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ZeroOCD: Learn to overcome contamination OCD with your smartphone: an Augmented Reality cognitive behavioral therapy app for obsessive-compulsive disorder

ZeroOCD: Learn to overcome contamination OCD with your smartphone: an Augmented Reality cognitive behavioral therapy app for obsessive-compulsive disorder: Randomized controlled trial and a feasibility study - ZeroOCD

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57913
Enrollment
83
Registered
2025-02-04
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-10

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

Conditions

obsessive-compulsive disorder, fear of contamination

Interventions

ZeroOCD provides (semi-)automated Augmented Reality (AR) Cognitive Behaviour Treatment (CBT) in 9 modules, which involve topics such as psychoeducation, case examples, exposure through AR, cognitive t

Sponsors

Vrije Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: OCD symptoms (scoring above 7 on the Y-BOCS diagnostic interview, self-report for the feasibility study)Fear of contamination OCD symptoms (scoring above 6 on the Padua Inventory - Contamination Fear Subscale) 18-64 years oldHave an access to a compatible smartphoneHave an internet connectionProficiency in one of the countries’ language (i.e., Dutch, Swedish, or German)Willing to participate in the research study and provide informed consent

Exclusion criteria

Exclusion criteria: Having been diagnosed with a bipolar or psychotic disorder (self-report)Fear of contamination being a symptom of other disorder than OCD, such as anxiety (based on a clinical judgment, Y-BOCS, GAD-7, SHAI)Severe depressive symptoms (PHQ-9 > 20 points at baseline)Reporting suicidality (PHQ-9, item 9 > 2 points at baseline)Parallel psychological treatmentNon-stable dosage of psychoactive medication during last 3 months or planned changes during the study period

Design outcomes

Primary

MeasureTime frame
The main study parameters are the post-intervention and the follow-up differences in OCD symptoms between the experimental and control condition, post-intervention and follow-up differences for the experimental condition compared to baseline, and the differences in costs between the three conditions. In the feasibility study, a number of parameters related to user-friendliness and usage of the app will be assessed.

Secondary

MeasureTime frame
In the RCT, secondary outcomes will include weekly index of OCD symptoms, anxiety symptoms, depressive symptoms, overall social functioning, quality of life, and substance use. In the feasibility study, secondary outcomes will involve treatment satisfaction, user experience, realism of the AR exposure, safety, usage, reasons for discontinuation, understanding of the treatment, technical alliance between patients and the platform, engagement, and OCD symptoms.

Countries

Netherlands, Sweden, Switzerland

Contacts

Public ContactT Donker

Vrije Universiteit

t.donker@vu.nl0205988959

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)