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CompletedNCT07877441Updated Oct 16, 2026

Antioxidant Supplementation and Muscle Recovery From DOMS in Trained Women

An interventional study of Creatine Monohydrate and Omega 3 FA (Fish Oil) in Delayed Onset Muscle Soreness, Exercise-induced Muscle Damage and Muscle Recovery, sponsored by Antonio Molina Lopez. Completed at 1 site in Spain. Open to female participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Antonio Molina Lopez · Not applicable, Interventional, and Basic science

From the registry’s dates

  • Registered 7 months after the study started (first participant enrolled Feb 2026, registered Oct 2026).
Updated Oct 16, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

This randomized, placebo-controlled, parallel-group trial investigated the effects of combined antioxidant and anti-inflammatory supplementation on delayed onset muscle soreness (DOMS) recovery in trained women. Sixty trained women (18-35 years) were randomized into four groups: G1 (Creatine + Omega-3), G2 (Creatine + Omega-3 + NAC), G3 (Creatine + Omega-3 + NAC + CoQ10), and G4 (Placebo). Outcomes included muscle pain pressure threshold, countermovement jump, handgrip strength, 30-meter sprint, bilateral dynamometry, infrared thermography, creatine kinase, and heart rate variability, assessed before and after an eccentric exercise protocol.

Read the detailed description

Delayed onset muscle soreness (DOMS) is a common physiological response to eccentric exercise, characterized by muscle pain, reduced force production, and impaired neuromuscular function. Antioxidant and anti-inflammatory compounds such as creatine, omega-3 fatty acids, N-acetylcysteine (NAC), and coenzyme Q10 (CoQ10) have been proposed as potential modulators of exercise-induced muscle damage. This study used a 4-arm parallel RCT design with participant and assessor blinding. Participants underwent a standardized eccentric exercise protocol to induce DOMS, followed by 72 hours of monitoring. Measurements were taken at baseline (T1), post-exercise (T2), 24h (T3), 48h (T4), and 72h (T5) post-exercise. Analysis of covariance (ANCOVA) was performed with baseline values and age as covariates.

02

Conditions studied

  • Delayed Onset Muscle Soreness
  • Exercise-induced Muscle Damage
  • Muscle Recovery

Keywords

  • DOMS
  • ANTIOXIDANT SUPPLEMENTATION
  • ECCENTRIC EXERCISE
  • TRAINED WOMEN
  • MUSCLE RECOVERY
  • RANDOMIZED CONTROLLED TRIAL
03

In context

Lead sponsor

Antonio Molina Lopez is the lead sponsor of 3 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Female sex
  • Age 18-35 years
  • Trained status (regular resistance or sport training)
  • Enrolled at Universidad Europea de Madrid
  • Absence of musculoskeletal injury at time of recruitment
  • No use of anti-inflammatory drugs or nutritional supplements in the 4 weeks prior to the study

Exclusion criteria

Exclusion Criteria:

  • History of chronic musculoskeletal or cardiovascular disease
  • Use of anti-inflammatory medication or antioxidant supplementation in the prior 4 weeks
  • Pregnancy or breastfeeding
  • Inability to complete the eccentric exercise protocol
  • Non-compliance with supplementation or dietary control requirements
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    G1: Creatine + Omega-3

    Participants received creatine monohydrate (5 g/day) combined with omega-3 fish oil (2 capsules/day; 456 mg EPA + 225 mg DHA per capsule) for 4 weeks. The final week coincided with the 5 assessment timepoints following the eccentric exercise protocol to induce DOMS.

    Dietary Supplement: Creatine Monohydrate · Dietary Supplement: Omega 3 FA (Fish Oil)

  • Experimental
    G2: Creatina + Omega-3 + NAC

    Participants received creatine monohydrate (5 g/day), omega-3 fish oil (2 capsules/day; 456 mg EPA + 225 mg DHA), N-acetylcysteine (600 mg/day) for 4 weeks. The final week coincided with the 5 assessment timepoints following the eccentric exercise protocol to induce DOMS.

    Dietary Supplement: Creatine Monohydrate · Dietary Supplement: Omega 3 FA (Fish Oil) · Dietary Supplement: N-Acetyl Cysteine (NAC)

  • Experimental
    G3: Creatina + Omega-3 + NAC + CoQ10

    Participants received creatine monohydrate (5 g/day), omega-3 fish oil (2 capsules/day; 456 mg EPA + 225 mg DHA), N-acetylcysteine (600 mg/day), and coenzyme Q10 (100 mg/day) for 4 weeks. The final week coincided with the 5 assessment timepoints following the eccentric exercise protocol to induce DOMS.

    Dietary Supplement: Creatine Monohydrate · Dietary Supplement: Omega 3 FA (Fish Oil) · Dietary Supplement: N-Acetyl Cysteine (NAC) · Dietary Supplement: Coenzyme Q10 100 MG Oral Capsule

  • Experimental
    G4: Placebo

    Participants received a placebo consisting of maltodextrin (5 g/day) and olive oil capsules (2 capsules/day), visually identical to the active arms in capsule size, sachet format, and packaging colour, for 4 weeks.

    Dietary Supplement: Placebo

Interventions

  • Dietary supplementCreatine Monohydrate

    Creatine monohydrate administered at 5 g/day for 4 weeks. Used in G1, G2, and G3 arms

  • Dietary supplementOmega 3 FA (Fish Oil)

    Administered as 2 capsules/day (456 mg EPA + 225 mg DHA per capsule; EPA:DHA ratio 2:1) for 4 weeks. Included in G1, G2, and G3 arms.

  • Dietary supplementN-Acetyl Cysteine (NAC)

    Administered at 600 mg/day for 4 weeks. Included in G2 and G3 arms.

  • Administered at 100 mg/day for 4 weeks. Included in G3 arm only.

  • Dietary supplementPlacebo

    Maltodextrin (5 g/day) and olive oil capsules (2 capsules/day), visually identical to active arms. Administered for 4 weeks in G4 arm.

06

What researchers measure

Primary outcomes

  1. Countermovement Jump Height (CMJ)

    Assessed using My Jump Lab app (240 fps). Jump height in centimeters as indicator of lower limb neuromuscular performance recovery

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  2. Muscle Pain Pressure Threshold

    Assessed using a pressure algometer (BASELINE). Measures the minimum pressure at which the participant perceives pain, expressed in kg/cm²

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  3. 30- Meter Sprint Time

    Assessed using Witty photocell system (Microgate). Time in seconds to complete a 30-meter sprint.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  4. Creatine Kinase (CK)

    ssessed using SimplexTAS 101 analyzer. Serum CK activity in U/L as a biochemical marker of muscle damage.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

Secondary outcomes

  1. RIGHT LEG DYNAMOMENTRY

    Assessed using Activforce 2 dynamometer. Maximum isometric knee extension force in kg.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  2. LEFT LEG DYNAMOMETRY

    Assessed using Activforce 2 dynamometer. Maximum isometric knee extension force in kg.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  3. Thermography

    Assessed using FLIR T2 A315 thermographic camera. Skin temperature of the quadriceps region in degrees Celsius as marker of local inflammation.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

  4. Heart Rate Variability

    Assessed using Polar Team Pro chest straps. 5-minute supine recording with eyes closed and deep breathing. Root mean square of successive differences in ms as autonomic recovery indicator.

    Time frame: Baseline (Day 0), immediately post-exercise (Day 2), 24 hours after exercise (Day 3), 48 hours after exercise (Day 4), and 72 hours post-eccentric exercise (Day 5)

07

Study locations

1 site
  • Diego
    Madrid, Spain
08

References and documents

Individual participant data

Plan to share: Yes — Individual participant data (IPD) that underlie the results reported in the published article, after de-identification, will be made available upon reasonable request to the corresponding author. Data will include all outcome variables assessed at each time point (T1-T5) for all 60 participants. Requests should be directed to the corresponding author and will be considered on a case-by-case basis following publication.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2026 to primary completion in Apr 2026, 2 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 5, 2026
First posted
Oct 16, 2026
StartActual
Feb 19, 2026
Primary completionActual
Apr 23, 2026
CompletionActual
Apr 23, 2026
Last update
Oct 16, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07877441
Lead sponsor
Antonio Molina Lopez
Collaborators
NUTRIFARMA, Unifarco SpA
Responsible party
Antonio Molina Lopez (Co-Investigator, Universidad Pablo de Olavide) — Sponsor-investigator
First posted
Oct 16, 2026
Start date
Feb 19, 2026
Primary completion
Apr 23, 2026
Completion
Apr 23, 2026
Last update
Oct 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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Studies of the drugs tested here: Creatine monohydrate · Fish Oils · Acetylcysteine · Coenzyme Q10

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