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One-Year Follow-Up Study on the Prognosis of Adult Patients with Generalized Anxiety Disorder

One-Year Follow-Up Prognosis Study in Adults with Generalized Anxiety Disorder - GAD-1YFU Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000059428
Enrollment
24
Registered
2025-10-23
Start date
2025-07-28
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

Generalized Anxiety Disorder

Interventions

None listed

Sponsors

Chiba University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria will be included: The primary diagnosis meets the diagnostic criteria for generalized anxiety disorder (DSM-5). Age between 18 and 65 years at the time of obtaining informed consent. Written informed consent is obtained voluntarily from the patient after receiving a sufficient explanation of the study and demonstrating adequate understanding. Usual treatment (regular consultations with a primary physician are mandatory, and the presence or absence of pharmacotherapy for generalized anxiety disorder at the time of entry is not restricted) is being provided, and no new initiation or additional changes in pharmacotherapy for generalized anxiety disorder are planned during the study period. Pharmacotherapy for generalized anxiety disorder refers to psychotropic medications such as antidepressants, anxiolytics, or hypnotics, regardless of indication. The patient is able to understand cognitive behavioral therapy and is in a mental and physical condition that allows for continuous practice for at least 16 weeks.

Exclusion criteria

Exclusion criteria: The following individuals will be excluded: Those with comorbid schizophrenia spectrum and other psychotic disorders, bipolar and related disorders, substance-related and addictive disorders, neurocognitive disorders, or neurodevelopmental disorders. Those at imminent risk of suicide. Those with serious physical illnesses such as cancer, heart disease, or stroke. Those with intellectual disability (estimated IQ < 80 based on the JART-25: Japanese Adult Reading Test-25 or similar measures). Those who have received cognitive behavioral therapy within the past six months. Any other individuals deemed unsuitable for safe participation in this study by the principal investigator or study therapists.

Design outcomes

Primary

MeasureTime frame
Assessment of anxiety using the Hamilton Anxiety Rating Scale (HAM-A)

Countries

Japan

Contacts

Public ContactItsuko Yoshida

Chiba University Cognitive Behavioral Physiology

tokiko.yoshida@chiba-u.jp0432262027

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026