Skip to content

strong cctive mind Project - strength exercises to improve the cognition of older women

Adaptations of cognitive, muscular, functional and sedentary behavior induced by Strength Training with and without blood flow restriction in older women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-7bc8zp
Enrollment
Unknown
Registered
2019-09-19
Start date
2019-12-03
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

Healthy volunteers

Interventions

Intervention Groups: Those selected to participate in one of the 4 study groups: (G1) Moderate intensity strength training (15RM) (n = 12), (G2) Low intensity strength training (30 RM) (n = 12) and (G
Other
G11.427.410.698.277
E02.760.169.063.500.387.875

Sponsors

Universidade Federal da Paraíba
Lead Sponsor
Universidade Federal da Paraíba
Collaborator

Eligibility

Sex/Gender
Female
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: The eligibility criteria for the evaluation of the subjects will be, women; between 60 and 80 years old; apparently healthy, without osteo-articular problems in the upper and lower limbs, contraindicated for strength exercises; physically active; no history of previous cardiovascular, neurological or psychiatric diseases, controlled hypertension; no history of traumatic brain injury with loss of consciousness for more than 30 minutes; non-alcoholic and non-smokers; absence of uncorrected motor, visual and auditory impairment; have completed elementary school education or higher; no Brachial Ankle Index, less than 0.90 and greater than 1.40, which characterizes a sign of peripheral arterial disease; have not participated in strength training for at least 6 months; present value above 24 in the Mini Mental State Examination questionnaire

Exclusion criteria

Exclusion criteria: The exclusion criteria adopted will be regular non-follow-up in training sessions and any test phase with absence in training exceeding 25 percent of total sessions

Design outcomes

Primary

MeasureTime frame
Assess cognitive function through the tests: Mini Mental State Examination, Stroop Word-Color, Digit Span B & F, TMT - AB and Verbal Fluency test, measured before and after 16 weeks of intervention.

Secondary

MeasureTime frame
It is expected to find an increase in trophic factor BDNF, measured by blood analysis;It is expected to find an improvement in Functional Performance (Strength, Speed, Agility and Balance) as measured by the sit-and-stand test, usual speed and top speed, time up and go test and dynamic balance test;It is expected to find an improvement in the psychological variables (anxiety, depression) and sleep quality, measureds through questionnaires;It is expected to find an increase in physical activity level and decrease in sedentary behavior, measured by accelerometer;It is expected to find an increase in muscle strength, measured by the 1 RM test, measured before and after 16 weeks of the intervention;Maintenance or improvement of the performance of dual tasks (motor and cognitive; motor-motor and double-motor and cognitive), measured by motor and cognitive tests, before and after 16 weeks of the intervention;Static and dynamic balance improvement, measured through the balance platform, measured before and after 16 weeks of intervention.;Improvement in brain activation, measured by portable EEG (MUSE headband) before and after 16 weeks of intervention.;Improvement of body composition, measured by bioimpedance, before and after 16 weeks of intervention.

Countries

Brazil

Contacts

Public ContactJoamira Araujo

Universidade Federal da Paraíba

joamira@ifce.edu.br+55-88-98804-2439

Outcome results

None listed

Source: REBEC (via WHO ICTRP)