None listed
Conditions
Brief summary
Evaluating the impact of the Smileyscope will assist participating health services in determining the ongoing adoption of the technology for routine clinical use. The evaluation will also inform other Kimberley health services about the impact and acceptability of Smileyscope for Aboriginal children, their families, and their healthcare professionals helping to create regional discussions and approaches to paediatric needle pain and anxiety management.
Interventions
The evaluation of Smileyscope as a pain management strategy for Aboriginal children receiving high volume and regular intramuscular injections will occur through two phases: Phase 1: consented patients will be surveyed about needle pain and anxiety in a usual care setting (monthly for a period of three months) Phase 2: consented patients will be offered the opportunity to use Smileyscope; a virtual reality headset, designed specifically for children's needle anxiety and pain management. Virtual reality digital content is played through a smartphone via software application. The smartphone is placed into the a Google Daydream headset which provides a stereoscopic display to create a 3D experience. The virtual reality experience will be provided as an adjunct to standard care (e.g. topical local anaesthetic) during the needle procedure. The content is an animated and immersive age-appropriate visualisation. The intervention will be delivered by the proceduralists (doctors, nurses, Aboriginal Health Workers). The intervention (Smileyscope) will take place for 10 minutes, per monthly visit, for 3 months. Consented patients will continue to be surveyed about needle pain and anxiety (monthly for a period of 3 months). During Phase 2 families of consented patients and healthcare professionals involved in the administration of the needle will be offered qualitative interviews to discuss process, impacts and acceptability of Smileyscope as a needle pain/anxiety management strategy. NB: Participants in Phase 1 and Phase 2 will be the same cohort.
Sponsors
Study design
Eligibility
Inclusion criteria
Primary sample 1.Children between the age of 4 to 16 years inclusive who have been prescribed large volume and regular intramuscular injections (i.e LA Bicillin injections for children with history of Acute Rheumatic Fever or Rheumatic Heart Disease). Secondary Samples 2. Parents of eligible children 3. Healthcare professionals of eligible children Responses below relate to primary sample.
Exclusion criteria
1. Children who are significantly unwell or clinically deteriorating as judged by the treating clinical team 2. Inability to complete consent or study instruments