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Completed Not applicable Interventional Accepts healthy volunteers

Dose-Response Effects of Short-Term Ashwagandha on Anaerobic Exercise and Cognitive Function in Resistance-Trained Athletes

ClinicalTrials.gov ID: NCT07853274

Public ClinicalTrials.gov record NCT07853274. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 3, 2026, 6:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Dose-Response Effects of Short-Term Ashwagandha Supplementation on Exercise Performance, Resting Energy Expenditure, and Cognitive Function in Resistance-Trained Athletes: A Randomized, Double-Blind, Placebo-Controlled Crossover Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Ashwagandha (ASH) is an herbal supplement derived from the Withania somnifera plant. It is commonly described as an adaptogen, a substance thought to help the body cope with physical and psychological stress. Previous research has examined ashwagandha supplementation using different doses and supplementation periods. This study examined the effects of seven days of supplementation on muscular strength, exercise performance, cognitive function, and selected physiological measures in healthy, resistance-trained men and women. It also examined whether these effects differed between low and high doses. The study used a crossover design in which each participant completed four conditions: no supplementation, a placebo containing maltodextrin, low-dose ashwagandha at 4 mg per kilogram of body weight per day for seven days, and high-dose ashwagandha at 14 mg per kilogram of body weight per day for seven days. The three supplementation conditions were separated by seven-day washout periods. During the blinded supplementation conditions, neither the participants nor the researchers conducting the assessments knew which supplement was being administered. At the end of each seven-day supplementation period, participants completed laboratory assessments. These included the maximum weight lifted for one repetition on the bench press and leg press, total lifting volume across multiple sets, and the speed and power of bar movement. Participants also completed a 30-second all-out cycling sprint to assess anaerobic power, total work, and fatigue, along with a color-word test to assess cognitive performance. Additional assessments included resting energy expenditure, heart rate, blood pressure, perceived exertion, self-reported readiness, focus, alertness, and selected blood markers related to cholesterol, liver function, and muscle damage.

Study identification

NCT ID
NCT07853274
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Enrollment
23 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 40 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 20, 2024 (Actual)
Primary completion
Nov 20, 2024 (Actual)
Completion
Jan 25, 2025 (Actual)
Last update posted
Oct 1, 2026

2024 – 2025

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Exercise Physiology and Nutrition Laboratory (EPNL) at Jacksonville State University Jacksonville Alabama 36265-1724 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07853274, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 1, 2026 · Synced Oct 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT07853274 live on ClinicalTrials.gov.

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