Observational study on the use of ePRO (electronic patient reported outcomes) to assess depressive symptoms

Observational study on the use of ePRO (electronic patient reported outcomes) to assess depressive symptoms - Observational study on the use of ePRO to assess depressive symptoms

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000057034

Enrollment

300

Registered

2025-02-14

Start date

2023-07-13

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Depression, anxiety

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Persons aged 18 years or older 2) Patients with symptoms of depression or anxiety (due to the nature of the research, which involves the construction of a database for the voluntary registration of patients' subjective symptoms, the diagnosis will not be strictly limited to a narrow sense of the term, but will be broadly defined as depression or anxiety) 3) Persons who, after receiving sufficient written and verbal explanations regarding participation in this research, provide written consent through their own free will, with sufficient understanding 4) Those who can use information terminals such as smartphones and tablet PCs independently and who can continuously register data on the web by themselves for at least one year.

Exclusion criteria

Exclusion criteria: A person who the principal investigator or a sub-investigator deems unsuitable for conducting this study safely

Design outcomes

Primary

Measure	Time frame
Patient Health Questionnaire-9 (PHQ-9) Generalized Anxiety Disorder -7 (GAD-7)	—

Countries

Japan

Contacts

Public Contactyoichi seki

Chiba University Research Center for Child Development

yoichi-seki@chiba-u.jp043-226-2975

Outcome results