Delivery by caesarean section, unspecified
Conditions
Interventions
This is a three-arm, single-blind, randomized controlled clinical study of compression taping in immediate postpartum cesarean patients. The number of study arms (groups) described in the report is th
Group TE – receives compression taping combined with therapeutic exercises
Group E – performs only the therapeutic exercises. Each group will have 17 participants, totaling 51 volunteers randomly assigned. The participants will be randomly distributed among the groups throug
Sponsors
Universidade do Estado de Minas Gerais Unidade Divinópolis
Universidade do Estado de Minas Gerais Unidade Divinópolis
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Postpartum women over 18 years of age; who underwent cesarean delivery from 1 to 7 days postpartum; and who did not experience any type of complication during delivery
Exclusion criteria
Exclusion criteria: Women with twin pregnancy; gestational diabetes and preeclampsia; those with complications related to the surgical wound, such as dehiscence and infection; those with hemorrhage, deep vein thrombosis, any other active infections, fever, dehydration, dizziness, and fainting
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| A reduction in abdominal circumference is expected in the group that received early application of compressive taping compared to the control group, after 7 days of intervention;It is expected to find evidence of better healing progress and greater surgical wound comfort in the groups subjected to compressive taping, compared to the group without intervention;Higher patient satisfaction with the applied technique is expected, considering aspects such as perception of relief, comfort, and acceptance of the method ;It is expected to demonstrate that the early use of compressive taping may be a safe and effective intervention in post-cesarean management, contributing to patient well-being and recovery potential | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactJúlia Diniz
Universidade do Estado de Minas Gerais Unidade Divinópolis
Outcome results
None listed