A Clinical Study to Assess the Effects of JoyRise Recovery Powder on Mitigating Alcohol Aftereffects.

Completed · Not applicable · Has a placebo group

Conditions studied: Alcohol Aftereffects, Anxiety, Cognitive Impairment

In brief

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.

Key facts

Study ID
NCT06575972
Run by
Joyrise
People needed
60
Starts
2024-06-25
Expected to finish
2024-08-01
Last updated by the study team
2024-08-28

Who can join

Age: 35 and older, up to 54. Sex: any. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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