazon Alexa. The investigators will be comparing the responses on the new device to those given on the clinically established paper format. If proven effective at capturing depression levels of patients, future studies may investigate if the new format can be used to improve at home clinical care.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Newly admitted patients to the Oklahoma State University Behavioral Medicine Clinic

Exclusion Criteria

  • Vulnerable populations, such as children (i.e., minors or individuals under the legal age of consent) and individuals who are incarcerated (i.e., prisoners), will be excluded.
  • Individuals who are not their own guardian (i.e., those suffering from severe disabilities) will also be excluded.

Outcomes

Primary Outcomes

GAD 7 Diagnostic Scores

Time Frame: Five minutes

Scores from the self administered assessment for general anxiety disorder

User Experience Questionnaire

Time Frame: Five minutes

Likert based questionnaire on user experience

Secondary Outcomes

  • Patient's Qualitative Responses(One minute)

Investigators

Sponsor
Oklahoma State University Center for Health Sciences
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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