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Use of Artificial Intelligence based medical technology for screening anxiety and depression

Innovative medical technology for screening of anxiety and depression - N/A

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/07/054984
Enrollment
180
Registered
2023-07-10
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

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

Conditions

Health Condition 1: F411- Generalized anxiety disorder

Interventions

Sponsors

TerraBlue XT(P) Ltd.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Subject is willing and able to give informed consent for participation in the study. 2.Subjects with DSM 5 clinical diagnosis of unipolar depression mood and GAD 3.Severity of anxiety and depression confirmed by PHQ-9 and GAD-7. 4.Male or Female of age 18 â?? 60 years

Exclusion criteria

Exclusion criteria: 1.Subjects with other psychotic disorders 2.Any neurological disorders such as any significant head injury, epilepsy, Parkinsonâ??s disease, neuro-degenerative disorders etc. 3.Subjects of substance use disorders 4.Pregnant and lactating women

Design outcomes

Primary

MeasureTime frame
To validate the AI powered wearable device algorithm for detecting Generalized Anxiety Disorder (GAD) and Depressive Disorder (unipolar and recurrent depressive disorder) with a minimum acceptable sensitivity rate of 80% and specificity rate of 70 %.Timepoint: Screening or Baseline Visit

Secondary

MeasureTime frame
To validate whether technology can be used reliably for screening of common mental health disorders, like anxiety and depressionTimepoint: Screening or Baseline Visit

Countries

India

Contacts

Public ContactPriya Ranjan Pattanaik

TerraBlue XT

raji@teblux.com9886036987

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026