Herbal Tincture for Stress, Anxiety, and Sleep Quality
This study aims to evaluate whether an herbal tincture can improve sleep quality and mental well-being in adults experiencing stress and anxiety.
Alcohol Alternative Herbal Tincture (Test Product)
+ Placebo
Anxiety Disorders+4
+ Mental Disorders
+ Sleep Initiation and Maintenance Disorders
Treatment Study
Summary
Study start date: May 9, 2024
Actual date on which the first participant was enrolled.This study is focused on finding out whether a herbal tincture can help people who have problems with sleep, stress, and anxiety. The research aims to see if this alternative treatment can improve sleep quality, create a calming effect, and reduce stress and anxiety symptoms. It involves 80 people who often experience such issues. Understanding if this herbal remedy works could provide a new option for those looking for natural ways to manage their stress and improve their sleep. Participants in this virtual study will be randomly assigned to either receive the herbal tincture or a placebo, without knowing which one they are taking, to ensure unbiased results. The trial lasts for eight weeks, during which time participants will use a sleep tracker and complete personalized questionnaires to monitor changes in their sleep patterns and stress levels. This setup helps researchers accurately measure the tincture's effectiveness in promoting better sleep and reducing stress and anxiety. The study is designed to ensure the safety and anonymity of all participants involved.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 21 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location