A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffe… (NCT06575972) | Clinical Trial Compass
CompletedNot Applicable
A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffects.
United States60 participantsStarted 2024-06-25
Plain-language summary
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.
Who can participate
Age range35 Years – 54 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* 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.
Exclusion Criteria:
* 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.
What they're measuring
1
Reduction in Symptoms Associated with Alcohol Aftereffects
Timeframe: Baseline and 30 minutes after product consumption on the day following alcohol consumption.