Efficacy and feasibility of software for the treatment of obsessive compulsive disorder: a pilot study

Efficacy and feasibility of software for the treatment of obsessive compulsive disorder: a pilot study - Efficacy and feasibility of software for the treatment of obsessive compulsive disorder: a pilot study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000048120

Enrollment

Registered

2022-06-21

Start date

2022-07-07

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

Obsessive compulsive disorder

Interventions

the software for the treatment of obsessive compulsive disorder for up to 8 wks

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients with obsessive compulsive disorder diagnosed by DSM-5.

Exclusion criteria

Exclusion criteria: High risk of suicide, self-harm, admission. Those who cannnot answer the questionnaire du to the lack of ability. Those who don't have computer or smartphone. Those who have received CBT or those who will receive CBT during this trial.

Design outcomes

Primary

Measure	Time frame
Yale-Brown Obsessive Compulsive Scale(Y-BOCS) at 8 wks, dropouts for any reason at 8wks	—

Secondary

Measure	Time frame
Patient Health Questionnaire(PHQ-9), Overall Anxiety Severity and Impairment Scale (OASIS), Obsessive-Compulsive Inventory-Revised (OCI-R), Alliance with Software: AS, free description about the software and the treatment at 8wks	—

Countries

Japan

Contacts

Public ContactHissei Imai

Kyoto University Health Promotion and Human Behavior, Graduate School of Medicine / School of Public Health

ihits@hotmail.com+81-75-753-9491

Outcome results

None listed

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