Effects of Ashwagandha Extract on Stress Levels

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Stress

In brief

The purpose of this study is to evaluate the efficacy of two proprietary ashwagandha extracts on stress levels, with secondary outcomes of cognition, energy, and sleep, as compared to a placebo.

Key facts

Study ID

NCT06793891

Run by

Nutraceuticals Research Institute

People needed

60

Starts

2024-10-21

Expected to finish

2025-04-30

Last updated by the study team

2025-01-27

Who can join

Age: 30 and older, up to 59. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Provision of signed and dated informed consent form
• Stated willingness and demonstrated ability to comply with all study procedures, as well as availability for the duration of the study
• Self reported high stress
• Baseline score of above-average stress levels on the NRI-SS
• Biological sex of woman; gender identification of female
• Aged 30 to 59, inclusive
• Good general health as evidenced by medical history and screening
• For females of reproductive potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation and for an additional month after the end of the study
• Agreement to adhere to Lifestyle Considerations throughout study duration

You may not qualify if…

• Pregnancy, trying to conceive, or breastfeeding
• Currently smokes or vapes (i.e., tobacco, flavored items, marijuana, etc.) or has in the past year
• Consumes > 8 alcoholic beverages in an average week
• Is a primary caretaker for a child younger than 18 months of age
• Currently consumes an ashwagandha supplement or has consumed one regularly (defined as 1x week or more often) within the past 24 months
• Consumes any stress aid, medication, diet, or supplement intended to improve stress in any way
• Current or recent (within 60 days) history of taking thyroid medications, hypertensive drugs, CNS depressants, diabetic medications, benzodiazepines, or immunosuppressants
• Any liver or kidney disorder
• Known allergic reactions to any components of the intervention
• Positive COVID-19 test within 30 days of the study period
• Recent dramatic weight changes (10% change in body weight in the last 6 months)
• Introducing a new investigational drug or other intervention within 60 days before the start of the study
• Introducing a new lifestyle stress-reduction aid (i.e. physical activity, yoga, etc) within 60 days before the start of the study

Where it is running

• Nutraceuticals Research Institute — Huntsville, Alabama, United States (enrolling)

Full record on ClinicalTrials.gov

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