Short-term Effects of Broccoli-derived Glucoraphanin on Recovery From Eccentric Muscle Damage
SHORT-TERM EFFECTS OF BROCCOLI-DERIVED GLUCORAPHANIN ON RECOVERY FROM ECCENTRIC MUSCLE DAMAGE: A DOUBLE-BLIND RANDOMIZED CROSSOVER STUDY
1 other identifier
interventional
17
0 countries
N/A
Brief Summary
Eccentric exercise induces muscle damage and delay functional recovery. Broccoli-derived glucoraphanin (a sulforaphane precursor that activates Nrf2 defenses) may aid repair; however, its short-term effects in humans remains unknown. This study aims to evaluate whether short-term supplementation with broccoli-derived glucoraphanin will improve recovery from exercise-induced muscle damage. In a randomized, double-blind, placebo-controlled crossover design, fifteen participants will consume either high-glucoraphanin broccoli powder (320 μg) or placebo for one week, followed by elbow flexor eccentric exercise and continued supplementation. Strength, soreness, creatine kinase (CK), range of motion (ROM), arm girths, and ultrasound-assessed muscle and tendon morphology will be measured at baseline, immediately post-exercise, and at 48 and 96 hours post-exercise.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable healthy
Started Feb 2026
Shorter than P25 for not_applicable healthy
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 15, 2025
CompletedFirst Posted
Study publicly available on registry
January 28, 2026
CompletedStudy Start
First participant enrolled
February 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2026
CompletedJanuary 28, 2026
January 1, 2026
28 days
September 15, 2025
January 22, 2026
Conditions
Outcome Measures
Primary Outcomes (3)
Peak torque, Nm/s
Exercise induced damage marker, isokinetic and isometric knee extension
At baseline, immediately post-exercise, and at 48 hours, and at 96 hours post-exercise.
Range of motion, degree
Exercise induced damage marker, elbow extension and flexion
At baseline, immediately post-exercise, and at 48 hours, and at 96 hours post-exercise.
Arm girth, mm
Exercise induced muscle damage marker, arm relaxed and fully flexed
At baseline, immediately post-exercise, and at 48 hours, and at 96 hours post-exercise.
Secondary Outcomes (2)
Soreness, points
At baseline, immediately post-exercise, and at 48 hours, and at 96 hours post-exercise.
Creatine kinase, IU/L
At baseline, immediately post-exercise, and at 48 hours, and at 96 hours post-exercise.
Study Arms (1)
male volunteers aged 18-35 years
EXPERIMENTALInterventions
Participants underwent two separate sessions of muscle-damaging exercise targeting the elbow flexors: (1) following seven days of broccoli powder consumption (condition X), and (2) following an equivalent placebo regimen (condition Y). The broccoli supplementation consisted of 10 g of broccoli powder \[a freeze-dried glucoraphanin-rich broccoli powder (99.5% broccoli and 0.5% mustard seed)\] dissolved in 125 mL of boiling water, providing 320 μg of glucoraphanin per serving. It was consumed when still hot/warm once daily for seven days before and for four days following the eccentric exercise protocol. The placebo powder, matched in appearance and preparation, contained no broccoli-derived bioactives.
The placebo powder, matched in appearance and preparation, contained no broccoli-derived bioactives.
Eligibility Criteria
You may qualify if:
- no resistance training experience in the past 6 months, no arm injuries in the past 2 years, no illnesses in the month prior to data collection, and no known allergies to broccoli or other cruciferous vegetables.
You may not qualify if:
- incomplete participation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- BASIC SCIENCE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
September 15, 2025
First Posted
January 28, 2026
Study Start
February 15, 2026
Primary Completion
March 15, 2026
Study Completion
March 31, 2026
Last Updated
January 28, 2026
Record last verified: 2026-01