Single Session Personalized Aperiodic Transcranial Alternating Current Stimulation (PandA-tACS) for Antenatal Depression (PandA)
Single Session Personalized Aperiodic Transcranial Alternating Current Stimulation (PandA-tACS) for Antenatal Depression: A Randomized, Sham-Controlled Trial (R61 Phase)
研究概览
详细说明
The purpose of this study is to evaluate the safety, feasibility, tolerability, and brain effects of a single session of a personalized form of non-invasive brain stimulation called PandA-tACS in individuals with antenatal depression. PandA-tACS uses each participant's own EEG activity to create an individualized stimulation waveform. Participants will be females aged 18-45 years who are 14-32 weeks pregnant with a viable, low-risk singleton pregnancy and meet criteria for unipolar, non-psychotic major depressive disorder. Participants must be at low suicide risk, and be able to complete study procedures.
Participants will complete screening, informed consent, clinical assessments, pregnancy safety review, and high-density EEG recordings. Eligible participants will attend one in-person stimulation visit and will be randomized to receive PandA-tACS, individualized alpha-frequency tACS, or sham stimulation. Stimulation will be delivered through scalp electrodes while participants are monitored by trained study staff. EEG, symptom ratings, blood pressure, pre-natal safety checks, and adverse event monitoring will be completed before and/or after stimulation. Optional MRI may be completed for electric-field modeling. Pregnancy and birth outcomes will be reviewed through the medical record.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Flavio Frohlich, PhD
- 电话号码:919-966-9929
- 邮箱:flavio_frohlich@med.unc.edu
研究联系人备份
- 姓名:Athena Stein, PhD
- 电话号码:919-966-9929
- 邮箱:Athena_Stein@med.unc.edu
参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion Criteria:
- Aged 18 - 45
- Capacity to understand all relevant risks and potential benefits of the study as determined by study staff (provision of informed consent) Stated willingness to comply with all study procedures and availability for the duration of the study
- Low suicide risk (defined for this study as no active suicidal ideation in the past month and no suicide attempts, preparatory actions, or significant non-suicidal self-harm in the previous 2 years). Risk will be assessed utilizing the C-SSRS screen and triage version with further exploration of positive responses.
- Between weeks 14-32 of viable singleton pregnancy
- Currently meet DSM-5 criteria of unipolar, non-psychotic MDD which is confirmed by the DIAMOND
- HDRS-17 score ≥8
Exclusion Criteria:
- DSM-5 diagnosis of severe alcohol use disorder (AUD) within the last 12 months, as evidenced by the DIAMOND
- DSM-5 diagnosis of moderate to severe substance use disorder (excluding tobacco) within the last 12 months, as evidenced by the DIAMOND
- Lifetime history of bipolar disorder, as evidenced by DIAMOND
- Schizophrenia spectrum and other psychotic disorders, as evidenced by DIAMOND
- History of autism spectrum disorder
- Initiated any new psychotropic medication in the 6 weeks prior to screening or had a dose change or discontinuation in the preceding 6 weeks
- Initiated a new course of psychotherapy in the 6 weeks preceding screening
- Received any neurostimulation treatment in the 6 weeks preceding screening
- History of seizures (excluding febrile seizures in childhood or Electroconvulsive Therapy (ECT) induced seizures)
- Neurological disorders that would increase risk of participation or present a significant confounder in the opinion of the investigator (for example, dementia, history of stroke, Parkinson's disease, multiple sclerosis, history of traumatic brain injury with prolonged loss of consciousness, ruptured cerebral aneurysm, previous CNS radiation)
- Previously failed to respond to ECT or transcranial magnetic stimulation (TMS)
- Prior brain surgery and/or brain implants
- Implanted medical device that uses electricity
- Currently enrolled in another clinical trial for depression
History of any of the following conditions:
- Diabetes (gestational or general history)
- Pre-term delivery (<37 weeks)
- Eclampsia
- Pre-eclampsia with severe features
- Asthma requiring daily medication
- Chronic hypertension
- Immune thrombocytopenia (ITP)
- Hyperthyroidism requiring medication
- Pre-pregnancy BMI 40 or more
- In vitro fertilization (IVF)
- Mullerian anomaly of uterus
- Organ transplant
- Prior history of deep vein thrombosis/pulmonary embolism (DVT/PE) or plan for anticoagulation during pregnancy
- Fetus with autoimmune hydrops
- Abnormal placenta
Current pregnancy:
- HIV/Hep B/Hep C with detectable viral loads
- Anemia [Hemoglobin under 11.0] upon entry to pre-natal care
- No scheduled pre-natal visits by 15 weeks
- Placenta previa
- Placenta accreta spectrum (PAS)
- Pre-eclampsia
- Gestational diabetes
- Gestational hypertension
- Fetus with abnormal chromosomes
- Cervical length < 2.5 cm
- Presence of cerclage or vaginal progesterone to decrease chance of pre-term labor
- Fetal growth restriction
- Macrosomia
- Polyhydramnios
- Oligohydramnios
- Rupture of membranes
- Hyperemesis Gravidarum (HEG)
- Confirmation testing for Tri 13/18/21
- Congenital anomalies on anatomy ultrasound that do not resolve with follow-up ultrasound
学习计划
研究是如何设计的?
设计细节
- 主要用途:基础科学
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:三倍
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
假比较器:Inactive Sham (placebo)
Participants will receive sham tACS.
Sham stimulation mimics all procedures used in active stimulation.
|
Participants will be fitted with the same electrode setup and receive sham (placebo) tACS delivered using the neuroConn DC Stimulator MC.
|
|
有源比较器:Active IAF-tACS: Experimental Arm
Participants will receive active IAF-tACS delivered at the participant's individual alpha frequency, as measured by EEG.
2mA will be delivered at Cz, and 1 mA (antiphase) split between F3/F4 (in phase).
IAF-tACS is delivered in 4 x blocks of 10 min, separated by 2 min HD-EEG.
|
Participants will be fitted with the same electrode setup and receive IAF-tACS delivered using the neuroConn DC Stimulator MC.
|
|
实验性的:Active PandA-tACS: Experimental Arm
Participants will receive active PandA-tACS delivered with the participant's flatter aperiodic slope, as measured by EEG.
2mA will be delivered at Cz, and 1 mA (antiphase) split between F3/F4 (in phase).
PandA-tACS is delivered in 4 x blocks of 10 min, separated by 2 min HD-EEG.
|
Participants will be fitted with the same electrode setup and receive PandA-tACS delivered using the neuroConn DC Stimulator MC.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Safety via the presence of any serious AEs
大体时间:Day 1 to within 90 days of expected delivery date.
|
The number of serious adverse events (SAEs) deemed at least potentially related to PandA-tACS.
|
Day 1 to within 90 days of expected delivery date.
|
|
Tolerability of PandA-tACS
大体时间:Immediately after intervention
|
Proportion of participants reporting stimulation intolerance or unable to complete stimulation due to tolerability.
|
Immediately after intervention
|
|
Feasibility of PandA-tACS
大体时间:Through completion of the study, roughly 2 years
|
Total number of enrolled participants.
Must be at least 45 overall, and 15 per group.
|
Through completion of the study, roughly 2 years
|
|
Change in aperiodic slope in the dlPFC region.
大体时间:Immediately before and after 40 minutes of stimulation (on single interventional session day).
|
Pre- to post-stimulation change in left dorsolateral prefrontal cortex (dlPFC) aperiodic slope (beta coefficient/exponent) derived from resting high-density (HD-EEG).
The endpoint will be compared for PandA-tACS versus IAF-tACS and sham.
|
Immediately before and after 40 minutes of stimulation (on single interventional session day).
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Correlation between modeled left dorsolateral prefrontal cortex (dlPFC) electric field strength and pre- to post-stimulation change in left dlPFC aperiodic slope
大体时间:Immediately before and after 40 minutes of stimulation (on single interventional session day).
|
Within the PandA-tACS group, correlation between modeled left dlPFC electric field strength and pre- to post-stimulation change in left dlPFC aperiodic slope.
|
Immediately before and after 40 minutes of stimulation (on single interventional session day).
|
合作者和调查者
调查人员
- 首席研究员:Flavio Frohlich, PhD、University of North Carolina, Chapel Hill
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 26-1564
- R61MH144538 (美国 NIH 拨款/合同)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
IPD 共享时间框架
IPD 共享访问标准
IPD 共享支持信息类型
- 研究方案
- 树液
- 分析代码
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.