Dose-Response Effects of Short-Term Ashwagandha on Anaerobic Exercise and Cognitive Function in Resistance-Trained Athletes
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.
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
Conditions
Interventions
- Low-dose Ashwagandha Supplement Dietary Supplement
- High-dose Ashwagandha Supplement Dietary Supplement
- Maltodextrin (Placebo) Dietary Supplement
Dietary Supplement
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.