Identification of Depressive and Anxiety Symptoms Among a Sample of Emergency Department Patients Using Artificial Intelligence (AI) Technology

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Hospitals Cleveland Medical Center

About this trial

Behavioral health problems, such as depression and anxiety, are common yet often are not identified by emergency department doctors and nurses. These mental health conditions can be due to medical issues or can worsen medical problems. One way investigators hope to do a better job of learning about mental health is by training Artificial Intelligence (AI) software to detect anxiety and depression by analyzing facial expression and tone of voice.

Participants are invited to participate in a study which may help improve emergency department care. An audio and video recording of the participant's responses to some simple, non-psychological questions will be analyzed by a computer to determine whether investigators can assess mood and anxiety by analyzing speech and visual patterns. The audio and video will not be listened to nor watched by study personnel, only analyzed by a computer. The investigator's hope is that it will help others in the future by aiding in the assessment of psychological state. This study is being conducted at CMC ED only.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients (age 18 and over) who presents to the UHCMC ED voluntarily with no obvious psychological disturbance by self-report or nurse/provider initial assessment

English-speaking

Patients with non-emergent concerns of Emergency Severity Index (ESI) level 3, 4, or 5

Disqualifiers

Prisoners

Patients who are deemed to be critically ill (including life or limb threatening illness) or unable to consent

Non-English Speaking

Trial design

Design model

Single group

Treatments tested in this trial

  • Biometrics (or AI Biomaker)

    Device

    Patients will be asked to read a story and their facial expressions and audio cues will be recorded.

Treatment groups

30 Participants
are divided into 1 treatment group
Group A: Participants seen at University Hospitals Cleveland Medical Center Emergency DepartmentExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Percentage of participants who score 5-9 on the PHQ-9

Patient Health Questionnaire (PHQ-9) is a multipurpose instrument for screening, diagnosing, monitoring, and measuring severity of depression. Questions are scored on a Likert scale of 0-3 with 0 being not at all and 3 being nearly every day.

Time frame
Baseline
2

Percentage of participants who score 10-14 on the PHQ-9

Patient Health Questionnaire (PHQ-9) is a multipurpose instrument for screening, diagnosing, monitoring, and measuring severity of depression. Questions are scored on a Likert scale of 0-3 with 0 being not at all and 3 being nearly every day.

Time frame
Baseline
3

Percentage of participants who score 15-19 on the PHQ-9

Patient Health Questionnaire (PHQ-9) is a multipurpose instrument for screening, diagnosing, monitoring, and measuring severity of depression. Questions are scored on a Likert scale of 0-3 with 0 being not at all and 3 being nearly every day.

Time frame
Baseline
4

Percentage of participants who score 20-27 on the PHQ-9

Patient Health Questionnaire (PHQ-9) is a multipurpose instrument for screening, diagnosing, monitoring, and measuring severity of depression. Questions are scored on a Likert scale of 0-3 with 0 being not at all and 3 being nearly every day.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: