Virtual reality-based distraction for intravenous insertion-related distress in children: a study protocol for a randomised controlled trial

被引:4
作者
Ali, Samina [1 ]
Rajagopal, Manasi [1 ]
Stinson, Jennifer [2 ,3 ]
Ma, Keon [4 ]
Vandermeer, Ben [5 ]
Felkar, Bailey [6 ]
Schreiner, Kurt [7 ]
Proctor, Amanda [8 ]
Plume, Jennifer [9 ]
Hartling, Lisa [1 ,5 ]
机构
[1] Univ Alberta, Fac Med & Dent, Pediat, Edmonton, AB, Canada
[2] Univ Toronto, Hosp Sick Children, Child Hlth Evaluat Sci, Res Inst, Toronto, ON, Canada
[3] Univ Toronto, Lawrence S Bloomberg Fac Nursing, Toronto, ON, Canada
[4] Univ Calgary, Pediat, Cumming Sch Med, Calgary, AB, Canada
[5] Univ Alberta, Alberta Res Ctr Hlth Evidence, Pediat, Edmonton, AB, Canada
[6] London Hlth Sci Ctr Childrens Hosp, London, ON, Canada
[7] Univ Alberta, Pediat, Pediat Parents Advisory Grp, Edmonton, AB, Canada
[8] Alberta Hlth Serv, Stollery Youth Advisory Council & Patient & Famil, Edmonton, AB, Canada
[9] Stollery Childrens Hosp, Alberta Hlth Serv, Edmonton, AB, Canada
来源
BMJ OPEN | 2022年 / 12卷 / 03期
关键词
PEDIATRIC EMERGENCY-DEPARTMENT; NUMERICAL RATING-SCALE; PAIN INTENSITY; PROCEDURAL PAIN; AUDIOVISUAL DISTRACTION; EXPOSURE THERAPY; SELF-REPORT; INTERVENTION; ANXIETY; MUSIC;
D O I
10.1136/bmjopen-2021-057892
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Intravenous (IV) insertions are among the most performed procedures for children seeking medical care; they are often a painful and stressful experience for both children and their caregivers. Paediatric distress and pain that is inadequately treated may lead to a frightened and uncooperative child, repeated IV attempts and overall frustration with care for both the family and clinical team. We hypothesise that distraction via an immersive virtual reality (VR) experience may reduce the associated distress for children undergoing IV insertions. Methods and analysis This two-armed randomised controlled superiority trial will be conducted in a Canadian paediatric emergency department and will aim to enrol 80 children overall. Children will be randomised to receive either departmental standard of care alone or standard of care plus an immersive VR experience. Children 6-17 years of age who are undergoing IV insertion and have topical anaesthetic application will be considered for inclusion. Our primary objective is to compare the reduction of distress between the two study arms. The primary outcome will be the child's observed distress score as measured by the Observational Signs of Behavioral Distress-Revised tool. Secondary outcomes include the child's pain intensity and fear, parental anxiety, satisfaction with the IV procedure, as well as adverse events. Recruitment launched in September 2020 and is expected to end in March 2022. Ethics and dissemination This study has been approved by the Health Research Ethics Board (University of Alberta). Informed consent will be obtained from parents or guardians, and assent from children. Study data will be submitted for publication irrespective of results. This study is funded through a Women and Children's Health Research Institute Innovation grant. Purchase of the VR equipment was facilitated through a Stollery Children's Hospital Foundation small equipment grant.
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页数:9
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