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Completed

NCT Number: NCT06884566

Effect of Acute Supplementation (taurine) on Maximal Strength and Anaerobic Power

This crossover-design study examines the acute effect of taurine on trained individuals aged 18-40 on strength and power outputs.

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Key information

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Central Lancashire Cyprus

Larnaca, Pyla, 7080, Cyprus

About this study

The purpose of this study is to further investigate any potential ergogenic effects offered by taurine, under specific conditions, namely that of acute supplementation, as opposed to the chronic supplementation protocols of many popular ergogenic aids, such as creatine and beta alanine. Exercise modes investigated include maximal isometric strength, maximal instantaneous power generation, and sustained maximal anaerobic power output, investigated via grip strength, vertical jump height, and the Wingate test, respectively.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • participants 18 - 40 years of age
  • physically active or recreationally active with consistent training more than 3 times per week for at least 6 months
  • non-smokers

Exclusion criteria

  • cardiovascular, respiratory or metabolic diseases
  • any musculoskeletal injury in the last six months
  • taking taurine and/or creatine supplementation in the past three months

Treatment and study plan

Taurine supplementation

Dietary Supplement

For the intervention trials participants consumed the following in randomized order: 50mg·kg -1 of taurine diluted in 500ml of a sugar-free lemonade drink or placebo which was a sugar-free lemonade drink with nothing added, 60 minutes before the exercise protocols. Participants wore a nose plug during consumption to confirm that no taste differences were discernible between trials.

Placebo

Dietary Supplement

For the intervention trials participants consumed the following in randomized order: 50mg·kg -1 of taurine diluted in 500ml of a sugar-free lemonade drink or placebo which was a sugar-free lemonade drink with nothing added, 60 minutes before the exercise protocols. Participants wore a nose plug during consumption to confirm that no taste differences were discernible between trials.

Primary outcomes

  1. Maximal Isometric strength in kilograms assessed via handgrip test

    Time frame: Day 1

  2. Relative Isometric strength in kilograms assessed via handgrip test

    Time frame: Day 1

  3. Maximal Instantaneous power generation in W/kg assessed via vertical jump height test.

    Time frame: Day 1

  4. Average Instantaneous power generation in W/kg assessed via vertical jump height test.

    Time frame: Day 1

  5. Peak power in Watts assessed via the Wingate Anaerobic test

    Time frame: Day 1

  6. Maximal Isometric strength in kilograms assessed via handgrip test

    Time frame: After 48 hours

  7. Relative Isometric strength in kilograms assessed via handgrip test

    Time frame: After 48 hours

  8. Maximal Instantaneous power generation in W/kg assessed via vertical jump height test.

    Time frame: After 48 hours

  9. Average Instantaneous power generation in W/kg assessed via vertical jump height test.

    Time frame: After 48 hours

  10. Peak power in Watts assessed via the Wingate Anaerobic test

    Time frame: After 48 hours

Sponsors and collaborators

Lead sponsor

University of Central Lancashire Cyprus

Other

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Mar 19, 2025
Registry last updated
Mar 19, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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