Impact of Guided Imagery Implementation on the Quality and Severity of Pain, and Pain Anxiety of Change Dressing in Patients with Burn Injury

Not Applicable

Completed

• Conditions: 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, except ankle and foot; Burn of second degree of ankle and foot; T21.2; T22.2; T23.2; T24.2

• Registration Number: IRCT20180813040786N1
• Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 21 April 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 56

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

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.

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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.