Oxytocin and Cognitive Control in Adult ADHD
- Conditions
- Attention Deficit/Hyperactivity Disorder
- Interventions
- Drug: Placebo nasal spray
- Registration Number
- NCT03136263
- Lead Sponsor
- Massachusetts General Hospital
- Brief Summary
This is a randomized, double-blind, placebo-controlled crossover study of single-dose intranasal oxytocin (24 IU) in 18-55 year-old men with attention deficit/hyperactivity disorder (ADHD). Following a screening visit to determine eligibility, participants will return for two main study visits. During the main study visits, study participants will receive either oxytocin (Syntocinon® nasal spray, Victoria Pharmacy, Zürich, Switzerland) or placebo (inactive ingredients of Syntocinon® nasal spray, Victoria Pharmacy), followed by assessments of cognitive control over attention and behavior. Twenty-four participants will be randomized 1:1 to one of two drug orders, i.e., oxytocin - placebo or placebo - oxytocin. In an additional neuroimaging substudy, a subset of participants will undergo task-based and resting-state functional magnetic resonance imaging (fMRI) following oxytocin/placebo administration to investigate the effects of oxytocin on fMRI activation and functional connectivity within the cognitive control network.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Male
- Target Recruitment
- 24
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Drug order: Oxytocin - placebo Placebo nasal spray - Drug order: Placebo - oxytocin Oxytocin nasal spray - Drug order: Placebo - oxytocin Placebo nasal spray - Drug order: Oxytocin - placebo Oxytocin nasal spray -
- Primary Outcome Measures
Name Time Method Stop-signal task First and second main study visits (1-4 weeks apart) Mean difference in performance on the stop-signal task between the oxytocin and placebo visits (e.g., stop-signal reaction time)
- Secondary Outcome Measures
Name Time Method AX-CPT First and second main study visits (1-4 weeks apart) Mean difference in performance on the AX-CPT between the oxytocin and placebo visits (AY and BX responses)
Category switch task First and second main study visits (1-4 weeks apart) Mean difference in performance on the category switch task between the oxytocin and placebo visits (switch costs and target congruency effect)
Global/local task First and second main study visits (1-4 weeks apart) Mean difference in performance on the global/local task between the oxytocin and placebo visits (global precedence effect)
Simon task First and second main study visits (1-4 weeks apart) Mean difference in performance on the Simon task between the oxytocin and placebo visits (Simon effect and Garner effect)
Trial Locations
- Locations (1)
Massachusetts General Hospital
🇺🇸Boston, Massachusetts, United States