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At their fingertips: The effects of child-led distraction using a tablet computer on children’s distress and pain during painful medical procedures; a randomised controlled trial.

At their fingertips: The effects of child-led distraction using a tablet computer on children’s distress and pain during painful medical procedures; a randomised controlled trial.

Status
Terminated
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617001570370
Enrollment
49
Registered
2017-11-22
Start date
2017-10-30
Completion date
2018-03-14
Last updated
2018-08-20

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

Conditions

None listed

Brief summary

Managing pain and distress for hospitalised children undergoing medical procedures is very important as it reduces the occurrence of paediatric medical traumatic stress and other significant negative outcomes (Lindeke et al., 2006). Evidence has shown that non-pharmacological interventions such as distraction are a highly successful method in reducing distress and pain in adult and paediatric patients. At present, paediatric patients undergoing painful procedures do not routinely receive distraction therapy due to limitations such as time. With modern technology rapidly evolving, research designed to assess the effectiveness of child-led distraction using a tablet computer in reducing distress and pain in children undergoing painful medical procedures is essential. Through exploring this, a valuable contribution may promote the therapeutic practice and improve health care outcomes for children and their families. The results of this study will assist in determining whether child-led distraction through the use of a tablet computer (Apple iPad) reduces distress, pain and procedural time by incorporating a wide range of distraction methods in one convenient and cost-effective device.

Interventions

This study will be conducted in a Western Australian tertiary paediatric hospital within the Ambulatory Care Day-stay Facility (ACDF) by a Registered Nurse/Researcher. A randomised controlled trial with one control group and one experimental group will be undertaken. The experimental group will receive ‘standard care’ from their parents and healthcare professionals and the distraction of the tablet computer (Apple iPad) to self-lead their own distraction. The tablet computer will be offered to t

This study will be conducted in a Western Australian tertiary paediatric hospital within the Ambulatory Care Day-stay Facility (ACDF) by a Registered Nurse/Researcher. A randomised controlled trial with one control group and one experimental group will be undertaken. The experimental group will receive ‘standard care’ from their parents and healthcare professionals and the distraction of the tablet computer (Apple iPad) to self-lead their own distraction. The tablet computer will be offered to the child upon entering the treatment room in view of the intravenous cannulation procedure. The tablet computer will be provided 5 minutes prior to the commencement of the procedure to allow the child time to familiarise themselves with the tablet computer and decide on a distraction. The tablet will be returned on completion of the procedure. A wide number of age-specific applications will be uploaded onto the tablet computer with audio, visual, audio-visual and virtual reality applications from which to choose. Time spent engaging with the iPad will be collected over four time points including prior to insertion of needle (from the time the nurse enters the room to the time the needle is inserted); during the needle insertion (whilst the needle is being inserted to the time the needle has been placed in a vein and deemed complete); after the needle is inserted (From the time the needle is placed into the vein until the dressings have been applied and the procedure is deemed complete) and total time spent engaging with the iPad. This will be collected by the researcher and will allow the assessment of intervention adherence/fidelity. Parents/guardians are permitted and encouraged to engage with the tablet computer with their child. The control group will receive ‘standard care’ from their parents and health professionals. Standard care is described as standard treatment during medical procedures including local anaesthetic cream (EMLA), parental and professional reassurance, encouragement, involvement and comforting. Stratified randomisation will be used to allocate the children to the control or intervention group by a computer generated program to ensure that equal numbers of participants of similar ages are allocated to each group.

Sponsors

Princess Margaret Hospital for Children
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Months to 12 Years
Healthy volunteers
No

Inclusion criteria

Participants will be young children aged between 18 months up 12 years of age requiring intravenous cannulation for a procedure/treatment prior scheduled. -Developmentally appropriate to lead the distraction; and - must have participant assent where suitable and parental/guardian consent. - All children must have topical anaesthetic cream (EMLA) applied for 60 minutes prior to the procedure.

Exclusion criteria

- Children who require or have received sedation; - Children who have taken steroids or ADHD medications within the last month; - Children where response to painful stimuli maybe altered by neuromuscular disease (e.g.: Cerebral palsy); - Children without topical anaesthetic cream; - Non-English speaking children and/or parents/guardians; and - Children who have been diagnosed with anxiety or ADHD.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026