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NCT Number: NCT05630963

Beyond Monoamines: The Role of the Nociceptin/Orphanin FQ Receptor in Major Depression

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.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Observational

Primary location

McLean Hospital

Belmont, Massachusetts, 02478, United States

Location status: Recruiting

Location contact

Tracy Lam, BS

CONTACT

[email protected]

617-855-4437

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for all participants:

  • All genders, races, and ethnic origins, aged between 18 and 45
  • Capable of providing written informed consent, and fluent in English
  • Right-handed
  • Absence of any psychotropic medications for at least 2 weeks
  • Has a smartphone (iPhone or Android) (needed for Ecological Momentary Assessment)

Inclusion criteria

for "Remitted MDD" group:

  • Meets inclusion criteria for all subjects, plus:
  • History of MDD as defined by DSM-5
  • Absence of anxiety disorder for the past two months

Inclusion criteria

for "Current MDD" group:

  • Meets inclusion criteria for all subjects, plus:
  • Presence of MDD as defined by DSM-5
  • Absence of anxiety disorder for the past two months

Exclusion criteria

for all participants:

  • Subjects with suicidal ideation where outpatient treatment is determined unsafe by the study clinician. These patients will be immediately referred to appropriate clinical treatment
  • Pregnant women or women of childbearing potential who are not using a medically accepted means of contraception (defined as oral contraceptive pill or implant, condom, diaphragm, spermicide, IUD, s/p tubal ligation, or partner with vasectomy)
  • Serious or unstable medical illness, including cardiovascular, hepatic, renal, respiratory, endocrine, neurologic or hematologic disease
  • History of seizure disorder
  • History of psychiatric illnesses, other than depression or anxiety disorders among the Current MDD and Remitted MDD groups
  • History of substance use disorder or alcohol use disorder (as these terms are defined by DSM-5); except depressed subjects may have a history of 'Mild' substance/alcohol use disorder only if it ended as least 12 months ago
  • History of cocaine or stimulant use or dopaminergic drugs
  • History or current diagnosis of dementia, or a score of < 26 on the Mini Mental State Examination at the screening visit;
  • Patients with mood congruent or mood incongruent psychotic features
  • Current use of other psychotropic drugs
  • Clinical or laboratory evidence of hypothyroidism
  • Patients with a lifetime history of electroconvulsive therapy (ECT)
  • Failure to meet standard MRI safety requirements
  • Abnormal ECG and lab results
  • History of seizure disorder
  • Contraindications for arterial line (e.g., abnormal result on Allen test, Raynaud's syndrome, history of anemia or bleeding disorder, history of fainting from blood draws).

Treatment and study plan

Aversive stimuli

Device

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).

PET radiotracer

Drug

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.

Primary outcomes

  1. Clinical Interview

    Time frame: Baseline

    For assessing psychological state

  2. Behavioral Performance on the Probabilistic Reward Task (PRT)

    Time frame: Baseline

    the PRT assesses individuals' ability to learn from rewards

  3. MRI Data

    Time frame: within 30 days of Screening Visit

    For testing the neural correlates of approach-avoidance decision making behaviors

  4. Salivary Cortisol

    Time frame: Baseline

    For assessing stress level

  5. PET Data

    Time frame: within 30 days of Screening Visit

    For assessing the Nociceptin/Oprhanin FQ receptor system activity

  6. Arterial blood data

    Time frame: Baseline

    for PET modeling and assessing Nociceptin/Orphanin FQ levels in bloodstream

  7. Follow-up Clinical Interviews

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    To assess psychological state changes

Secondary outcomes

  1. Beck Depression Inventory-II (BDI)

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    self-report measure of depressive symptoms

  2. Childhood Trauma Questionnaire (CTQ)

    Time frame: Baseline

    self-report measure of childhood trauma

  3. Medical Outcome Survey-Short form (SF-36)

    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.

  4. Perceived Stress Scale (PSS)

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    self-report measure of stress levels

  5. Positive and Negative Affect Schedule (PANAS)

    Time frame: Baseline

    self-report measure of positive and negative affect

  6. Quality of Life Enjoyment and Satisfaction Questionnaire (Q-LES-Q)

    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)

  7. Snaith Hamilton Pleasure Scale (SHAPS)

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    self-report measure of pleasure

  8. Thought and Feeling Questionnaire (TFQ)

    Time frame: Baseline

    self-report measure of perception of being stuck in difficult situations

  9. Defeat Scale (DS)

    Time frame: Baseline

    self-report measure of perception of defeat

  10. Questionnaire of Unpredictability in Childhood (QUIC)

    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

  11. Mood and Anxiety Symptom Questionnaire (MASQ)

    Time frame: Baseline

    self-report measure of mood symptom severity including 4 subscales related to depression and anxiety

  12. State-Trait Anxiety Inventory (STAI)

    Time frame: Baseline

    Measures and differentiates between anxiety

  13. PRT Post-task Questionnaire

    Time frame: Baseline

    self-report measure of participants' thoughts regarding the PRT task stimuli

  14. Temporal Experience of Pleasure Scale (TEPS)

    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

  15. Columbia-Suicide Severity Rating Scale (C-SSRS)

    Time frame: Baseline

    clinical measure of suicidality

  16. Hamilton-Depression Rating Scale (HAMD-17)

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    clinical measure of depression severity

  17. Quick Inventory of Depressive Symptomatology (QIDS)

    Time frame: Change from Baseline at 6 months and 12 months after the PET visit

    clinical measure of depression severity

  18. Cognitive-Behavioral Avoidance Scale (CBAS)

    Time frame: Baseline

    self-report measure of trait avoidance

  19. Stress and Adversity Inventory (STRAIN)

    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

Study contacts

Contact information is provided by the study sponsor or research team.

David Crowley, ALM

CONTACT

[email protected]

617-855-4432

Tracy Lam, BS

CONTACT

[email protected]

617-855-4437

Sponsors and collaborators

Lead sponsor

Mclean Hospital

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Nov 30, 2022
Registry last updated
Oct 21, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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