Actively Recruiting

Phase Not Applicable
Age: 18Years - 25Years
FEMALE
Healthy Volunteers
NCT06937190

Pre-Sleep Creatine Enhances Anaerobic Power in Recreationally Active Females

Led by Ankara Yildirim Beyazıt University · Updated on 2025-04-22

24

Participants Needed

1

Research Sites

14 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is a randomized, double-blind, placebo-controlled trial designed to examine the effects of pre-sleep creatine monohydrate supplementation on anaerobic performance and muscle damage markers in recreationally active females. Participants will be randomly assigned to receive either 5 grams of creatine monohydrate or a placebo 30 minutes before sleep for seven consecutive days. Anaerobic performance will be assessed using the Wingate Anaerobic Test, evaluating peak and average power output and fatigue index. Blood samples will be collected before and after the supplementation period to analyze markers of muscle damage, including creatine kinase and lactate dehydrogenase. This study aims to provide insight into the efficacy of short-term, time-specific creatine supplementation for enhancing performance and recovery.

CONDITIONS

Official Title

Pre-Sleep Creatine Enhances Anaerobic Power in Recreationally Active Females

Who Can Participate

Age: 18Years - 25Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Female, aged 18 to 25 years
  • Recreationally active with structured resistance training 3-4 times per week for the past 6 months
  • Regular menstrual cycles for scheduling purposes
  • Able and willing to provide informed consent
  • Agreement to maintain normal diet and training routines throughout the study
Not Eligible

You will not qualify if you...

  • Musculoskeletal injury affecting lower or upper limbs within the past 6 months
  • Known allergy or intolerance to creatine or maltodextrin
  • Use of performance-enhancing substances or supplements within the last 30 days
  • Use of recovery methods such as massage, cryotherapy, or compression garments during the study
  • Current use of anti-inflammatory medication
  • Pregnancy or breastfeeding
  • Inability to comply with study procedures or scheduled assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Islamic Azad University, Shabestar Branch

Shabestar, East Azerbaijan Province, Iran, 5381637183

Actively Recruiting

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Research Team

M

Morteza Jourkesh, PhD

CONTACT

C

Caglar Soylu, phD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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