Breast neoplasms
Conditions
Interventions
Unblinded randomized clinical study. 51 women will be allocated to the experimental group and 51 to the control group, totaling 102 women. Participants will be randomized to the experimental group (G1
the ten envelopes will contain a code that will allocate five participants to the intervention group (G1) and five to the control group (G2). Randomization will then be carried out through a simple dr
E07.101.036
Sponsors
Hospital de Clínicas de Porto Alegre
Universidade Federal do Rio Grande do Sul
Eligibility
Sex/Gender
Female
Age
20 Years to 70 Years
Inclusion criteria
Inclusion criteria: be female; be between 20 and 70 years of age; having been diagnosed with breast cancer; have indication for surgical treatment of oncoplastic or breast reconstructive surgery.
Exclusion criteria
Exclusion criteria: have an allergy to the taping tape; present psychological or cognitive disorders that prevent understanding of the research and assessment instruments; participants who develop infections, hemorrhages, bruises or other complications in the P.O. will be excluded from the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Measurement of edema approximately seven days after taping application through self-perception using a visual analogue scale and photographic evaluation; measurement of bruising approximately seven days after taping application through photographic assessment; pain measurement approximately seven days after taping application through self-perception using a visual analogue scale; measuring the participants' physical well-being approximately seven days after taping application using the BREAST-Q questionnaire. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected. | — |
Countries
Brazil
Contacts
Public ContactAndressa da Rosa
Universidade Federal do Rio Grande do Sul
Outcome results
None listed