Condition 1: Burn of second degree of trunk. Condition 2: Burn of second degree of shoulder and upper limb, except wrist and hand. Condition 3: Burn of second degree of wrist and hand. Condition 4: Burn of second degree of lower limb, except ankle and foot. Condition 5: Burn of second degree of ankle and foot. Burn of second degree of trunk Burn of second degree of shoulder and upper limb, except wrist and hand Burn of second degree of wrist and hand Burn of second degree of lower limb, exce
Conditions
Interventions
Intervention 1: Control group: This group includes people who have had second-degree burns and change their dressings daily at the specified hour, and their anxiety level for half an hour before going
Sponsors
Oroumia University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: People between the ages of 18-60. Emergency stage (72-48 hours after burn injury until complete wound closure) have been passed and the patients have been in the subsequent stages of burn injury (acute and rehabilitation). Patients with secondary degree burns with a burn level between 9-35%. No burns in the neck and face. Ability to speak Persian Do not have severe hearing or visual impairment Willing to participate in the study. The patient does not have a history of mental illness The patient does not have a history of burns.
Exclusion criteria
Exclusion criteria: The patient dose have burns in the neck and face area The patient dose have severe hearing or visual impairment The patient does have a history of mental illness The patient does have a history of burns.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The patients' baseline pain intensity was measured at session zero before dressing replacement and then measured in four consecutive steps daily before and after dressing. Timepoint: Meeting0, meeting1(day1), meeting2(day2), meeting3(day3), meeting4(day4). Method of measurement: The Short Form of Mc Gill Pain Questionnaire.;The patients' baseline pain quality was measured at session zero before dressing replacement and then measured in four consecutive steps daily before and after dressing. Timepoint: Meeting0, meeting1(day1), meeting2(day2), meeting3(day3), meeting4(day4). Method of measurement: Visual Analogue Scale (VAS).;The patients' baseline pain anxiety was measured at session zero before dressing replacement and then measured in four consecutive steps daily before dressing. Timepoint: Meeting0, meeting1(day1), meeting2(day2), meeting3(day3), meeting4(day4). Method of measurement: The abbreviated burn specific pain anxiety scale. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactNader Aghakhani
Oroumia University of Medical Sciences
Outcome results
None listed