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临床试验/NCT06183372
NCT06183372已完成不适用

A Randomised Double-blind Placebo-controlled Acute Trial of Encapsulated Lemon Balm Efficacy and Tolerance on Calmness and Mood During Periods of Cognitive Demand

University of Reading2 个研究点 分布在 1 个国家目标入组 123 人开始时间: 2023年12月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
123
试验地点
2
主要终点
Calmness 9-point Likert Scale

研究概览

简要总结

This study aims to investigate the effect of a single dose (300mg) of encapsulated aqueous lemon balm extract on measures of calmness and mood during periods of cognitive demand over the course of the day in healthy adults aged 18-40 years with moderate stress (PSS entry between 14 to 26).

详细描述

Cognitive overload can be a common occurrence in an information saturated world (Eppler et al., 2008; Graf et al., 2021; Pass et al., 2004), and chronic cognitive overload is considered an initiating step in the emergence of various physical and emotional health concerns, likely due to high processing demands on the working memory neural system (Graf et al., 2021). Over time, psychological and physiological stress may arise, however current chemical interventions may be unsuitable for those experiencing mild-to-moderate levels of stress (Ghazizadeh et al., 2021). Indeed, long-term use of psychotropic medicines have previously been associated with a worsening of psychological symptoms (Bertuccioli et al., 2022). Therefore, identifying interventions for those experiencing mild-to-moderate stress will have strong public health implications for the prevention or reduction of symptoms. In addition, an opportunity for dietary supplementation as an over-the-counter option for those who do not wish to take chemical interventions is becoming a popular choice (Ghazizadeh et al., 2021; Bertuccioli et al. 2022).

The current study will employ a parallel, double-blind, randomised placebo-controlled trial, assessing the effect of a single dose intervention of lemon balm extract (or matched placebo) in young-to-middle-aged adults with moderate levels of perceived stress. Subjects will be pre-screened to determine eligibility using the perceived stress questionnaire, where scores between 14 to 26 are indicative of moderate stress, to provide a total of 130 participants. The study comprises a familiarisation visit followed by an acute test day at the Nutritional Psychology Unit based at the University of Reading. The familiarisation visit will allow participants to practice the cognitive battery, complete calmness and mood measures, and provide information on habitual diet (Epic-Norfolk FFQ) and general health and lifestyle patterns to confirm eligibility. On the acute test day, subjective calmness and mood ratings will be recorded at various timepoints throughout the day, beginning with an initial baseline measurement (0h), and then 1h, 3h and 5h after consuming an acute dose of lemon balm extract (300mg) or a matched placebo. At these same timepoints, a computer-based cognitive battery will be completed, consisting of several tasks assessing domains of executive function, attention and memory. On the acute test day participants will arrive fasted and will be provided with a standardised breakfast (two croissants and a glass of water) to be consumed prior to 0h baseline measures. A standardised lunch (cheese sandwich, packet of crisps, and water) will also be provided after the 3h timepoint.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Double-blind

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy, between 18-40 years old
  • Moderate Stress problems (PSS between 14 to 26)
  • No alcohol or vigorous activity 24h before the task
  • No coffee/caffeine intake 12h before the visits
  • Non-smokers or Must not smoke during 7 days prior to the trial: Includes smoking tobacco, vaping nicotine, using nicotine replacement products, or occasional social smoking.
  • Willingness to wash out for food supplementation during 2 weeks before the experiment

排除标准

  • Use medications that may affect the outcome
  • Any long-term psychological or physiological health conditions
  • Have any allergic reactions to ingredients in the capsules
  • Have a BMI greater than or equal to 30
  • Have any allergic reactions to ingredients in the capsules
  • Consumed more than 400 mg of caffeine (>5 expresso) per day in the past 2 weeks
  • Have used any psychotropic medications, stimulants, cannabis, non-registered drug products, or illicit substances in the past 2 weeks, were at risk of drug or alcohol abuse
  • Taking any dietary supplements which they are unwilling to stop for the duration of the study
  • Have sleep disorders or are taking sleep aid medication
  • Fail to demonstrate adequate minimal performance on lab, computer-based cognitive tasks
  • Have a diagnosed neurological condition, or learning/behavioural or neurodevelopmental differences (e.g. dyslexia, autism, ADHD).

结局指标

主要结局

Calmness 9-point Likert Scale

时间窗: 5 hours following intervention

A validated 9-point Likert scale with Calmness Anchor points (CAP) ranging from 1, "Not at all Calm" to 9, "Extremely Calm"

次要结局

  • Subject Satisfaction 4-point Category Scale(5 hours following intervention)
  • Bond-Lader 16-item Visual Analogue Stress Scale(5 hours following intervention)
  • Delayed Word Recall (Rey Auditory Verbal Learning Task)(5 hours following intervention)
  • Modified Attention Network Task (with two blocks of Serial 3's)(5 hours following intervention)
  • Paced Auditory Serial Addition Task(5 hours following intervention)
  • Systolic Blood Pressure(5 hour following intervention)
  • Fatigue 9-point Likert Scale(5 hours following intervention)
  • Diastolic Blood Pressure(5 hours following intervention)
  • Heart Rate(5 hours following intervention)
  • Rapid Visual Information Processing Task(5 hours following intervention)
  • Visual Analogue Stress Scale(5 hours following intervention)
  • Task Switching Test(5 hours following intervention)
  • Immediate Word Recall (Rey Auditory Verbal Learning Task)(5 hours following intervention)

研究者

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

Prof Claire Williams

Chair of Neuroscience

University of Reading

研究点 (2)

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