The Effect of Therapeutic Play on Pain, Fear and Emotional Indicator
The Effect of Therapeutic Gaming Used in Preparation for Hydrothera-py Treatment on Children's Pain, Fear and Emotional Indicators: A Ran-domized, Controlled, Treatment Study
1 other identifier
interventional
64
1 country
1
Brief Summary
This study was planned to determine the effect of therapeutic play and preparation for hydrotherapy treatment on pain, fear and emotional indicator levels in children with burn injuries. It is an experimental randomized controlled study. The population of the research will be children between the ages of 3-6 who are hospitalized in the Pediatric Burn Intensive Care Unit. As a result of the power analysis using the G\*Power 3.0.10 program, at least 52 children in total (control group 26, therapeutic play group 26) with 50% power, 0.05 alpha margin of error, 0.80 beta margin of error and 20% effect size. was determined to be included in the study. However, considering the case losses, the number of children to be included in the study was determined as 64 by increasing the sample size by 20%. The data will be collected between the dates to be determined by the researcher after obtaining the ethics committee approval and written permission from the institution where the research will be conducted. Introductory information form, FLACC Pain Scale, Child Fear Scale and Child Emotional Indicators Scale will be used to collect research data. The research will be conducted with the children of parents who agreed to participate in the study. There are two groups, the control group and the experimental group. While the routine practice of the clinic will be applied to the control group, creative therapeutic games will be played to the experimental group together with the routine practice. Children will be stratified according to their pain scores, fear scores and burn depth (degree) and will be assigned to an equal number of children in each group using the blocking method. Before the procedure, the introductory information form will be filled in by the researcher in line with the patient file and parent information. After parents are informed about which group the child is in, their written consent will be obtained.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Jan 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 8, 2023
CompletedFirst Posted
Study publicly available on registry
April 11, 2023
CompletedStudy Start
First participant enrolled
January 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2025
CompletedDecember 12, 2023
December 1, 2023
1 year
January 8, 2023
December 5, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
The change in the pain level of the children will be evaluated by applying the FLACC pain scale to the children by the researcher.
therapeutic game was played for children 10 minutes before hydrotherapy treatment
Pain assessment will be done 30 minutes before hydrotherapy treatment.
The change in the pain level of the children will be evaluated by applying the FLACC pain scale to the children by the researcher.
therapeutic game was played for children 10 minutes before hydrotherapy treatment
Pain assessment will be done 10 minutes after hydrotherapy treatment.
The change in the pain level of the children will be evaluated by applying the FLACC pain scale to the children by the researcher.
therapeutic game was played for children 10 minutes before hydrotherapy treatment
Pain assessment will be done 30 minutes after hydrotherapy treatment.
Secondary Outcomes (3)
The change in the children's fear level will be evaluated by applying the Child Fear Scale to the children by the researcher.
Fear assessment will be done 30 minutes before hydrotherapy treatment.
The change in the children's fear level will be evaluated by applying the Child Fear Scale to the children by the researcher.
Fear assessment will be done 10 minutes after hydrotherapy treatment.
The change in the children's fear level will be evaluated by applying the Child Fear Scale to the children by the researcher.
Fear assessment will be done 30 minutes after hydrotherapy treatment.
Other Outcomes (1)
The change in children's emotional status will be evaluated by applying the Children's Emotional Indicators Scale to the children by the researcher.
Emotional indicators will be evaluated at the 10th minute of hydrotherapy treatment.
Study Arms (2)
therapeutic game group
ACTIVE COMPARATORtherapeutic play will be played 10 minutes before the hydrotherapy treatment.
control group
NO INTERVENTIONNo intervention was given to the children prior to hydrotherapy treatment.
Interventions
therapeutic game will be played to prepare children for hydrotherapy treatment
Eligibility Criteria
You may qualify if:
- The child is between 3-6 years old
- The child is receiving the first hydrotherapy treatment in the clinic.
- Presence of second and/or third degree superficial and/or deep burns
- Volunteering of the child and family to participate in the research
- The child was given analgesics half an hour before the procedure.
- No simultaneous debridement during hydrotherapy
- Burn width between 20%-70%
You may not qualify if:
- The child is younger than 3 years old, over 6 years old
- Presence of any other chronic disease other than burns
- The child is receiving mechanical ventilator support.
- Having a trecheostomy done to the child
- The child has been given sedative medication in the last 8 hours.
- Having a companion other than mother or father
- Hydrotherapy treatment takes less than 30 minutes, more than 45 minutes
- The child does not want to play
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Eskisehir Osmangazi University
Eskişehir, Odunpazarı, 26000, Turkey (Türkiye)
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- FACTORIAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Nurse
Study Record Dates
First Submitted
January 8, 2023
First Posted
April 11, 2023
Study Start
January 1, 2024
Primary Completion
January 1, 2025
Study Completion
January 1, 2025
Last Updated
December 12, 2023
Record last verified: 2023-12
Data Sharing
- IPD Sharing
- Will not share