A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffects.
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 60
- 试验地点
- 2
- 主要终点
- Reduction in Symptoms Associated with Alcohol Aftereffects
研究概览
简要总结
This study assesses the effectiveness of JoyRise Recovery Powder in reducing alcohol aftereffects, cognitive impairment, and anxiousness among participants aged 35-54 who consume alcohol. Participants will be randomly assigned to either the JoyRise group or a placebo group. The study will measure hangover symptoms, cognitive function, and overall well-being through a series of questionnaires and cognitive tests at baseline, 30 minutes after product consumption, and 4 hours later.
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
- Double (Participant, Investigator)
盲法说明
This study uses a double-blind design, meaning that both the participants and the investigators are unaware of the group assignments.
入排标准
- 年龄范围
- 35 Years 至 54 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Aged 35-54, male or female
- •Regular alcohol consumption
- •Event planned within one month that involves alcohol consumption
- •Willingness to avoid new medications or supplements during the study period
- •Must confirm that they will not drive while under the influence of alcohol.
排除标准
- •Anyone not in good health.
- •Anyone who has any chronic health conditions such as oncological or psychiatric disorders.
- •Anyone who has any known serious allergic reactions that require the use of an Epi-Pen.
- •Anyone who is pregnant, breastfeeding, or trying to conceive.
- •Anyone who cannot/ will not commit to the study protocol.
- •Anyone with a history of substance abuse.
- •Anyone who has undergone an invasive medical procedure in the six months prior to the study, or has a procedure planned during the study duration.
- •Anyone currently using any medications that may affect their response to alcohol or impact hangover symptoms, such as diuretics (water pills) or medication for hypertension.
- •History of severe reactions or sensitivity to alcohol.
- •Anyone currently taking glutathione.
结局指标
主要结局
Reduction in Symptoms Associated with Alcohol Aftereffects
时间窗: Baseline and 30 minutes after product consumption on the day following alcohol consumption.
Measurement of the reduction in alcohol aftereffects using the Alcohol Hangover Questionnaire (AHQ). Participants will self-report their symptoms, such as headache, nausea, and tiredness.
次要结局
- Reduction in Feelings of Anxiousness(Baseline and 30 minutes after product consumption on the day following alcohol consumption.)
- Increased User Satisfaction with Overall Well-being(Baseline and 4+ hours after product consumption on the day following alcohol consumption.)
- Improvement in Cognitive Function(Baseline and 30 minutes after product consumption on the day following alcohol consumption.)