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Study identifier: NCT07441070 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of Ashwagandha Root Extract on Stress, Anxiety, and Sleep Quality in Adults Experiencing Minority Stress

Condition: Minority Stress · Psychological Stress · Anxiety  ·  Sponsor: SF Research Institute, Inc.

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to 45 Years
Healthy volunteersYes

About this study

Sexual and gender minority adults often experience elevated levels of chronic stress due to stigma, discrimination, and social adversity, commonly referred to as minority stress. This persistent stress is associated with increased anxiety, mood disturbances, impaired sleep quality, and reduced quality of life. There is a need for safe, non-pharmacological interventions that can support mental well-being in this population. This randomized, double-blind, placebo-controlled study is designed to evaluate the efficacy and safety of Ashwagandha (Withania somnifera) root extract in reducing stress and improving anxiety and sleep quality in adults experiencing minority stress. A total of 80 adults aged 18 to 45 years who self-identify as sexual or gender minorities and report moderate to high perceived stress will be enrolled. Participants will be randomly assigned to receive either Ashwagandha root extract (300 mg capsules taken twice daily) or an identical placebo for 8 weeks. Efficacy will be assessed using validated psychological and quality-of-life questionnaires, including the Perceived Stress Scale, Depression Anxiety Stress Scale, Pittsburgh Sleep Quality Index, and other mood and minority stress measures. Salivary cortisol will be measured as a biological marker of stress. Safety will be evaluated through monitoring of adverse events throughout the study.

This description comes directly from the study's public registry record.

Talk to the study team

Dr. John Ademola  ·  415-845-4638  ·  jademola@sfinstitute.com

Always discuss trial participation with your own doctor first.

Locations (1)

San Francisco Research InstituteSan Francisco, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07441070