Ashwagandha Supplementation for Prevention of Muscle Damage
1 other identifier
interventional
19
1 country
1
Brief Summary
Ashwagandha is an herbal supplement that has a wide range of benefits related to exercise when supplemented for about 8-12 weeks. This study aims to investigate whether short-term Ashwagandha supplementation can enhance muscle recovery following exercise by measuring muscle strength recovery, swelling, and soreness in the biceps.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 15, 2025
CompletedStudy Start
First participant enrolled
March 22, 2025
CompletedFirst Posted
Study publicly available on registry
March 28, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
May 15, 2025
CompletedFebruary 23, 2026
February 1, 2026
1 month
March 15, 2025
February 19, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Change in isometric biceps strength measured with a dynamometer (Nm)
72 hours
Secondary Outcomes (3)
Change in muscle thickness measured with ultrasound (cm)
72 hours
Change in muscle soreness measured with a visual analog scale with scores ranging from 0 (no soreness) to 10 (maximal soreness)
72 hours
Change in sleep quality with the Pittsburgh Sleep Quality Index with scores ranging from 0 (no sleep problems) to 3 (lowest sleep quality)
10 days
Study Arms (2)
Placebo
PLACEBO COMPARATOR600 mg/d placebo for 10 days
Ashwagandha
EXPERIMENTAL600 mg/d Ashwagandha
Interventions
Eligibility Criteria
You may not qualify if:
- Conditions that may be affected by exercise (determined by "yes" answers to the "Get Active Questionnaire") Pregnant Breastfeeding
- Allergies to:
- Dicalcium Phosphate
- Cellulose
- Vegetable magnesium stearate
- Silica
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Saskatchewan
Saskatoon, Saskatchewan, S7K 2X2, Canada
MeSH Terms
Interventions
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
March 15, 2025
First Posted
March 28, 2025
Study Start
March 22, 2025
Primary Completion
April 30, 2025
Study Completion
May 15, 2025
Last Updated
February 23, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share