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临床试验/NCT03548545
NCT03548545Unknown不适用

Trancranial Direct Current Stiimulation as add-on Treatment to Cognitive-Behavior Therapy in People With Major Depression

University of Minho1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2018年3月28日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
72
试验地点
1
主要终点
Mood improvement

研究概览

简要总结

This is a parallel randomized, double-blinded, sham-controlled clinical trial in which a total of 72 drug-naïve MDD subjects (36 per arm) are randomized to one of two groups: Cognitive-Behavior Therapy (CBT) combined with either active or sham tDCS.

The primary outcome is mood improvement, as measured by the Montgomery-Asberg Depression Rating Scale (MADRS). The secondary outcome is to test whether tDCS combined with CBT can engage the proposed mechanistic target, of restoring the prefrontal imbalance and connectivity, by changes over EEG.

详细描述

Major Depression Disorder (MDD) is widely recognized as a staggering global healthcare challenge, as well as a potentially lethal illness. In Portugal, 7% of the population is diagnosed with depression every year, and suicide is responsible for more than a thousand deaths annually.

The current standard care for MDD involves the use of psychotherapy, antidepressant medication, or a combination of both. However, approximately 30% of people suffering from MDD exhibit depressive symptoms despite the appropriate psychological and pharmacological treatments. One option is to combine several treatments, usually by the use of drug augmentations and/or combinations of different drugs, which often increases the risk of adverse effects. Thus, it is important to study non-pharmacological interventions targeting mechanisms not directly involved with the regulation of neurotransmitters.

Cognitive-behavioral Therapy (CBT) is a well-established, and empirically-supported non-pharmacological treatment for depression, including for those that have not responded to antidepressants. However, several patients remain refractory to CBT.

tDCS is a safe, non-invasive, rather inexpensive, easy to administrate, and well-tolerated neuromodulatory technique. Several studies, including studies from our group, already shown that tDCS can be effective in MDD. However, tDCS seems to have a better effect when used as an add-on treatment to other intervention.

What is not known so far are the effects of using tDCS as add-on intervention to CBT on MDD symptoms.

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
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

Both the Participant, the outcome assessor and the Psychologist providing the CBT will be blinded to the type of the stimulation that the subject is receiving. Unblinding will occur at the end of the participation in the study and subjects that received sham tDCS will have the chance to receive the active tDCS.

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged 18-75 years;
  • •Unipolar, nonpsychotic MDD;
  • •Score in the MADRS between 7 and 34(mild to moderate depression);
  • •Low risk of suicide;
  • •Able to sign informed consent

排除标准

  • •Any contraindication to receive tDCS(such as metal in the head, implanted brain medical devices);
  • •any significant or unstable neurologic or psychiatric disorder other than MDD;2) history of substance abuse within the past 6-months;
  • •Any personality disorders; and
  • •any severe life-threatening Axis III disorders or concurrent medical condition likely to worsen patient's functional status in next 6-months such as; cancer, terminal heart, kidney, or liver disease.

研究组 & 干预措施

CBT combined with active tDCS

Experimental

Subjects allocated to this arm will receive cognitive-behavior therapy combined with active tDCS over the dorsolateral prefrontal cortex.

干预措施: tDCS (Device)

CBT combined with sham tDCS

Sham Comparator

Subjects allocated to this arm will receive cognitive-behavior therapy combined with sham tDCS over the dorsolateral prefrontal cortex.

干预措施: tDCS (Device)

结局指标

主要结局

Mood improvement

时间窗: Improvement defined as 50% decrease in the MADRS score at 4-week intervention. Cut-off points include: 0 to 6 - symptom absent, 7 to 19 - mild depression, 30 to 34 - moderate, 35 to 60 - severe depression.

Mood as assessed by the Montgomery-Asberg Depression Rating Scale(MADRS)

次要结局

  • EEG activity(Reduction of the inter-hemispheric imbalance over DLPFC at 4-week post-intervention sessions)

研究者

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

Sandra Carvalho

PhD

University of Minho

研究点 (1)

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