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临床试验/NCT02737033
NCT02737033Unknown4 期

Effects of 800mg of Rhodiola Rosea in Attention in Adults With Attention-Deficit/Hyperactivity Disorder

Hospital de Clinicas de Porto Alegre1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年4月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
入组人数
60
试验地点
1
主要终点
Change in Stop Signal Task

研究概览

简要总结

This study evaluates the use of Rhodiola rosea in the attention of adults with Attention Deficit/Hyperactivity Disorder (ADHD). Half of participants will receive Rhodiola rosea 800mg, while the other half will receive 800mg of placebo.

详细描述

The evaluation of new therapies in adults with Attention Deficit/Hyperactivity Disorder (ADHD) may be clinically useful. Rhodiola rosea is an herbal medicine used for centuries in various medical conditions. Many randomized controlled trials have evaluated its usefulness in stress and fatigue. There were benefits in attention in some of these studies. Mild side effects and beneficial antioxidant properties make reasonable an assessment of its potential benefits in adults with ADHD. To our knowledge, Rhodiola rosea has never been studied in adults with ADHD.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Fulfillment of Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, (DSM-5) diagnostic criteria for ADHD in Adults
  • Intelligence Quotient (IQ) above 70
  • Eligibility to Rhodiola rosea

排除标准

  • clinical contraindication to Rhodiola rosea
  • any unstable chronic illness without proper treatment (hypertension, heart, kidney or liver disease, etc)
  • any significant neurological disease (delirium, dementia, epilepsy, AIDS, head trauma, multiple sclerosis, stroke, etc)
  • unstable psychiatric comorbidities requiring immediate treatment (risk of suicide, current Substance Use Disorder, etc.)
  • pregnant, nursing or absence of reliable contraception
  • current use of nicotine (<30 days)
  • use of anticoagulants
  • current use of any psychoactive drug (<30 days)
  • prior use of stimulants
  • current or lifetime psychosis
  • current or lifetime bipolar disorder

研究组 & 干预措施

Rhodiola

Experimental

Rhodiola rosea 800mg single dose

干预措施: Rhodiola (Drug)

Placebo

Placebo Comparator

placebo 800mg single dose

干预措施: Placebo (Drug)

结局指标

主要结局

Change in Stop Signal Task

时间窗: Baseline and 4 hours

Change from baseline attention 4 hours after a single dose of Rhodiola 800mg or placebo

次要结局

  • Change in Wechsler Adult Intelligence Scale (WAIS) - Digit Span subtest(Baseline and 4 hours)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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