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The Impacts of Ashwagandha Supplementation on Diurnal Cortisol and Stress Among Women

NCT07647081 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-06-15

No results posted yet for this study

Summary

The purpose of this project is to better understand the role of ashwagandha on the stress response and wellbeing among healthy, stressed women.

Conditions

  • Stress

Interventions

OTHER

Placebo

Brown Rice Powder

DIETARY_SUPPLEMENT

KSM-66 Ashwagandha

600mg daily KSM-66 Ashwagandha

Sponsors & Collaborators

  • Oklahoma State University Center for Health Sciences

    lead OTHER

Principal Investigators

  • Julie Croff, PhD · Oklahoma State University Center for Health Sciences

  • Erica Crockett, MPH · Oklahoma State University Center for Health Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-06-30
Primary Completion
2026-12-31
Completion
2027-05-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07647081 on ClinicalTrials.gov