Comparing the effect of transcutaneous electrical nerve stimulation and common intervention on the inflammation in people with burn : a randomised control trial study

Phase 3

Conditions: 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

Registration Number: IRCT20240107060644N1

Lead Sponsor: Ahvaz University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 32

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
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.