Anxiety
Conditions
Interventions
Experimental group (n=100): Participants will be submitted to musical hearing in the immediate preoperative period (up to 24 hours before surgery) and on the first postoperative day (24 to 48 hours af
Behavioural
E02.190
Sponsors
Universidade Federal do Triângulo Mineiro
Universidade Federal do Triângulo Mineiro
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients undergoing elective cardiac surgery by median longitudinal sternotomy during the data collection period.
Exclusion criteria
Exclusion criteria: Patients who are unable to maintain dialogue with the researcher; who have deficit or hearing and / or cognitive impairment; who are using sedative or anxiolytic medications.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction in state anxiety scores, assessed in the immediate preoperative period, checked by applying the Inventory of State-Trait Anxiety (STAI), based on the finding of a variation of at least 1% in pre and post intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Reduction of pain intensity scores in the immediate postoperative period, measured by the Numerical Pain Scale, based on the finding of a variation of at least 1% in pre and post intervention measurements. ;Blood pressure reduction in the immediate postoperative period, verified by auscultatory measurement, using a stethoscope and calibrated adult aneroid sphygmomanometer, based on the finding of a variation of at least 1% in pre and post intervention measurements.;Heart rate reduction in the immediate postoperative period, verified by portable pulse oximeter measurement, based on the finding of at least 1% variation in pre- and post-intervention measurements.;Increased oxygen saturation in the immediate postoperative period, verified by measuring with portable pulse oximeter, based on the finding of a variation of at least 1% in pre and post-intervention measurements.;Reduction of respiratory rate in the immediate postoperative period, verified by observing and counting the respiratory movements for one minute, based on the finding of a variation of at least 1% in pre and post-intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactMaria Helena Barbosa
Universidade Federal do Triângulo Mineiro
Outcome results
None listed