NCT07373106

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

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
17

participants targeted

Target at below P25 for not_applicable healthy

Timeline
Completed

Started Feb 2026

Shorter than P25 for not_applicable healthy

Status
not yet recruiting

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

September 15, 2025

Completed
5 months until next milestone

First Posted

Study publicly available on registry

January 28, 2026

Completed
18 days until next milestone

Study Start

First participant enrolled

February 15, 2026

Completed
28 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 15, 2026

Completed
16 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2026

Completed
Last Updated

January 28, 2026

Status Verified

January 1, 2026

Enrollment Period

28 days

First QC Date

September 15, 2025

Last Update Submit

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

EXPERIMENTAL
Dietary Supplement: broccoli powder consumptionDietary Supplement: Placebo (no broccoli-derived bioactives)

Interventions

broccoli powder consumptionDIETARY_SUPPLEMENT

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.

male volunteers aged 18-35 years

The placebo powder, matched in appearance and preparation, contained no broccoli-derived bioactives.

male volunteers aged 18-35 years

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

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