Coronary disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Men with a diagnosis of ischemic coronary disease; above 45 years of age; who do not present a history of smoking or alcoholism; cardiovascular rehabilitation program followers who do not present a historical recruitment period for infections; do not present with unstable angina; controlled hypertension; without significant valvular disease; without uncontrolled metabolic disease
Exclusion criteria
Exclusion criteria: Volunteers will be excluded from the study when time series records of RR intervals show less than 95% of sinus beats; absence of attendance in at least one of the stages of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Outcome expected 1 The autonomic behavior will be evaluated by analyzing the heart rate variability determined at the beginning and end of the care. An increase in the measures of heart rate variability is expected for the indices that evaluate the parasympathetic autonomic behavior (RMSSD, HF, SD1), immediately after the intervention protocol. | — |
Secondary
| Measure | Time frame |
|---|---|
| Outcome expected 2 Cutaneous temperature through the thermographic camera The outcome will be assessed pre and post intervention. Reduction of cutaneous temperature is expected immediately after the intervention protocol is performed.;Outcome expected 3 Blood pressure through the sphygmomanometer and stethoscope The outcome will be assessed pre and post intervention. Reduction of blood pressure is expected immediately after the intervention protocol is performed.;Outcome expected 4 Heart rate through the heart monitor. The outcome will be assessed pre and post intervention. Reduction of heart rate is expected immediately after the intervention protocol is performed. | — |
Countries
Brazil
Contacts
Núcleo de Pesquisa do Instituto Docusse de Osteopatia e Terapia Manual