NCT07540858

Brief Summary

In this study, we investigated the impact of a comprehensive microgreen and wheatgrass juice protocol on the miRNA response following a standardized EIMD model and whether microgreen consumption could modulate key miRNA markers of neuromuscular regeneration and metabolic adaptation, thereby offering a novel nutritional approach to enhancing holistic recovery in athletes.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
3mo left

Started May 2026

Shorter than P25 for not_applicable

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

April 15, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

April 20, 2026

Completed
22 days until next milestone

Study Start

First participant enrolled

May 12, 2026

Expected
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 12, 2026

2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Last Updated

April 20, 2026

Status Verified

April 1, 2026

Enrollment Period

1 month

First QC Date

April 15, 2026

Last Update Submit

April 15, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Muscle recovery related miRNAs

    Real time PCR expressions of serum miRNAs

    From enrollment to the end of treatment at 12 weeks

Study Arms (2)

Microgreen

EXPERIMENTAL

Microgreen received group

Dietary Supplement: Microgreens

control

PLACEBO COMPARATOR

not received microgreens

Other: not received any supplement

Interventions

MicrogreensDIETARY_SUPPLEMENT

Participants received microgreens for 21 days

Microgreen

This group will not receive any dietary supplement

control

Eligibility Criteria

Age19 Years - 24 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Central Study Contacts

Mahmut Açak, Professor

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PROFESSOR

Study Record Dates

First Submitted

April 15, 2026

First Posted

April 20, 2026

Study Start (Estimated)

May 12, 2026

Primary Completion (Estimated)

June 12, 2026

Study Completion (Estimated)

July 30, 2026

Last Updated

April 20, 2026

Record last verified: 2026-04

Data Sharing

IPD Sharing
Will not share