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Nursing CariesNCT06482710

The Effect of Breathing Exercise With Pinwheel on the Quality of Life in Children With Cystic Fibrosis Disease

A study testing Pinwheel in people with Nursing Caries and Breathing Exercise, run by Maltepe University at 1 site 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 study aims to present the results of the effect of pinwheel breathing exercises on the quality of life in children with Cystic Fibrosis (CF). In this randomized controlled study, 81 children with CF who were being monitored by the treatment team in the pediatric chest polyclinic of a state hospital and meeting… Read more about this study

Who is it for?
Ages 6 to 11 years
Conditions the study is for
Nursing Caries, Breathing Exercise
What is being tested?
Pinwheel
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
70 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Dec 2023to 31 May 2024
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 6 to 11 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • 6-11 years old
  • Those diagnosed with cystic fibrosis at least 1 year ago
  • Those who were accompanied by their parents during the research
  • Those who can speak and understand Turkish
  • Children whose parents voluntarily accepted the study were included in the study.

Who cannot join

  • Those with mental, auditory and visual problems
  • Those with physical disabilities (limitation of movement in the use of upper extremities and congenital muscle diseases)
  • Those who stopped doing breathing exercises with the pinwheel during the research follow-up period
  • Children with a clinical course of acute exacerbation (the presence of at least a few of the following signs and symptoms: cough with high fever, increased sputum quantity, bloody sputum, more than 10% decrease in pulmonary function test value (FEV1), fatigue, weight loss, dyspnea) were not included in the study

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Maltepe University School of Nursing Istanbul, Maltepe, Turkey.

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: The Effect of Breathing Exercise With Pinwheel on the Quality of Life in Children With Cystic Fibrosis Disease: A Prospective Randomized Controlled Study

This study aims to present the results of the effect of pinwheel breathing exercises on the quality of life in children with Cystic Fibrosis (CF). In this randomized controlled study, 81 children with CF who were being monitored by the treatment team in the pediatric chest polyclinic of a state hospital and meeting the inclusion criteria were divided equally into two groups. The children in the first group (intervention group) were instructed to perform breathing exercises with a pinwheel twice a day, at a convenient time in the morning and in the evening, every day for 3 months in their own homes according to the Breathing Exercise Tracking Form (BETF) and to fill in the required fields of the form during this process. The children in the second group (control group) did not perform the pinwheel breathing exercise. The quality of life of the children in both groups was evaluated with the Cystic Fibrosis Questionnaire-Revised (CFQ-R) (age group 6-11).

Read the detailed description

Cystic Fibrosis (CF) is an autosomal recessive genetic disorder that affects many organs simultaneously. The sinuses, lungs, intestines, pancreas, gallbladder, liver, reproductive organs, and sweat glands are affected by CF. The treatment of children with CF includes medication, diet therapy, pancreatic enzyme therapy, chest physiotherapy, and lung transplantation. When chest physiotherapy is not performed effectively and regularly, children have increased hospital admissions, prolonged hospitalization, restricted daily activities, loss of independence, decreased quality of life, and social isolation. The aim of this randomized controlled trial was to present the results of the effect of pinwheel breathing exercises on the quality of life in children with CF.

METHODS This study was conducted in a single-center, prospective randomized controlled design. The sample size of the study was calculated using G*Power 3.1.9.2 (Heinrich Heine University Düsseldorf, Germany). The sample size was found to be 35 for each group. The study authors considered possible sample losses during the study process. It was determined to conduct the study with a total of 70 children. There were 35 children in each group (intervention and control groups). Between January and April 2024, 81 children aged 6-11 years with CF who were enrolled in the Pediatric Chest Outpatient Clinic of Marmara University Pendik Training and Research Hospital were included in this study. Among these children, 70 children who met the inclusion criteria were included. Children who did not come to the Pediatric Chest Outpatient Clinic for routine controls (n = 10) and children whose parents refused to participate in the study (n = 1) were excluded.

Procedures:

Participants were assigned to their respective groups, and the pinwheels to be given to the intervention group were placed in locations to be used in the interviews. Vital signs, Child Health Status Diagnosis Form (CHSDF), Cystic Fibrosis Questionnaire Revised (CFQ-R), and Breathing Exercise Practice and Follow-up Form (BEPFF) and all records were documented by the first researcher. The first researcher has 2.5 years of experience as a pediatric intensive care and pediatric ward nurse. The pediatric chest outpatient clinic works in a single shift during the day (08:00-16:00). In this study, the following procedures were performed respectively. Initial assessments of children with CF registered in the pediatric chest outpatient clinic were performed between 08:00 and 16:00 at their own scheduled appointment hours. The parents of the children in the intervention group were informed about all stages of the research process and provided verbal and written consent. The children were randomly assigned to the groups by the simple randomization method. Randomization was made according to the daily examination appointment order of the pediatric pulmonology outpatient clinic of the hospital. Children with an odd number of appointments were included in the intervention group, and those with an even number were included in the control group. For example, the child whose examination appointment was in the 1st place was included in the intervention group, and the child whose appointment was in the 2nd place was included in the control group. This method was repeated until the sample size was reached. In this study, all assessments were performed in the same way for children in the intervention and control groups. Vital signs, pulmonary function test values, and quality of life data of the children were re-evaluated at various time points. These time points were: before the intervention and the first appointment day after the intervention (at least 3 months). Before the intervention covers the interval between the appointments scheduled between 08:00 and 16:00 for the child's first evaluation. After the intervention covers the interval between the appointments scheduled from 08:00 to 16:00 for the child's second evaluation after 3 months. Factors determining children's quality of life were evaluated twice, before and after the intervention. The vital signs and pulmonary function test values of the children were measured once on the day of the intervention (between 08:00 and 16:00 appointment hours). Console-type pulse oximeter and pulmonary function test device (spirometer) were used. All data except the vital signs of the children were asked to the mothers and children face to face, and their answers were recorded in the CFQ-R.

Instruments:

Data were collected using the Child Health Status Diagnostic Form (CHSDF), the Cystic Fibrosis Questionnaire Revised (CFQ-R), and the Breathing Exercise Practice and Follow-up Form (BEPFF). The CFQ-R and BEPFF were developed by the researcher and the counselor after reviewing the relevant literature. Child Health Status Diagnosis Form (CHSDF): In the first part of this form, there are three open-ended questions about the child's date of diagnosis, other diseases, and medications that the child is constantly taking. The second part of the form consists of three sections. These sections include the initial and second assessments. If the initial assessment is to be made, the initial assessment box will be filled in, and if the second assessment is to be made, the second assessment box will be filled in. The evaluation parameters for each section are specified. In this study, the CFQ-R form was used for the 6-11 age group. This form consists of two parts, and all questions are equally weighted. In the first part, there are five questions about the child's date of birth, gender, absence from school in the last two weeks due to vacation or non-health-related reasons, racial origin, and grade level. In the second part, there are 35 questions assessing children's physical functioning (questions 1-6), emotional functioning (questions 7-14), social functioning (questions 15,16,19), treatment burden (questions 17,18,29), respiratory (questions 31-34), and digestive findings (question 35) in the last two weeks.

The scale score is made with the online application on https://cfqr-app.netlify.app/#/questionnaire prepared by Quittner et al. It is calculated by obtaining a score between 0-100 for each sub-heading. Higher scores indicate better quality of life. Breathing Exercise Practice and Follow-up Form (BEPFF): This form is used to describe how the children in the study group should perform the breathing exercise during the breathing exercise with the pinwheel. It is composed of seven rows with instructions. Opposite each row, there are seven columns with 2-week evaluation times, and two columns for each evaluation time to be marked "morning" and "evening" were added. The boxes in front of the morning and evening breathing exercises were marked with a check: "✓". In the study, a pinwheel was used to ensure and improve the continuity of children's breathing exercises and to increase lung capacity. This pinwheel has a structure consisting of multiple small wings mounted on a handle. It consists of 8 wings with an 18 cm diameter and is 38 cm in total length. The pinwheel is usually made of durable paper material, so it can be used repeatedly. The easy rotating structure of the pinwheel makes it simple and easy for children to use. These features ensure that children aged three and above can easily use the pinwheel.

Intervention:

Children in the study and control groups enrolled in the pediatric chest outpatient clinic were monitored with a pulse oximetry device and pulmonary function test device. Vital signs and pulmonary function test values were measured and recorded at their scheduled appointments between 08:00 and 16:00 on the day of the intervention. Before the intervention (initial assessment), the children's information was recorded in the pretest CFQ-R questionnaire. Each child in the intervention group was given a pinwheel at their appointment time. The child was given the BEPFF and instructions on how to use the form were explained in detail. In line with the BEPFF, the child was told to sit in a chair suitably, remove their surgical mask, and take the pinwheel in the hand that they dominantly use. In line with BEPFF, the child was instructed to perform the breathing exercise with the pinwheel, and whether the practice was performed correctly was evaluated in detail. The child repeated the breathing exercise several times in order to perform it correctly.

The child who was observed to perform the breathing exercise correctly in accordance with the BEPFF was instructed to perform this exercise twice a day, in the morning and in the evening, for 3 months at home. In order to encourage the children to continue the breathing exercises regularly, weekly reminder messages were sent via phone messaging for 3 months. Children in the control group were not given a pinwheel, and BEPFF was not applied. Children in this group continued their routine treatment processes. After the intervention evaluations (second evaluation) of the children in the intervention and control groups were conducted at the follow-up appointments scheduled 3 months later. Vital signs and pulmonary function test values were measured and recorded at their scheduled appointments between 08:00 and 16:00. Factors affecting quality of life were asked face-to-face, and the answers were recorded on the post-test CFQ-R questionnaire

Being tested
Pinwheel
Keywords
Child, Cystic fibrosis, Breathing exercise, Pinwheel, Therapeutic play, Quality of life
Medical subject headings
Cystic Fibrosis

What participants receive

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

  • PinwheelDevice

    The children in the intervention group were given breathing exercises with pinwheels.

Study groups in NCT06482710
Study groupRoleWhat they receive
Pinwheel GroupExperimentalChildren in the intervention group with CF were given pinwheel breathing exercises.
Receives: Device: Pinwheel
Control GroupNo interventionThe children in the control group were not given pinwheel breathing exercises and continued with their own breathing exercise routines.

What is being measured

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

  1. Identifying children's quality of life

    The child's routine implementation and follow-up of the breathing exercise was assessed.

    Measured: 3 months of routine implementation and follow-up of breathing exercise and change in quality of life of children.

Timeline

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

  1. First posted1 Jul 2024
  2. Study start1 Dec 2023
  3. Primary completion30 Mar 2024
  4. Study completion31 May 2024

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
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
70 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06482710
Sponsor's protocol ID
2024/05-26
Status last verified
Jul 2024
First submitted
26 Jun 2024
Last updated
3 Jul 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Pinwheel in people with Nursing Caries and Breathing Exercise, run by Maltepe University at 1 site 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 5 inclusion and 4 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 3 Jul 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site 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?

Identifying children's quality of life (time frame: 3 months of routine implementation and follow-up of breathing exercise and change in quality of life of children.). 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 3 Jul 2024.

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