Pathological Conditions
Conditions
Interventions
The intervention will take place in 30 volunteers in each group.
The 1st stage performed before the oculomotor maneuver was performed, with the patient at rest for 10 minutes without team intervention
Other
E02.779
Sponsors
Universidade Federal do Piauí
Universidade Federal do Piauí
Eligibility
Age
18 Years to 30 Years
Inclusion criteria
Inclusion criteria: The participants were healthy; aged between 18 and 30 years old; regardless of gender; who agreed to conduct the research by signing the informed consent form (ICF).
Exclusion criteria
Exclusion criteria: The individuals who reported psychiatric problems; neurological diseases; glaucoma; constant use of drugs; women in menstrual periods or pregnant women and people who were using contact lenses did not participate in the research; in addition to those who requested to withdraw from the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that there will be a 20% reduction in blood pressure, heart and respiratory rate, and an improvement in oxygen saturation, verified by the sphygmomanometer and oximeter, respectively, from the observation of a variation of at least 5% in the measurements. pre and post intervention (intragroup and intergroup) | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactGuilherme de Morais Gouveia
Universidade Federal do Piauí
Outcome results
None listed