Survey of daily life difficulties in patients with tardive dyskinesia

Survey of factors affecting QOL in patients with tardive dyskinesia - Survey of factors affecting QOL in patients with tardive dyskinesia

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000045565

Enrollment

100

Registered

2021-09-27

Start date

2021-10-05

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

Tardive dyskinesia

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: -Patients who provide their informed consent to participate in this study -Patients who are 20 or older and diagnosed with tardive dyskinesia (DSM-5 code: 333.85) based on DSM-5 criteria -Patients who have self-awareness of their involuntary movements

Exclusion criteria

Exclusion criteria: -Patients who are judged inappropriate as the subject by researchers -Patients who withdraw their consent to participate in this study

Design outcomes

Primary

Measure	Time frame
-VAS Score -Annoyances (Activities that make you feel distress)	—

Secondary

Measure	Time frame
-Average score for each question	—

Countries

Japan

Contacts

Public ContactYumi Watanabe

Mitsubishi Tanabe Pharma Corporation Medical Intelligence department

watanabe.yumi@mf.mt-pharma.co.jp06-6205-5417

Outcome results