Gamified Cognitive Therapy for Obsessive Compulsive Disorder
Gamified Combined Cognitive Bias Modification in Adults Diagnosed With OCD: Randomized Controlled Trial
Recruiting
N/AInterventional Study
Obsessive Compulsive Disorder (OCD)
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Review the details below, then apply to join this clinical trial.
At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
90 (estimated)
Sponsor
Dokuz Eylul University · Other
Who this trial is looking for
This trial is looking for adults with obsessive-compulsive disorder (OCD) to test a mobile game aimed at improving OCD symptoms. Participants will use a mobile app with different therapy styles for four weeks and have follow-up assessments after that.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I have been diagnosed with obsessive-compulsive disorder (OCD)
I have stable psychiatric medication for at least one month
I have access to the internet and a mobile phone
I do not have any current suicidal thoughts or psychotic symptoms
I can perceive colored visual stimuli
I am not enrolled in another clinical trial
I am not receiving any other psychological treatment currently
You may not be able to join if
I have active suicidal thoughts or psychotic symptoms
My psychiatric medication has changed in the past month
I have a significant neurological or medical illness
I have visual impairments like color blindness
I am currently in another clinical trial for psychological treatment
I am receiving psychotherapy or psychological treatments outside this study
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
This randomized controlled trial examines the effects of a mobile-based gamified combined cognitive bias modification (CBM-C) intervention on obsessive-compulsive symptoms, obsessive beliefs, attentional and interpretation biases, depressive symptoms, and psychological distress. The gamified CBM-C condition is compared to a standard mobile-based CBM-C and a placebo control condition. All intervent…
This randomized controlled trial examines the effects of a mobile-based gamified combined cognitive bias modification (CBM-C) intervention on obsessive-compulsive symptoms, obsessive beliefs, attentional and interpretation biases, depressive symptoms, and psychological distress. The gamified CBM-C condition is compared to a standard mobile-based CBM-C and a placebo control condition. All interventions are delivered via a mobile application. Assessments are conducted at baseline, post-intervention (week 4), and 3-month follow-up.
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Eligibility Criteria
Inclusion Criteria:
* Age 18 years or older
* Primary diagnosis of obsessive-compulsive disorder (OCD), confirmed by a licensed clinician using the Structured Clinical Interview for DSM-5 (SCID-5)
* No current suicidal ideation or psychotic symptoms
* Access to the internet and a mobile phone
* Sta…
Inclusion Criteria:
* Age 18 years or older
* Primary diagnosis of obsessive-compulsive disorder (OCD), confirmed by a licensed clinician using the Structured Clinical Interview for DSM-5 (SCID-5)
* No current suicidal ideation or psychotic symptoms
* Access to the internet and a mobile phone
* Stable psychiatric medication use for at least one month prior to enrollment, with no changes in dosage during the 4-week intervention period
* No current neurological or medical condition that would interfere with participation
* Ability to perceive colored visual stimuli (e.g., no color blindness)
* Not currently enrolled in another intervention-based study
* Not receiving any other form of psychological treatment at the time of participation
Exclusion Criteria:
* Presence of active suicidal ideation or psychotic symptoms
* Unstable psychiatric medication use (e.g., recent dose change within the past month or expected change during the intervention period)
* Significant neurological or medical illness that may interfere with participation
* Visual impairments that would prevent accurate perception of colored stimuli (e.g., color blindness)
* Current participation in another clinical trial involving psychological intervention
* Receiving concurrent psychotherapy or other psychological treatments outside of the study
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