Wound
Conditions
Interventions
This is a three-arm, double-blind, randomized controlled trial. A total of 159 people who meet the eligibility criteria will be allocated probabilistically to one or other intervention group using a r
E05.599.395.642.550
Sponsors
Universidade do Estado da Bahia
Secretaria Municipal de Saúde de Salvador
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Being 18 years of age or older; both genders; have a wound that has existed for four weeks or more, and complain of moderate to severe pain
Exclusion criteria
Exclusion criteria: Patients with altered hearing acuity; patients with disorientation in time and space
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In the intervention with hypnosis, it is expected to find a reduction in at least 2 levels of pain initially measured with patients with chronic wounds after applying the dressing when compared to patients in the control group | — |
Secondary
| Measure | Time frame |
|---|---|
| In the intervention groups with hypnosis and hypnosis with Neurolinguistic Programming, it is expected to find a reduction in the level of pain when compared to the control group;In the hypnosis intervention group, it is expected to find a difference in the reduction of pain levels when compared to the hypnosis intervention group with neurolinguistic programming. | — |
Countries
Brazil
Contacts
Public ContactMagno das Mercês
Universidade do Estado da Bahia
Outcome results
None listed