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The Effect of Sticker Intervention on Pain and Anxiety

The Effect of Sticker Intervention on Pain and Anxiety Experienced During IV Intervention

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07245043
Enrollment
72
Registered
2025-11-24
Start date
2025-07-01
Completion date
2025-10-24
Last updated
2025-11-24

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

Conditions

Anxiety, INTRAVENOUS CATHETER APPLICATION, Pain, Pain Management

Keywords

intravenous catheter application, children, pain management, anxiety

Brief summary

Peripheral venous catheterization, which involves the placement of an invasive device into the lumen of a peripheral vein, is a commonly used procedure in children receiving hospital treatment.IV insertion is a particularly painful and stressful experience for children. This is because children have more limited coping skills than adults. This study was designed as a randomized controlled trial to examine the effect of sticker intervention on pain and anxiety experienced during IV insertion.

Detailed description

The study consists of an sticker group and a control group. Participants will be assigned to groups using stratified randomization. Anxiety levels in both groups will be assessed using the Children's Anxiety Scale-State (ÇAS-D), while pain levels will be evaluated by both the child and the researcher using a visual pain scale before, during, and after the procedure.For children in both groups, 10 minutes before the intravenous procedure, both the child and the researcher will rate the child's anxiety and pain using scales.During the IV procedure, the researcher will place the sticker chosen by the child on the IV insertion site. Meanwhile, the researcher will rate the child's anxiety and pain using scales. No sticker will be placed on the IV insertion site of the control group, and the child's anxiety and pain will be rated using scales.For both groups, 10 minutes after the intravenous procedure, both the child and the researcher will rate the child's anxiety and pain using scales.

Interventions

BEHAVIORALcontrol group

Children in the control group will not undergo any procedures other than routine hospital procedures. Children's anxiety and pain will be assessed based on both the researcher's and the child's reports before, during, and after the procedure, following consent from the mothers.

Sponsors

Harran University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Before implementing data collection tools, children and mothers will be informed, and data will be collected through face-to-face interviews using data collection forms after obtaining consent from those who agree to participate in the study. Children in the sticker group will be provided with stickers by the researcher during the application phase, which they can choose according to their own preferences.Children's anxiety and pain will be assessed based on both the researcher's and the child's reports before, during, and after the procedure, following consent from the mothers.

Eligibility

Sex/Gender
ALL
Age
5 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

* Children aged 5-10 years, * Children undergoing painful procedures * Children undergoing IV procedures

Exclusion criteria

* Children who have undergone surgery, * Children who have undergone procedures other than intravenous interventions, * Children whose parents are not present, * Children with any chronic illness or additional complaints that may trigger pain from the procedure, * Children with mental retardation

Design outcomes

Primary

MeasureTime frameDescription
1. Outcome MeasuresFor children in both groups: Ten minutes before the intravenous procedure, during the procedure, and ten minutes after the procedure, both the child and the researcher will rate the child's anxiety and pain using scales.The outcome measures for the sociodemographic data of the study will be collected using an Information Form containing questions about the child's age, gender, and descriptive characteristics such as whether they have previously had an intravenous catheter inserted.

Other

MeasureTime frameDescription
2. Outcome MeasuresFor children in both groups: Ten minutes before the intravenous procedure, during the procedure, and ten minutes after the procedure, both the child and the researcher will rate the child's pain using scales.Visual Pain Scale: The scale is a 10 cm line scaled from 1 to 10 to determine the severity of pain in children, with 10 representing maximum pain and 0 representing no pain. Patients are asked to mark a spot on the scale according to the pain they feel.
3. Outcome MeasuresFor children in both groups: Ten minutes before the intravenous procedure, during the procedure, and ten minutes after the procedure, both the child and the researcher will rate the child's anxiety using scales.Child Anxiety Scale-State (CAS-D): The scale is designed in the shape of a thermometer. Each horizontal line on the thermometer represents one point, and the light bulb at the bottom represents 0 points. As you move upward, the score increases, with a maximum of 10 points. A score of 0 on the scale indicates no anxiety, while a score of 10 indicates the highest level of anxiety.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026