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Promoting cognitive health in physically active older adults: the role of Creatine and Strength Training over 12 weeks

MedEpiGen Project: Preventive Medicine for Metabolic Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5czhc4k
Enrollment
Unknown
Registered
2025-10-17
Start date
2023-01-20
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Cognitive Dysfunction

Interventions

This study is a randomized, controlled, parallel, double-blind clinical trial. Participants will be randomly assigned to four groups: (1) resistance training combined with creatine supplementation, (2

Sponsors

Programa de Pós-Graduação em Genética da Universidade Federal do Paraná
Lead Sponsor
Universidade Estadual do Centro Oeste
Collaborator

Eligibility

Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Be regular exercisers for at least 12 months. Comply with the physical activity recommendations of the World Health Organization (WHO). Have medical clearance to take part in the study. Controlled blood pressure, no metabolic or endocrine disorders. Zero score on the cognitive assessment (CDR). Have attended regular school for at least 4 years. Aged 60 or over. Both sexes

Exclusion criteria

Exclusion criteria: Missing a training session without making up for it. Any falls that compromise exercise. Presenting metabolic, endocrine or renal disorders after starting the program, detected during a routine consultation with the general practitioner. Need for intervention with any type of medication not listed above. Cognitive assessment (Clinical Dementia Rating - CDR) with a result higher than zero

Design outcomes

Primary

MeasureTime frame
The combination of strength training and creatine supplementation is expected to improve the cognitive capacity of physically active elderly people.

Secondary

MeasureTime frame
No secondary outcomes are expected.

Countries

Brazil

Contacts

Public ContactGabriel Cordeiro

Universidade Estadual do Centro Oeste

ppgdc@unicentro.br+55(42) 3421-3114

Outcome results

None listed

Source: REBEC (via WHO ICTRP)