- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05944172
Impact of Attention on Obsessive Thoughts Through THOUGHT (THOUGHTS)
Thoughts Content in OCD: What Links Between Mind Wandering and Obsessions
Study Overview
Status
Conditions
Detailed Description
We developed a scale (the THOUGHTS) dedicated to allow a subject to subjectively measure its level of mind wandering/daydreaming (and obsessions in case of OCD patients) during different everyday situations. This scale is developed for 15 years old or older students (high school, university). Indeed, common point in everyday life was easier to find in students than in workers where lifestyle can be very divergent according to the job type. Through this scale, we will first detect the situations the more associated with mind wandering/daydreaming in healthy subjects. To do that, we will first find the 50% and the 25% of the situations the most associated with mind wandering. This step will allow us to distinguish two types of situations: situations with high level of mind wandering/daydreaming vs. situations with low level of mind wandering/daydreaming. Then we will do the same analyses in OCD patients to see if situations of high level of mind wandering are the same in both groups. Finally, we will compare the level of obsessions in OCD patients in these two types of situations (linked with high vs. low mind wandering, as defined by healthy subject, OCD patients and both populations).
To make these analyses, we will recruit 40 young OCD people (still students) from only one center, all diagnosed through DSM-5 criteria by a same senior and experimented child and adolescent psychiatrist and 40 matched healthy subjects.
For OCD patients: all comorbidities will be allowed except those associated with hallucinations or delusions: schizophrenia or bipolar disorder will then not be allowed. Neurological disorders will not be allowed too. Y-BOCS or CY-BOCS will be get and analyzed to find if severity could influence our results.
Healthy controls: they will be recruited to be matched with the OCD patients. No psychiatric or neurologic disorder will be allowed. No psychotropic or neurologic treatment will be allowed.
Finally, in terms of statistics, we will use non parametric tests.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Creteil
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Créteil, Creteil, France, 94010
- Albert Chenevier hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
For pathological patients:
- Over the age of 15
- Suffering from OCD (obsessive compulsive disorder)
- All comorbidities are possible except schizophrenia, bipolarity and anorexia nervosa
- Consultant or admitted to Albert Chenevier Hospital
For patients who are not affected by the disease:
- Over 15 years of age
- Consulted or admitted to GH Henri Mondor
Exclusion Criteria:
For pathological patients:
- Refusal to participate by the patient (and/or legal representative in the case of minors)
- Presence of schizophrenia, bipolar or anorexia nervosa
For patients who are free of these conditions:
- Presence of psychiatric or neurological pathology
- Refusal to participate on the part of the patient (and/or on the part of the legal representative in the case of minors)
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Comparison of the obsession level (as measured by the THOUGHTS-scale) in situations associated with high level mind wandering/daydreaming and situations associated with low level of mind wandering/daydreaming
Time Frame: metrics are measured only one time, directly after the subject accept to participate to the study.
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demonstrate that in patients with OCD, the level of presence of obsessions is different during active and passive situations, using the THOUGHT questionnaire - scale.
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metrics are measured only one time, directly after the subject accept to participate to the study.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
: Effect of OCD severity on the link between OCD and mind wandering/daydreaming
Time Frame: measured only one time, directly after the subject accept to participate to the study.
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Separated OCD patients in 2 groups according to their YBOCS severity to see if obsessions replace mind wandering in the same manner (the same situation and at the same level)
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measured only one time, directly after the subject accept to participate to the study.
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- APHP220613
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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