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Creatine Supplementation and Cognitive and Physical Tests (CREA)

V

Vrije Universiteit Brussel

Status

Completed

Conditions

Healthy
Creatine Supplementation

Treatments

Dietary Supplement: Calcium lactate
Dietary Supplement: Creatine

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To assess whether brain creatine availability has an effect on cognition. To do so we will seek to increase brain creatine concentration via a creatine supplementation protocol.

Enrollment

14 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Healthy (No neurological illness including cardiovascular, renal, and endocrine disorder)
  • Male/female
  • No medication / supplements
  • Non-smoker
  • Low to moderately active
  • Between 18 and 35 years old

Exclusion criteria

  • Injuries
  • Illness
  • Use of medication
  • Use of creatine in the last 3 months
  • History of head trauma or seizure
  • Vegetarian diet [24]
  • Not being able to follow up the restrictions and prohibitions for the subjects (see Restrictions and prohibitions for the subjects)

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

14 participants in 2 patient groups, including a placebo group

Creatine supplementation
Experimental group
Description:
7-day creatine supplementation
Treatment:
Dietary Supplement: Creatine
Placebo supplementation
Placebo Comparator group
Description:
7-day calcium lactate supplementation
Treatment:
Dietary Supplement: Calcium lactate

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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