Condition 1: Thermal burn. Condition 2: Thermal burn. Condition 3: Thermal burn. Condition 4: burn disease. Burn and corrosion of shoulder and upper limb, except wrist and hand Burn and corrosion of wrist and hand Burn and corrosion of lower limb, except ankle and foot Burn and corrosion of ankle and foot
Conditions
Interventions
Intervention 1: Intervention group: In addition to conventional treatment, participants in this group also receive electrical stimulation, which involves applying electrical stimulation to the skin ne
Sponsors
Ahvaz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: People between 18 and 60 years old The occurrence of burns in the first 24 hours People with second and third degree burns with a burn level of less than 50% Alert people with the ability to respond
Exclusion criteria
Exclusion criteria: People with inhalation burns Patients on mechanical ventilation Pregnant women People with psychiatric problems People with psychiatric problems, pre-existing liver disease such as liver cirrhosis or hepatitis History of inflammatory diseases such as osteoarthritis and inflammatory bowel disease, or conditions that they affect the amount of CRP and Albumin, such as acute pancreatitis, myocardial infarction, acute infection, malnutrition and nephrosis, burns with trauma or organ failure, unwillingness of the individual to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| C-reactive protein. Timepoint: Before the intervention and 24 and 48 hours after the end of the intervention. Method of measurement: Cell counter.;Albumin. Timepoint: Before the intervention and 24 and 48 hours after the end of the intervention. Method of measurement: Cell counter.;Pain. Timepoint: Before the intervention and 24 and 48 hours after the end of the intervention. Method of measurement: Visual Analogue Scale. | — |
Secondary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Before the intervention and 48 and 72 hours after the intervention. Method of measurement: Chen et al.'s sleep quality questionnaire.;Pain-related feelings and thoughts score. Timepoint: Before the intervention and 48 and 72 hours after the intervention. Method of measurement: Pain catastrophizing questionnaire.;Fear of movement score. Timepoint: Before the intervention and 48 and 72 hours after the intervention. Method of measurement: Tampa Scale Kinesiophobia questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNeda Orakifar
Ahvaz University of Medical Sciences
Outcome results
None listed