cesarean section
Conditions
Interventions
The sample will consist of 88 women in the immediate puerperium after cesarean section following the eligibility criteria proposed in the study and distributed according to randomization by Researcher
E02.594.540
E02.331.800
Sponsors
Departamento de Fisioterapia da Universidade Federal do Rio Grande do Norte
Maternidade Divino Amor
Eligibility
Sex/Gender
Female
Inclusion criteria
Inclusion criteria: The volunteers must present between 8 and 12 hours of postpartum cesarean section; having pain on the numerical pain scale = 3 in the region of the cesarean incision7; without clinical or obstetric intercurrences; no infectious process; they should receive the same drug treatment (anti-inflammatory, analgesic and anti-inflammatory drugs) with the same intake interval; postpartum woman with communication and expression difficulties to answer the evaluation questions; not presenting disorders and/or neurological alterations; not presenting musculoskeletal disorders and/or alterations; not being sedentary in the evaluation with the International Physical Activity Questionnaire
Exclusion criteria
Exclusion criteria: Women who give up performing the intervention with Transcutaneous Electrical Nerve Stimulation - TENS; women who give up performing the intervention with the Low Intensity Laser - LBI; volunteers who give up performing the 2 (two) minute walk test during the collection period; volunteers who present clinical and obstetric instability during the collection period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected that the volunteer submitted to the intervention, when compared to the control group, will present better functional performance and alteration in the values ??of the cardio-respiratory physiological variables evaluated through the Global Perception of Change Scale (PGIS) with a score of 7 (much better), Measure of Independence Functional (MIF) with a score of 1 (incomplete independence), 2-minute walk test with increased distance walked, improvement in respiratory rate, Borg scale, heart rate, pulse oximetry and systemic blood pressure. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Public ContactAlane Sena
Departamento de Fisioterapia da Universidade Federal do Rio Grande do Norte
Outcome results
None listed