Effects of the application of Therapeutic Ultrasound associated with Eletrical Stimulation in Pain and Funcionality in women cesarian sectio
- Conditions
- Cesarean SectionPainC23.888.592.612E04.520.252.500
- Registration Number
- RBR-6wq24d
- Lead Sponsor
- niversidade Federal Do Paraná
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruitment completed
- Sex
- Female
- Target Recruitment
- Not specified
Women over 15 years of age;underwent cesarean during labor for at least 8 hours and a maximum of 24 hours after the procedure; post-cesarean pain
illiterate or non-oriented; presence of puerperal intercurrences such as: local bleeding requiring intervention, signs suggestive of infection, fever, anesthetic complications and breast intercurrences; diagnosis of epilepsy, demyelinating disease, spindle trauma, tumors, diabetes mellitus and hypertension; puerperal women who use pacemakers or implanted electronic devices; presence of local drainage system and; irritation or intolerance to the application of Combination Therapy (history of allergy or intolerance to the application of electrical current or therapeutic ultrasound)
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The post-cesarean political situation during the immediate puerperium, controlled by the McGill questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements;A post-cesarean functional limitation during the immediate puerperium, selected by the Functional Capacity Check, based on the observation of a variation of at least 5% in the pre and post-intervention measurements
- Secondary Outcome Measures
Name Time Method The painful condition during the immediate puerperium, verified by the McGill questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements in the period of 7 days;The functional limitation after cesarean section during the immediate puerperium, verified by the Functional Capacity Verification questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements in the period of 7 days