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Gamified Acceptance & Commitment Therapy for Benzodiazepine Discontinuation: Randomised controlled trial

Gamified Acceptance & Commitment Therapy for Benzodiazepine Discontinuation: Randomised controlled trial - Gamified ACT for Benzodiazepine Discontinuation: RCT

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000023580
Enrollment
40
Registered
2016-09-15
Start date
2017-04-01
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

Benzodiazepine Discontinuation

Interventions

Intervention: Gamified acceptance &amp
commitment therapy for benzodiazepine discontinuation Period: 5 weeks Intervention: Psychoeducation program Period: 5 weeks

Sponsors

Nagoya City University Graduate School of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Regular use: 5 times a week and over Required use: 4 times a week and less Use for infomnia: Before sleeping 2.Being prescrived benzodiazepine regulary 12 weeks and over. 3.Being prescribed benzodiazepine once a day and over.(Excluded only for required use or use for insomnia) 4.Willing to stop using benzodiazepine and treating physician determine eligibility to stop benzodiazepine. 5.Being able to access the program and having an Email address for daily use. 6. Having no plan to be hospitalized more than 1 week for any reason. 7.Having no plan to transfer to a different hospital within 4 months. 8.Being able to respond to assessments via telephone. 9.Being able to understand and sign a written informed consent.

Exclusion criteria

Exclusion criteria: 1.Being regulary prescribed 3 types of benzodiazepine and over. (excluded required use or use for insomnia) 2.Actively satisfied diagnostic cliteria with Mini-International Neuropsychiatric Interview. 3.Being regularly prescribed antipsychotic or mood stabilizer (lithium, valproate, carbamazepine and lamotrigine) 4.Imminent risk of suicide as judged by the treating physician. 5.Currently participating in another clinical intervention study. 6. Family members living with the researchers of the present study.

Design outcomes

Primary

MeasureTime frame
The success rate of benzodiazepine discontinuation during the 11th and 12th week after beginning of the program

Secondary

MeasureTime frame
Benzodiazepine reduction rate,Recovery Assessment Scale(RAS),Depression Anxiety Stress Scale(DASS),Severity of Dependence syndrome(SDS),Euro Qol 5 Dimension(EQ5-D),Cognitive Fusion Questionnaire(CFQ),Personal Values Questionnaire II (PVQ-II)

Countries

Japan

Contacts

Public ContactToshitaka ii

Nagoya City University Graduate School of Medical Sciences Department of Psychiatry,

tshtk.ii@gmail.com052-851-5511

Outcome results

None listed

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