McLean Hospital
Belmont, Massachusetts, 02478, United States
Location status: Recruiting
NCT Number: NCT05630963
This study looks at the role of the Nociceptin/Orphanin FQ receptor system in the brain of individuals with current or past major depressive disorder (MDD). It also examines how individuals with a history of depression make certain decisions and which brain regions are involved in such decisions. Information collected through MRI, PET, biospecimens (i.e., blood, saliva) and behavioral tasks will be used to predict depressive symptoms in the future.
Interested in participating?
Request Info18 year–45 year
All sexes
Observational
Belmont, Massachusetts, 02478, United States
Location status: Recruiting
The overarching goals of this research are to investigate: (1) the activity of the Nociceptin/Orphanin FQ receptor system among individuals with current or remitted MDD; (2) neural foundations of approach/avoidance behaviors in current or remitted MDDs; (3) stress-induced inflammation in individuals with remitted MDD; (4) neural markers that predict future disease course.
This will be achieved through an innovative method of using functional magnetic resonance imaging (fMRI) during an approach/avoidance decision-making task, in addition to a resting positron emission tomography (PET) scan.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
for all participants:
Inclusion criteria
for "Remitted MDD" group:
Inclusion criteria
for "Current MDD" group:
Exclusion criteria
for all participants:
Electrotactile stimulation will be used as the aversive stimulus. The aversive stimulus is delivered in the form of a mild half-second stimulation to the ankle, calibrated to a subjective threshold that is uncomfortable but not painful. This stimulation is delivered by Digitimer DS8R Constant Current Stimulator (Digitimer North America, LLC. Ft. Lauderdale, FL). Its previous model DS71 has been safely implemented in studies with previously MGH-approved IRB's (Milad et al., 2013).
A Nociceptin/Orphanin FQ ("N/OFQ") peptide tracer ([11C] NOP-1A) will be used as the PET radiotracer. Approximately 10 mCi of this tracer will be delivered intravenously as a slow bolus over 60 seconds with beginning of the PET imaging acquisition. Approximately 60 ml of blood will be drawn from an artery throughout the dynamic PET acquisition in order to measure the blood N/OFQ levels.
Time frame: Baseline
For assessing psychological state
Time frame: Baseline
the PRT assesses individuals' ability to learn from rewards
Time frame: within 30 days of Screening Visit
For testing the neural correlates of approach-avoidance decision making behaviors
Time frame: Baseline
For assessing stress level
Time frame: within 30 days of Screening Visit
For assessing the Nociceptin/Oprhanin FQ receptor system activity
Time frame: Baseline
for PET modeling and assessing Nociceptin/Orphanin FQ levels in bloodstream
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
To assess psychological state changes
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of depressive symptoms
Time frame: Baseline
self-report measure of childhood trauma
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report with subscales measuring physical functioning, physical role functioning, social functioning, etc.
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of stress levels
Time frame: Baseline
self-report measure of positive and negative affect
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of satisfaction and enjoyment across domains (e.g., work, leisure, social relations)
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of pleasure
Time frame: Baseline
self-report measure of perception of being stuck in difficult situations
Time frame: Baseline
self-report measure of perception of defeat
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of unpredictability of parental environment growing up
Time frame: Baseline
self-report measure of mood symptom severity including 4 subscales related to depression and anxiety
Time frame: Baseline
Measures and differentiates between anxiety
Time frame: Baseline
self-report measure of participants' thoughts regarding the PRT task stimuli
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
self-report measure of ability to want and enjoy rewards
Time frame: Baseline
clinical measure of suicidality
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
clinical measure of depression severity
Time frame: Change from Baseline at 6 months and 12 months after the PET visit
clinical measure of depression severity
Time frame: Baseline
self-report measure of trait avoidance
Time frame: Change from Baseline at 12 months after the PET visit
self-report measure of lifetime exposure to acute and chronic stress that may affect mental and physical health
Contact information is provided by the study sponsor or research team.
David Crowley, ALM
CONTACT
Tracy Lam, BS
CONTACT
Mclean Hospital
Other
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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