Obsessive-Compulsive Disorder Clinical Trial
— AvoidOCDOfficial title:
The Neurocircuitry of Relief During Avoidance Learning in Patients With Obsessive-compulsive Disorder
NCT number | NCT04685018 |
Other study ID # | bram vervliet |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 10, 2020 |
Est. completion date | May 1, 2022 |
To investigate the neuro-mechanisms underpinning persistent avoidance in OCD patients
Status | Recruiting |
Enrollment | 40 |
Est. completion date | May 1, 2022 |
Est. primary completion date | January 10, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Healthy volunteers 18-60 years old; - Participants are motivated and give written informed consent; - Adequate demand of Dutch language; - Subjects have never participated in a fear conditioning task; - Diagnosis of OCD (for OCD group only); - Contraindications for the MRI exam. Exclusion Criteria: - Current neurological (e.g. Epilepsia), respiratory, cardiovascular, metabolic, gastrointestinal, endocrine (especially diabetes), renal or urinary diseases, psychiatric disorder or other relevant medical histories (except for OCD in the OCD group); - Being pregnant or lactating; - Alcohol intake greater than 14 alcoholic units per week (one alcoholic unit = 10 gr ethanol); - History of cannabis use or any other drug of abuse during the 3 months prior to the study; - The medical doctor has asked to the participant to stay away from stressful situations; - Electronic implants (e.g., pacemaker); - Pain or other condition of the hand or the wrist. |
Country | Name | City | State |
---|---|---|---|
Belgium | Psychiatry | UZ Leuven campus Gasthuisberg | Leuven |
Lead Sponsor | Collaborator |
---|---|
KU Leuven |
Belgium,
Gillan CM, Morein-Zamir S, Urcelay GP, Sule A, Voon V, Apergis-Schoute AM, Fineberg NA, Sahakian BJ, Robbins TW. Enhanced avoidance habits in obsessive-compulsive disorder. Biol Psychiatry. 2014 Apr 15;75(8):631-8. doi: 10.1016/j.biopsych.2013.02.002. Epu — View Citation
Leknes S, Lee M, Berna C, Andersson J, Tracey I. Relief as a reward: hedonic and neural responses to safety from pain. PLoS One. 2011 Apr 7;6(4):e17870. doi: 10.1371/journal.pone.0017870. — View Citation
Milad MR, Furtak SC, Greenberg JL, Keshaviah A, Im JJ, Falkenstein MJ, Jenike M, Rauch SL, Wilhelm S. Deficits in conditioned fear extinction in obsessive-compulsive disorder and neurobiological changes in the fear circuit. JAMA Psychiatry. 2013 Jun;70(6) — View Citation
Vervliet B, Lange I, Milad MR. Temporal dynamics of relief in avoidance conditioning and fear extinction: Experimental validation and clinical relevance. Behav Res Ther. 2017 Sep;96:66-78. doi: 10.1016/j.brat.2017.04.011. Epub 2017 Apr 23. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Avoidance responses during the avoidance-relief task | Avoidance responses during avoidance learning and test will be recorded in terms of button press and Reaction times | 1 hour for avoidance task | |
Primary | Relief during the omissions of the US | Relief will be measured as:
Brain data during fMRI: whole-brain activations, as well as activations in specific regions of interest (ROI: VTA, NAcc, OFC) at the moment of the omissions of the electrical stimulation (US) during both the avoidance learning and the extinction learning phase of the avoidance-relief task; Individual ratings: relief pleasantness ratings measured on a Likert scale from 0 (neutral) to 3 (very pleasant) after each omission of the electrical stimulation (US) during both the avoidance learning and the extinction learning phase of the avoidance-relief task; Physiological data: skin conductance responses (SCR) at the moment of the omissions of the electrical stimulation (US) during both the avoidance learning and the extinction learning phase of the avoidance-relief task. |
1 hour to perform the avoidance task | |
Secondary | Tolerance to stress | The individual level of tolerance to distress will be measured via the self-administration of the Distress Tolerance Scale | 1 hour to perform the avoidance task | |
Secondary | Therapeutic outcome in OCD | The therapeutic outcome in OCD individuals will be evaluated by using the Y-BOCS (self-administered) questionnaire | 1 hour to perform the avoidance task | |
Secondary | Resting-state connectivity | The strength of connectivity between NAcc, VTA, and OFC, will be measured during the resting state MRI acquisition | 1 hour to perform the avoidance task |
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