Healthy Volunteers
Conditions
Interventions
This study employs a randomized, single-blind and parallel design. Participants will undergo four trials (2 × familiarization, 1 × baseline, and 1 × experimental) to evaluate the maximum number of rep
http://www.gpower.hhu.de) employing a three-group, repeated measures design with a moderate effect size (f = 0.6), a = 0.05, power (1-ß) = 0.8, and a correlation of 0.5, indicated a minimum sample siz
D26.660
Sponsors
Instituto de Ciências Biológicas da Universidade Federal de Juiz de Fora
Instituto de Ciências Biológicas da Universidade Federal de Juiz de Fora
Eligibility
Sex/Gender
Male
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: Healthy subjects; Age between 18 and 40 years old; male; experience with resistance exercise of at least one year
Exclusion criteria
Exclusion criteria: Smoking history; presence of any metabolic or cardiovascular disease; arterial hypertension (=140/90 mmHg or use of antihypertensive medications); use of anabolic steroids, drugs or medications with potential impact on physical performance; recent musculoskeletal injury; previous experience with pneumatic occlusion intervention
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Expected outcome 1 Number of repetitions;Outcome found 1 Number of repetitions;Expected outcome 2 Maximal voluntary isometric contraction;Outcome found 2 Maximal voluntary isometric contraction;Expected outcome 3 Power output;Outcome found 3 Power output | — |
Secondary
| Measure | Time frame |
|---|---|
| Expected outcome 4 Surface electromyography;Outcome found 4 Surface electromyography;Expected outcome 5 Rating of perceived exertion;Outcome found 5 Rating of perceived exertion;Expected outcome 6 Expectation;Outcome found 6 Expectation;Expected outcome 7 Belief;Outcome found 7 Belief | — |
Countries
Brazil
Contacts
Public ContactHiago Souza
Universidade Federal de Juiz de Fora
Outcome results
None listed