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Pre-Sleep Creatine Enhances Anaerobic Power in Recreationally Active Females

Pre-Sleep Creatine Enhances Anaerobic Power in Recreationally Active Females

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06937190
Acronym
SleepCrM
Enrollment
24
Registered
2025-04-22
Start date
2025-04-01
Completion date
2025-07-10
Last updated
2025-04-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaerobic Performance, Sports Nutrition, Exercise Recovery, Muscle Fatigue, Creatine Supplementation, Recreational Physical Activity, Female Athletes

Keywords

Creatine Monohydrate, Pre-Sleep Supplementation, Anaerobic Power, Wingate Test, Muscle Damage Markers, Creatine Kinase (CK), Lactate Dehydrogenase (LDH), Female Exercise Performance, Nutritional Ergogenic Aid, Resistance Training, Recovery Enhancement

Brief summary

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.

Interventions

DIETARY_SUPPLEMENTCreatine Monohydrate

Participants will receive 5 grams of creatine monohydrate powder dissolved in water, flavored with a sugar-free agent, 30 minutes before sleep each night for 7 days.

DIETARY_SUPPLEMENTPlacebo (Maltodextrin)

Visually identical placebo (maltodextrin powder, 5 g/day), flavored with a sugar-free agent, dissolved in water and consumed 30 minutes before sleep for 7 consecutive days.

Sponsors

Ankara Yildirim Beyazıt University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Neither the participants nor the investigators know which intervention the participant is receiving.

Intervention model description

Participants are randomly assigned to one of two groups: a creatine supplementation group or a placebo group, and they remain in that group for the duration of the trial.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

Female, aged 18 to 25 years Recreationally active (engaging in structured resistance training 3-4 times per week for the past 6 months) Regular menstrual cycles (used for scheduling purposes) Able and willing to provide informed consent Agreement to maintain normal diet and training routines throughout the study

Exclusion criteria

History of 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 modalities such as massage, cryotherapy, or compression garments during the study period Current use of anti-inflammatory medication Pregnancy or breastfeeding Inability to comply with study protocol or scheduled assessments

Design outcomes

Primary

MeasureTime frameDescription
Average Power Output (Watts) - 30-Second Wingate TestBaseline and post-intervention (Day 0 and Day 7)Average anaerobic power output will be calculated across the 30-second Wingate cycling test.

Secondary

MeasureTime frameDescription
Peak Power Output (Watts) - Wingate TestBaseline and post-intervention (Day 0 and Day 7)Peak power output during the initial 5 seconds of the 30-second Wingate cycling test.
Fatigue Index (%) - Wingate TestBaseline and post-intervention (Day 0 and Day 7)Calculated as the percent drop in power from peak to minimum power output during the 30-second Wingate test, indicating fatigue rate.
Serum Creatine Kinase (CK) ActivityBaseline and 24 hours post Wingate Test (Day 0 and Day 8)Serum creatine kinase activity will be measured as a marker of muscle damage using a spectrophotometric assay.
Serum Lactate Dehydrogenase (LDH) ActivityBaseline and 24 hours post Wingate Test (Day 0 and Day 8)Serum lactate dehydrogenase activity will be measured as an indicator of cell membrane permeability and muscle damage using spectrophotometry.

Countries

Iran

Contacts

Primary ContactMorteza Jourkesh, PhD
mjourkesh@iau.ac.ir+98 938 278 4093
Backup ContactCaglar Soylu, phD
fztcaglar5187@gmail.com+90 5078593595

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026