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临床试验/NCT07464886
NCT07464886招募中3 期

Prefrontal Glutamatergic Modulation by N-acetylcysteine and Mindfulness-based Cognitive Therapy for Mild Depression in Youth

University of Cincinnati1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2026年2月26日最近更新:
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
160
试验地点
1
主要终点
Glutamate levels in the left ventrolateral prefrontal cortex (VLPFC)

研究概览

简要总结

The primary goal is to investigate to what extent changes in glutamate and glutathione modulation and functional integration between brain networks associated with emotion and attention regulation are associated with treatment response in mildly depressed youth.

详细描述

The specific goals are to determine whether treatment with a combination of mindfulness-based cognitive therapy (MBCT) and N-acetylcysteine (NAC) enhances changes in left ventrolateral prefrontal cortex (VLPFC) and anterior cingulate cortex (ACC) glutamate and glutathione levels, and cortical-subcortical functional connectivity (Fc) compared with MBCT alone or NAC alone. The central hypothesis is that modulating glutamatergic output in the prefrontal cortex (PFC) and improving the cortical-subcortical functional connectivity (Fc) underlie treatment response in this population. The rationale for testing this hypothesis with a randomized controlled trial of NAC and MBCT, integrated with imaging, is that NAC is a glutamate modulator, MBCT has evidence for improving PFC-limbic Fc, both interventions have preliminary evidence for treating depression or mood symptoms have a benign safety profile. The investigators have a well-established record of conducting intervention studies integrating magnetic resonance spectroscopy (1H-MRS) and resting state functional magnetic resonance imaging (rs-fMRI) to study the neurophysiology of mood disorders. The university health center associated clinics provide the investigators access to the target population of this study. Therefore, the investigators are well positioned to investigate the neurobiological mechanisms associated with treatment response to glutamatergic modulation in mildly depressed youth. In this study, the specific aims are:

Aim 1: To determine to what extent glutamate levels in the left VLPFC change in response to treatment with NAC and/or MBCT in mildly depressed youth. The investigators will utilize 1H-MRS to measure changes in the left VLPFC glutamate following eight-week treatment with NAC and/or MBCT. The investigators predict that MBCT combined with NAC will lead to greater increases in left VLPFC glutamate levels compared with either MBCT or NAC alone.

Aim 2: To determine to what extent Fc within PFC-limbic circuits and within large-scale brain networks change in response to treatment with NAC and/or MBCT in mildly depressed youth. The investigators will utilize rs-fMRI to identify changes in Fc between the PFC (VLPFC, ACC) and subcortical regions, and within large scale brain networks associated with emotion and attention regulation (cingulo-opercular, fronto-parietal, and default mode networks). The investigators predict that MBCT combined with NAC will lead to greater increases in Fc compared with either MBCT or NAC alone.

Exploratory Aim 3: To investigate the role of central and peripheral biomarkers of oxidative stress and inflammation in predicting response to treatment to NAC and/or MBCT for mild depression in youth. The investigators will explore the role of central glutathione and peripheral thiobarbituric acid reactive substances (TBARS), malondialdehyde (MDA), high-sensitivity C-reactive protein (hs-CRP), interleukin-1β (IL-1β), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) in predicting response to treatment to NAC and/or MBCT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
15 Years 至 24 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • age between 15 years, 0 months to 24 years, 11 months old;
  • presenting with mild depression, defined by meeting DSM-5 criteria for a current major depressive episode, mild severity, or persistent depressive disorder, or other specified depressive disorder (depressive episode with insufficient symptoms to meet criteria for a major depressive episode);
  • medication-naïve or medication free for at least 5 half-lives since the last use of a psychoactive medication, with the exception of stimulants for ADHD;
  • if on ADHD stimulant medication over 2 months prior to screening, willing to maintain stimulant dose constant during the study participation;
  • Tanner stage greater than or equal to III;

排除标准

  • significant suicidal risk, defined by suicidal ideation of type 3, 4 or 5 on the Columbia Suicide Severity Rating Scale (C-SSRS) in the past 3 months, or any lifetime suicidal attempts;
  • current major depressive episode, moderate or severe
  • current or lifetime history of manic or hypomanic episodes, and/or diagnosis of bipolar disorder;
  • current or lifetime history of psychotic disorders, and/or prior diagnosis of schizophrenia spectrum disorders;
  • active or current substance use disorders in the last 3 months, except cannabis or alcohol use disorder, mild;
  • diagnosis of autism spectrum disorder, pervasive developmental disorder, obsessive-compulsive disorder, post-traumatic stress disorders, Tourette's syndrome
  • any contraindication to MRI scanning;
  • history of major neurological disorder (e.g, epilepsy), or head trauma with > 10 minutes loss of consciousness;
  • intellectual disability (IQ less than or equal to 70), as determined by the Weschler Abbreviated Scale of Intelligence (WASI);
  • previous participation in any mindfulness-based treatment;
  • initiating psychotherapy within 2 months prior to screening, or planning to initiate psychotherapy during study participation; if on therapy, frequency and type should remain stable for 2 months prior to enrollment and during study participation;
  • no current diagnosis of asthma
  • history of allergic reaction to N-acetylcysteine

研究组 & 干预措施

NAC plus MBCT

Active Comparator

N-acetylcysteine 2400 mg daily and mindfulness-based cognitive therapy over 8 weeks

干预措施: N-acetylcysteine (Drug)

NAC plus MBCT

Active Comparator

N-acetylcysteine 2400 mg daily and mindfulness-based cognitive therapy over 8 weeks

干预措施: Mindfulness-based cognitive therapy (Behavioral)

Placebo plus MBCT

Placebo Comparator

Placebo capsules and mindfulness-based cognitive therapy over 8 weeks

干预措施: Mindfulness-based cognitive therapy (Behavioral)

Placebo plus MBCT

Placebo Comparator

Placebo capsules and mindfulness-based cognitive therapy over 8 weeks

干预措施: Placebo (Drug)

NAC plus sham MBCT

Sham Comparator

N-acetylcysteine 2400 mg daily and sham mindfulness-based intervention over 8 weeks

干预措施: N-acetylcysteine (Drug)

NAC plus sham MBCT

Sham Comparator

N-acetylcysteine 2400 mg daily and sham mindfulness-based intervention over 8 weeks

干预措施: Sham mindfulness-based intervention (Behavioral)

Placebo plus sham MBCT

Other

Placebo capsules daily and sham mindfulness-based intervention over 8 weeks

干预措施: Placebo (Drug)

Placebo plus sham MBCT

Other

Placebo capsules daily and sham mindfulness-based intervention over 8 weeks

干预措施: Sham mindfulness-based intervention (Behavioral)

结局指标

主要结局

Glutamate levels in the left ventrolateral prefrontal cortex (VLPFC)

时间窗: From baseline to week 8

Changes in glutamate levels, measured by proton spectroscopy, in the left VLPFC following 8-week treatment with NAC and/or MBCT.

次要结局

  • Functional connectivity (Fc) within prefrontal cortex-limbic circuits and within large-scale brain networks(From baseline to week 8)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Fabiano Nery

Principal Investigator

University of Cincinnati

研究点 (1)

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