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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04513873
Other study ID # 2019/37
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 18, 2019
Est. completion date March 28, 2019

Study information

Verified date August 2020
Source Afyonkarahisar University of Health Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to investigate the effect of diverting the children's attention to a different point during phlebotomy which is an invasive procedure with acute pain. This is a randomized controlled experimental study. The study was conducted with two groups: the intervention group (n=127) and the control group (n=129). The control group was applied to standard phlebotomy procedures. In contrast, the intervention group had a piece of equipment that looks like a blood tube in front of them during the phlebotomy process to divert their attention from the phlebotomy process to the equipment.


Description:

The equipment used for the intervention group was designed and developed by the researchers with the project support of TÜBİTAK BİDEB 2209A in 2016. It is an equipment that looks like a blood tube with a fixed arm on the right and a moving arm on the left with a total height of 80 cm. It has some answers to common questions of parents as well as the key concerns of the children " Will it hurt me?"


Recruitment information / eligibility

Status Completed
Enrollment 256
Est. completion date March 28, 2019
Est. primary completion date March 28, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 7 Years to 12 Years
Eligibility Inclusion Criteria:

- making a request for the phlebotomy

- being in the 7-12 age group

- having the consent of the parent

- willing to participate in the research

- with the history of invasive procedure

- not using any medication with analgesic effect in the last 12 hours

- without any communication barriers of either child or the parent

- with a normal level of consciousness during the process

- without the history of passing out during the phlebotomy

Exclusion Criteria:

- not being in the 7-12 age group

- not having the consent of the parent

- not willing to participate in the research

- without the history of invasive procedure

- had medication with analgesic effect in the last 12 hours

- with communication barriers of either child or the parent

- with an abnormal level of consciousness during the process

- with the history of passing out during the phlebotomy

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Equipment to divert the focus of children
The equipment was placed in an area where the children would be able to see easily during the blood collection process. It was turned on as soon as the children sat on to the chair where the process would take place to divert the focus of the children at the equipment.

Locations

Country Name City State
Turkey Manavgat State Hospital Antalya Manavgat

Sponsors (1)

Lead Sponsor Collaborator
Afyonkarahisar University of Health Sciences

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assessment of Children's Anxiety Level Change Children's Fear Scale is an instrument with five different face images changing from neutral (0= no fear) to most scared (4= with the most fear) to evaluate the scare level of the children during the procedure. Twice ( Immediately after the procedure and 14 days after the procedure)
Secondary Revised Face Pain Scale (FPS-R) The FPS-R is a scale to measure how children feel in their inner world than how their faces look. It is designed on the widely accepted 0-to-10 metric according to the chosen face. "0" equals "No pain" and "10" equals "Very much pain." Twice ( During the procedure and 5-10 minutes after the procedure)