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临床试验/NCT06697847
NCT06697847已完成不适用

Assessing Taste Thresholds and Scores on Standardised Mood Questionnaires in Participants Without Mood Disorders

Ranvier Health Ltd1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年11月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
Sweet taste threshold

研究概览

简要总结

The sweet threshold (concentration of sucrose in water) at which healthy participants can detect a sweet flavour will be recorded.

详细描述

The sweet threshold (concentration of sucrose in water) at which healthy participants can detect a sweet flavour will be recorded by means of application on a cotton bud to the anterior third of the tongue. Solutions will be presented in a pseudo-randomised order. Mood questionnaires will be completed (to check that participants are indeed healthy). The questionnaires used will be the Patient Health Questionnaire 9 (PHQ9), Beck's Depression Inventory (BDI) and Generalised Anxiety Disorder Questionnaire 7 (GAD-7).

This data is being collected with the intention of its use for comparison with sweet thresholds established in other populations using the same method of sweet threshold estimation.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

入排标准

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

入选标准

  • •. Male and female adults of 18 years old and over;
  • •Participants without a diagnosis of major depressive disorder (MDD) / anxiety disorder;
  • •Participants not taking an antidepressant during the preceding 6 months
  • •Not suffering from significant other mental or physical illness, such as confirmed psychosis, end of life care, or any other condition assessed as significant by the Site Investigator;
  • •Willing and able to comply with all study-related procedures;
  • •Not having COVID 19 or continuing effects of COVID 19 including altered sense of taste;
  • •Understands the study requirements and the treatment procedures and is able to provide written informed consent.

排除标准

  • •Taking antidepressant medication currently or during the previous 6 months;
  • •Known or suspected hypersensitivity or intolerance to any taste testing solutions, or any of their excipients;
  • •A history or presence of neurological or confounding psychiatric conditions (such as stroke, traumatic brain injury, epilepsy, space occupying lesions, multiple sclerosis, Parkinson's disease, vascular dementia, transient ischemic attack, or schizophrenia);
  • •Patients with a diagnosis of chronic pain;
  • •Pregnancy or possibility pregnancy, or breastfeeding;
  • •Participants using supplements containing psychoactive herbs (for example St Johns Wort or 5-HTP (5-Hydroxytryptophan, also known as oxitriptan);
  • •Participants regularly using psychoactive stimulants (for example MDMA);
  • •Participants unable or unwilling to comply with study procedures.

研究组 & 干预措施

Healthy volunteers

Adults with no mood disorder and who have not been diagnosed with or had treatment for a mood disorder in the last 6 months.

结局指标

主要结局

Sweet taste threshold

时间窗: From enrolment to a final taste test 6 weeks later

Sweet taste threshold established by applying varying concentrations of sucrose solution to the tongue and assessing whether a sweet taste can be detected by the participant. The sweet threshold is the minimum concentration at which a participant can reliably detect the sweet flavour.

次要结局

  • Score on Becks Depression Inventory(From enrolment to a final questionnaire 6 weeks later)
  • Score on Patient Health Questionnaire 9(From enrolment to a final questionnaire 6 weeks later)
  • Score on Generalised Anxiety Disorder scale 7(From enrolment to a final questionnaire 6 weeks later)

研究者

发起方
Ranvier Health Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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