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Having a Blood DrawStress ballNCT05191901

The EFFECT of STRESS BALL DURING the PROCEDURE in CHILDREN

A study testing Stress Ball in people with Having a Blood Draw, run by Ayse Sonay Turkmen, Prof.Dr at 2 sites in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This research was planned in a Randomized Controlled Experimental Research design with Pre-Test-Post-Test Control Group in order to determine the effect of the stress ball squeezing technique applied to children aged 7-12 during the vascular access procedure on the level of fear and pain in children. Read more about this study

Who is it for?
Ages 7 to 12 yearsHealthy volunteers can take part
Conditions the study is for
Having a Blood Draw
What is being tested?
Stress Ball
Could I receive a placebo?
No, everyone receives an active treatment
How many people
116 participants
Where
2 sitesTurkey (Türkiye)
Study dates
14 Mar 2022to 20 May 2022
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 7 to 12 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • The child is between the ages of 7-12
  • Absence of pain (due to disease, drug side effects, distension)
  • Absence of any physical or mental illness
  • Being able to communicate and being open to communication
  • No history of ischemic epilepsy, migraine or vestibular disorder
  • No long-term illness.
Show all 13Show fewer
  • Absence of a regularly used medication
  • Not taking analgesics in the last six hours
  • Hospitalization for diagnosis or treatment
  • Vascular access is performed by the same nurse,
  • Single way vascular access
  • The child and parent speak and understand Turkish comfortably,
  • The child and his parents do not accept to participate in the study, and they do not have a speech or vision disorder.

Who cannot join

  • who do not meet the inclusion criteria.

Trial locations and contacts

2 sites in 1 country.

Turkey (Türkiye)2 sites
  • KaramanogluMehmetbeyU

    Karaman, Turkey, 70100

  • Karamanoglu Mehmetbey University

    Karaman

Other trials in Turkey (Türkiye)

About this study

Official title: The EFFECT of STRESS BALL on REDUCING the FEAR and PAIN OCCURRENT DURING the PROCEDURE in CHILDREN

This research was planned in a Randomized Controlled Experimental Research design with Pre-Test-Post-Test Control Group in order to determine the effect of the stress ball squeezing technique applied to children aged 7-12 during the vascular access procedure on the level of fear and pain in children. The data of the study were obtained from children aged 7-12 who came to the Karaman Training and Research Hospital Pediatrics Service between August 1 and October 31, 2020. The sample size was determined as 116 children in total, 58 children for each group. "Interview and Observation Form, Children's Fear Scale (CFS), Wong-Baker Faces, Stress Ball and Stopwatch" were used for data collection.

In order to evaluate whether the research is ethically appropriate, an application was made to the Ethics Committee of Karamanoğlu Mehmetbey University School of Health Sciences and the necessary permission was obtained. Written permission was obtained from the Chief Physician of Karaman Training and Research Hospital in order to conduct the study in the Child Health and Diseases Service of Karaman Training and Research Hospital.

Statistical analyzes of the study will be done in SPSS 21.0 package program. Number, percentage, mean and standard deviation values will be used from descriptive analyses. In the analysis of differences between groups, independent groups t test, paired t test, Anova, Mann Whitney U and Kruskal Wallis tests will be used. Tukey or Duncon tests will be used for further analysis. The change in the post-procedural pain level of children according to some variables will be evaluated with multiple and simple regression analyses. Significance level will be accepted as p<0.05.

Read the detailed description

Dependent variable: Children's level of pain and fear Independent variable: Stress ball, demographics, previous painful transaction experience Randomization of control and stress ball groups; The status of the children to be included in the study in the control or stress ball group was determined by using "stratification and randomization methods with blocks". In the literature, it has been reported that gender and fear of interventional procedures are among the factors affecting the fear and anxiety experienced by children in interventional procedures (Törüner \& Büyükgönenç, 2012; Çavuşoğlu, 2013). Accordingly, stratified and block randomization will be applied to the children as "girl and boy" for the gender variable and "afraid and not afraid" for the fear of the procedure. 58 children will be included in each of the research groups. During the data collection process, each child and family will be taken to the invasive procedure room individually. This will prevent children from meeting with each other.

The determined layers were created by the statistician as codes obtained from a permutation-based computer program (https://www.randomizer.org). At the beginning of the study, which letter would be the stress ball or the control group was determined by the closed opaque envelope method, and the letter A was used for the stress ball group and the letter B was used for the control group.

Blinding: Single blinding (participants) will be used in the study. Participants will not be told whether they are in a stress ball or control group. A separate informed consent form will be created and approved for each group. In order to prevent children and parents from encountering each other, information will be given in the closed operation room and their consent will be obtained. Each child will be taken to a separate room with one of their parents. It will be ensured that no child is waiting near the door for invasive intervention.

Hypotheses H0: The stress ball applied during the vascular access procedure does not affect the fear and pain levels of children.

H1: The stress ball applied during the venipuncture procedure affects the children's fear levels H2: The stress ball applied during the vascular access procedure affects the pain levels of children.

H3: The stress ball applied during the venipuncture procedure affects the satisfaction of children, parents and nurses.

The research will be carried out in the following order.

  1. Since the vascular access procedure will be performed by a single nurse, the children who are admitted to the service during the working day and time of the determined nurse and those whose parents are volunteers will be included in the study. Before the data collection phase, children and parents who meet the sample selection criteria of the research will be informed about the purpose and content of the research, and verbal and written consent will be obtained from their parents.
  2. Materials will be prepared beforehand (data collection tools, stress ball, stopwatch).
  3. Individual characteristics will be obtained from children and family members and recorded in the interview and observation form. Before the procedure, the fear level of children about the procedure will be recorded by asking the child, parent and observer separately using the Children's Fear Scale (CFS).
  4. The status of the child in the stress ball or control group will be determined by using layer sets.
  5. Children in the control group will be taken to the invasive procedure room and a parent will be with the child during the vascular access procedure. During the procedure, as soon as the children start to cry, the stopwatch will be started and will continue to run throughout the crying. After the procedure, the child's fear (Children's Fear Scale (CFS)) and pain (Wong-Baker FACES) related to the procedure will be evaluated separately by the child, parent and observer and recorded in the form.
  6. Children in the stress ball group will be asked to hold and squeeze the stress ball in their untreated hands before starting the vascular access process. A parent will be provided with the child during the procedure. A few seconds after the child starts squeezing the ball, the vascular access process will be started. The child will be asked to continue the process of squeezing the ball until the intravenous access is completed. During the procedure, as soon as the children begin to cry, the stopwatch will be started and will continue to run throughout the crying. After the procedure, the child's fear (Children's Fear Scale (CFS)) and pain (Wong-Baker FACES) related to the procedure will be evaluated separately by the child, parent and observer and recorded in the form.
Being tested
Stress Ball
Keywords
Pain, Turning Attention, Establishing intravascular access, Fear
Medical subject headings
Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Stress BallOther

    Reducing pain and fear by squeezing a stress ball during the blood draw procedure.

Study groups in NCT05191901
Study groupRoleWhat they receive
stress ball groupExperimentalNot described
Receives: Other: Stress Ball
control groupNo interventionNot described

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Pain scores

    Measured: 5 minutes

  2. Fear scores

    Measured: 5 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted14 Jan 2022
  2. Study start14 Mar 2022
  3. Primary completion30 Apr 2022
  4. Study completion20 May 2022

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
116 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05191901
Sponsor's protocol ID
Stress Ball
Acronym
Stress ball
Status last verified
May 2022
First submitted
20 Dec 2021
Last updated
10 Jan 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Stress Ball in people with Having a Blood Draw, run by Ayse Sonay Turkmen, Prof.Dr at 2 sites in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 10 Jan 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Pain scores (time frame: 5 minutes). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Jan 2025.

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