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Fatigability and Physical Performance: Effects of Resistance Training Variables Manipulation

Fatigability and Physical Performance: Effects of Resistance Training Variables Manipulation

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03619070
Enrollment
80
Registered
2018-08-07
Start date
2018-05-20
Completion date
2018-11-15
Last updated
2018-08-08

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

Conditions

Aging

Keywords

Fatigability, Postmenopausal Woman, Resistance training, Physical performance, Older adults

Brief summary

This study evaluate whether resistance training variables modulate the fatigability (power-duration relationship) and physical performance in adults and older adults

Detailed description

The resistance training variables manipulation is utilized for maximize the results of resistance training. However it is unclear whether the resistance training variables manipulation modulates the fatigability (i.e. power-duration relationship) and whether this explains the improvement on physical performance (i.e. gait speed, sit-to-stand and timed up and go tests).

Interventions

OTHERResistance training, LL

In LL, the postmenopausal women will be submitted to 12 weeks of Resistance training with moderate volume (i.e. three sets per exercise) and low load (i.e. 30% of one repetition maximum)

OTHERResistance training, HL

In HL, the postmenopausal women will be submitted to 12 weeks of Resistance training with moderate volume (i.e. three sets per exercise) and high load (i.e. 80% of one repetition maximum)

OTHERResistance training, HVHL

In HVHL, the postmenopausal women will be submitted to 12 weeks of Resistance training with high volume (i.e. six sets per exercise) and hig load (i.e. 80% of one maximum repetition)

OTHERControl group, CG

The CG groups do not will performed the exercise.

Sponsors

Universidade Federal do Triangulo Mineiro
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
50 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Postmenopausal women (\>12 months amenorrhea) with age above or equal 50 years old. * No hormone therapy or phytoestrogens

Exclusion criteria

* No-drinker alcohol (no alcohol intake whatsoever in their diet); * Non- smokers; * Hypertensive with uncontrolled blood pressure values; * Diabetic with uncontrolled glycemia; * Presence of arthropathies; * Presence of myopathies; * Skeletal musculotendinous disorder.

Design outcomes

Primary

MeasureTime frameDescription
FatigabilityChanges in fatigability measure (e.g. baseline and after 12 weeks of intervention)The fatigability will be evaluate by 60 maximum voluntary isometric contractions (3 s contraction, 2 s rest) in knee extensors at 70 degree.

Secondary

MeasureTime frameDescription
Physical PerformanceChanges in physical performance measure (e.g. baseline and after 12 weeks of intervention)The physical performance will be evaluate by gait speed tests (e.g. 10m walking at usual and fast pace, 400m walk at usual and fast pace).

Other

MeasureTime frameDescription
Body compositionChanges in body composition (e.g. baseline and after 12 weeks of intervention)The body composition will be evaluate by dual-energy X-ray absorptiometry (DXA).
Muscle strengthChanges in muscle strength (e.g. baseline and after 12 weeks of intervention)Muscle strength will be assess in all subjects, by the one-repetition maximum (1-RM) test, for dynamic exercises. The 1-RM is defined as the maximal weight that is lifted with proper body alignment and correct lifting technique.

Countries

Brazil

Contacts

Primary ContactFabio L Orsatti, PhD
fabiorsatti@gmail.com+55343700-6634

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026