Coolsense and Buzzy Use on Pain Score and Anxiety Level During Insulin Injection Application

Ankara Yildirim Beyazıt University

Status: Completed

Conditions: Type 1 Diabetes Mellitus; Injection Site Coldness; Injection Fear; Pediatric Disease; Pain; Nurse's Role

Treatments: Device: Coolsense and Buzzy

Study type: Interventional

Funder types: Other

Identifiers

NCT06369649

COOLSENSE-1

Details and patient eligibility

About

This study aims to determine the effect of using Coolsense, which is created using the proven effect of cold application during insulin injection, and Buzzy, which is a combination of vibration and cold application, in reducing pain and anxiety in children diagnosed with Type 1 diabetes mellitus.This randomized controlled clinical study is planned to be conducted between 05.2024-12.2025 with 147 participants between the ages of 6-12. Participants will be divided into three groups according to the randomization method: buzzy group (n = 49), coolsense group (n = 49) and control group (n = 49). Participants in the Coolsense group will receive a cold application using the coolsense device for 5 seconds before the injection. Participants in the Buzzy group will be subjected to vibration and cold application 30-60 seconds before the procedure. Participants in the control group will continue the clinic's standard procedure. Changes in participants' pain score and fear level, heart rate, blood pressure, respiratory rate and oxygen saturation will be measured at three time points: immediately before and after the procedure. Data descriptive information form, application registration form, Facial Expressions Pain Scale (FPS-R) and Child Fear Scale (CFS) will be used. The collected data will be analyzed using SPSS 15 software. The main questions it aims to answer:

• Does buzzy and coolsense application have an effect the pain score of children during the insülin injection?
• Does buzzy and coolsense application have an effect the fear score of children during the insülin injection?

Full description

Children between the ages of 6-10, who is diagnosed at least 2 weeks ago, will be included in the study.Patients with intellectual or neurological disabilities, Raynaud syndrome or sickle cell anemia will excluded from the study.

Enrollment: 90 patients

Sex: All

Ages: 6 to 10 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Being an inpatient in the Pediatric Endocrinology Service
• Having a diagnosis of Type 1 Diabetes Mellitus (no more than 6 months have passed since the diagnosis) receiving insulin therapy
• Being in the 6-10 age group.
• Having no pain before the application (getting 0 points on the pain scale).
• Blood sugar level above 80 mg/dl
• Having parental permission
• The child's willingness to participate in the research
• Not having used any medication that would have an analgesic effect in the last 24 hours before application.
• The child does not have a mental or neurological disability
• Not having any disease that causes sensitivity to cold, such as Reynaud's syndrome or sickle cell anemia.
• The child must be conscious and have no communication problems
• The child and the parent must be able to speak Turkish

Exclusion criteria

• Being younger than 6 years old and older than 12 years old
• Not having a diagnosis of Type 1 Diabetes
• Presence of pain before application
• Blood glucose level should be below 80 mg/dl before application
• The person or the parent does not agree to participate in the research.
• Having a disease that causes chronic pain
• Presence of any incision or scar tissue in the area to be injected

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

90 participants in 3 patient groups

Coolsense

Experimental group

Description:

For children in this group, the standard approach of the clinic will be applied first. The researcher will apply scales to the child before the procedure, the Child-Parent Information Form to the parents, and the child, parent and independent observer before and after the procedure. The patient's physiological parameters will be recorded by the nurse performing the procedure before, during and after the procedure. The device, which is removed from the freezer just before the injection, will be applied by the researcher to the skin surface where the procedure will be performed for approximately 5-10 seconds before the injection, and then the injection will be performed.

Treatment:

Device: Coolsense and Buzzy

Buzzy

Experimental group

Description:

For children in this group, the standard approach of the clinic will be applied first. The researcher will apply scales to the child before the procedure, the Child-Parent Information Form to the parents, and the child, parent and independent observer before and after the procedure. The patient's physiological parameters will be recorded by the nurse performing the procedure before, during and after the procedure. The device, which will be removed from the freezer just before the injection, will be placed by the researcher in contact with the skin, 3 to 5 cm above the injection site. Buzzy will be started 30-60 seconds before the process and will continue until the end of the process.

Treatment:

Device: Coolsense and Buzzy

Control

No Intervention group

Description:

For children in this group, the standard approach of the clinic will be applied first. The researcher will apply scales to the child before the procedure, the Child-Parent Information Form to the parents, and the child, parent and independent observer before and after the procedure. The patient's physiological parameters will be recorded by the nurse performing the procedure before, during and after the procedure.