Comparison of efficacy of two methods of virtual reality and multimedia system on pain and pain anxiety in burn patient during dressing change: A randomized controlled clinical trial
Not Applicable
- Conditions
- Second-degree burn patients.Burns and corrosions of external body surface, specified by siteT20, T25
- Registration Number
- IRCT201605016834N9
- Lead Sponsor
- Research Vice- Chancellor, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
patients who are hospitalized in the burn ward of arrival; have not the history of previous burns; are in burns below 25% and second- degree; are acute phase of burn (48 to 72 hours after burn); are 18 years and older; are interested in participating in the study; are conscious and orientated; have not sight and hearing problems; are not addicted; had general health over the past month; absence of numbness in the limbs target; are not diabetic(due to lack of feeling pain). Exclusion criteria: patients who not want to continue the cooperation in the study; are transferred to another ward; have absence more than one meeting; taking pain killers or sedative without prescription; taking skin graft.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Before the intervention, immediately after intervention 5 consecutive days (the third to seventh day burning). Method of measurement: Visual Analogue Scale (VAS): 0–10 Numeric Pain Rating Scale.
- Secondary Outcome Measures
Name Time Method Pain anxiety. Timepoint: Before the intervention, immediately after intervention 5 consecutive days (the third to seventh day burning). Method of measurement: Burn Specific Pain Anxiety Scale (BSPAS).