Efficacy of Animation, Buzzy, and Multiple Interventions on Pain in Children: A Randomised Controlled Trial

Sponsor

Karadeniz Technical University (Other)

Overall Status

Completed

CT.gov ID

NCT05374902

Collaborator

(none)

180

Enrollment

Locations

Arms

1.4

Actual Duration (Months)

Patients Per Site

41.5

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of the study was to determine the effects of providing procedural informational animation, Buzzy application during the procedure, the combination of both interventions (Animated video and Buzzy), and standard care on pain management during venipuncture in children aged 6-12 years.

Condition or Disease	Intervention/Treatment	Phase
Pain, Procedural Child Phlebotomy Venipuncture	Other: Providing procedural informational animation video Device: Buzzy Combination Product: Multiple interventions	N/A

Detailed Description

A prospective randomized controlled trial design was used to determine the effects of Buzzy, procedural informational animation, multiple interventions (Buzzy and Animated video), and standard care on the pain level of 6-12 years aged children during venıpunctrue. The study was conducted in the territory hospital pediatric blood collection unit The sample size was determined by power analysis and 45 child-parent pairs were included in each group. The patients who met the sample selection criteria were randomly and equally assigned into 4 groups using a computer-based program. As a data collection tools, Data Collection Form and Wong-Baker have been used. Venipuncture-related pain was self-reported by each child, as well as through parents and nurse. Children in the multiple interventions group were shown procedural informative animation and the venipunctıre procedure was performed with buzzy®. Standard care was applied to the control group, in which no local anesthetic was used and families could accompany the bloodletting process. The pain responses of the children were evaluated twice, immediately after the procedure (while the child was sitting in the blood collection chair) and 2-3 minutes after the procedure, both by the children's self-reports and by the parents and the nurse.

Study Design

Study Type:

Interventional

Actual Enrollment :

180 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Masking Description:

Single (investigator)

Primary Purpose:

Supportive Care

Official Title:

Efficacy of Procedural Information, Buzzy, and Multiple Interventions on Pain Management in Undergoing Venipuncture Children: A Randomised Controlled Trial

Actual Study Start Date :

Sep 1, 2021

Actual Primary Completion Date :

Oct 15, 2021

Actual Study Completion Date :

Oct 15, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Procedural informational animation group Children and parents have watched procedural informational animation before venipuncture. Afterward, the children and their parents entered the blood drawn unit, and the procedure was performed as in standard care.	Other: Providing procedural informational animation video Children and parents have watched procedural informational animation before venipuncture. Afterward, the children and their parents entered the blood drawn unit, and the procedure was performed as in standard care.
Experimental: Buzzy group Buzzy® was placed on the injection site and cold application and vibration were turned on 60 s before the procedure. Then, the nurse moved Buzzy® about 3-5 cm above the injection site. The procedure was performed with buzzy®. The Buzzy® intervention and phlebotomy were terminated at the same time.	Device: Buzzy Buzzy® was placed on the injection site and it was turned on 60 s before the procedure. Then, the nurse moved Buzzy® about 3-5 cm above the injection site. The procedure was performed with buzzy®. The Buzzy® intervention and phlebotomy were terminated at the same time.
Experimental: Multiple interventions group Children and parents have watched procedural informational animation before venipuncture. Afterward, the children and their parents entered the blood drawn unit. Buzzy® was placed on the injection site and cold application and vibration were turned on 60 s before the procedure. Then, the nurse moved Buzzy® about 3-5 cm above the injection site. The procedure was performed with buzzy®. The Buzzy® intervention and phlebotomy were terminated at the same time.	Combination Product: Multiple interventions Watching procedural informational animation video prior to venipuncture, and Buzzy application during venipuncture
No Intervention: Control group Children in this group received standard care. A local anesthetic is not used, and the parents are with their children during the procedure in the standard care of the blood collection unit

Outcome Measures

Primary Outcome Measures

Pain assessment [The pain was measured at 30 seconds after (immediately) the venipuncture.]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."
Pain assessment [The pain was measured at 2-3 minutes after the venipuncture.]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."

Secondary Outcome Measures

Pain assessment - parent [The pain was measured at 30 seconds after (immediately) the venipuncture by parent]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."
Pain assessment - parent [The pain was measured at 2-3 minutes after the venipuncture by parent]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."
Pain assessment - nurse [The pain was measured at 30 seconds after (immediately) the venipuncture by nurse.]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."
Pain assessment - nurse [The pain was measured at 2-3 minutes after the venipuncture by nurse.]
Pain intensity was assessed Wong-Baker FACES Pain Rating Scale. It is used to determine the pain level of children aged between 3 and 18 years through their facial expressions which are assigned the values of 0 and 10. The first face represents a pain score of 0, and indicates "no hurt". The last face represents a pain score of 10, and indicates "hurts worst."

Eligibility Criteria

Criteria

Ages Eligible for Study:

6 Years to 12 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Inclusion Criteria:

being between the ages of 6 and 12 years,
admitted to the hospital as an outpatient,
having complete skin integrity at the place where the Buzzy device will be inserted
having the ability to verbally communicate
parents being literate.

Exclusion Criteria:

having any acute pain at the time of the procedure
having any audiovisual, cognitive sensitivity, or physical disability and having a chronic or life-threatening disease
being under the influence of any sedative/anticonvulsant/analgesic drug,
getting blood drawn in the last month
failure to phlebotomy at the first attempt
having nerve damage or peripheral neuropathy.