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The effect of Creatine adjunct on Athletes Mood and Affect.

Evaluation of the Creatine adjunct effect on athletes mood and affect in body building clubs: a randomized clinical trial

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015040521609N1
Enrollment
44
Registered
2015-06-27
Start date
2013-12-12
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Psychiatric conditions. Depression

Interventions

Intervention 1: In the intervention group, the athletes were received 5 gram Creatine Monohydrate (from Karen pharmaceutical company) in 7 capsules, administered orally, daily for 6 weeks. Interventio
Treatment - Drugs
Placebo
In the intervention group, the athletes were received 5 gram Creatine Monohydrate (from Karen pharmaceutical company) in 7 capsules, administered orally, daily for 6 weeks.
The placebo group received wheat flour capsule (7 capsules daily) for the same time (6 weeks) and the same appearance (Creatine capsule) in intervention group.

Sponsors

Vice chancellor for research of Iran university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: age between 16-60, male gender; regular daily physical exercise; not having history of allergy to Creatine; not having history of medical disease such as heart disease, renal disorder, thyroid disease or cancer; not having history of psychiatric drug consumption or OTC usage or drug and alcohol abuse during past 3 months; not having history of axis 1 psychiatric disorders. Exclusion criteria: allergy to Creatine; any medical complication during the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
The score of mood. Timepoint: Before the intervention, 3 weeks after begining of intervention, 6 weeks after begining of intervention. Method of measurement: Beck depression scale.;The score of affect. Timepoint: Before the intervention, 3 weeks after begining of intervention, 6 weeks after begining of intervention. Method of measurement: PANAS questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehrdad Eftekhar

Iran university of medical sciences

mehrdad.eftekhar@gmail.com+98 21 6405 3312

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026