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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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201605016834N9
Enrollment
60
Registered
2016-07-11
Start date
2016-07-05
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Second-degree burn patients. Burns and corrosions of external body surface, specified by site

Interventions

Intervention 1: In virtual reality group: playing images and sounds of a waterfall with a virtual reality head set, once a session on 5 consecutive days during dressing (the third to seventh day burni
In virtual reality group: playing images and sounds of a waterfall with a virtual reality head set, once a session on 5 consecutive days during dressing (the third to seventh day burning) will be perf
In multimedia system group: playing images and sounds of a waterfall with a LCD devices, once a session on 5 consecutive days during dressing (the third to seventh day burning) will be performed. Befo
For the control group during the intervention is intended for routine care.

Sponsors

Research Vice- Chancellor, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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).

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026