The Efficiency of Chest Physiotherapy Applied in a Different Order

  • STATUS
    Recruiting
  • days left to enroll
    15
  • participants needed
    52
  • sponsor
    Selmin Kose
Updated on 8 August 2022

Summary

This study intends to compare the impact of chest physiotherapy applied with two different methods on physiologic parameters in children hospitalized in the intensive care unit. In the intensive care unit where the study was conducted, the patients who have a respiratory disorder and receive supplemental oxygen therapy with non-invasive mechanical ventilation or an oxygen mask are first administered an inhaler drug therapy placed in the physician's order. It is followed by chest physiotherapy and then oropharyngeal and nasopharyngeal aspiration. However, in practice rendered by the researcher, it is suggested that when chest physiotherapy and aspiration are administered in the first place and then followed by an inhaler drug therapy, it might have a more positive impact on the patient's physiologic parameters. For this reason, it is intended to compare the efficiency of chest physiotherapy applied in a different order.

Description

42 children who complied with the inclusion criteria will be included in the study. The mother or father of the children hospitalized in the pediatric intensive care unit of the hospital where the study is conducted will be given information about the study and asked to sign the "Informed Voluntary Consent Form". After the family's approval, they will be asked to fill out the "Parent Introductory Information Form".

The randomization method will be used to create the control group and the study group. Children to be included in the study will be placed in the groups with the randomized controlled method with 21 children in each group. The randomization of the study will be made with the online program available at the URL address https://www.randomizer.org/. Before entering the sample size in the program, lots will be drawn, and the 1st set will be assigned to the control group, and the 2nd set will be assigned to the study group. In order to determine in which group the children involved in the study will be placed, numbers from 1 to 42 will be entered into the program without repetition. Children that will constitute the study group through the program will be randomly distributed into 2 groups.

The control group (n=21) will be administered the inhaler drug routinely administered in the intensive care unit where the study is conducted and then receive chest physiotherapy (tapotement or vibration), then nasopharyngeal and oropharyngeal aspiration. The study group (n=21) will first receive chest physiotherapy (tapotement or vibration) and aspiration, followed by inhaler drug therapy.

The "Patient Data Collection Forms" of both groups will be filled out. Chest physiotherapy will follow the "Tapotement and Vibration Application Procedure," and aspiration will follow the "Nasopharyngeal and Oropharyngeal Aspiration Application Procedure". The "Patient Physiologic Parameter Assessment Form" information will be recorded before the application and 20 minutes after the application. It is known that the stress hormones epinephrine and norepinephrine half-life is 1-3 minutes, and it is believed that after a stressful invasive intervention, the release of stress hormones increases but turns back to their normal levels in 15-20 minutes (Puntillo et al. 2001). Based on this information, vital findings will be recorded in the "Patient Physiologic Parameter Assessment Form" after 20 minutes.

Obtained data will be evaluated using necessary statistical tests in the computer environment. Evaluation methods will be selected considering if data is distributed homogenously. If it has a homogenous distribution, parametric tests will be used. If it does not have a homogenous distribution, non-parametric methods will be used.

Details
Condition Respiratory Disease
Treatment Chest Physiotherapy- Aspiration- Inhaler drugs group
Clinical Study IdentifierNCT05022082
SponsorSelmin Kose
Last Modified on8 August 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Hospitalized patients at Cerrahpaşa Faculty of Medicine Pediatric Intensive Care Unit 1
Aged between 1 months-6 years
Having been in intensive care for at least two days
Concious pediatric patient
Receiving supplemental oxygen therapy with non-invasive mechanical ventilation or an oxygen mask
Being administered chest physiotherapy (Tapotement or Vibration)
Being administered oropharyngeal and nasopharyngeal aspiration
Inhaler drug therapy included in the patient's order
Parents, volunteering for the study

Exclusion Criteria

Parents not volunteering for the study
Patients younger than 1-month or older than 6-years old
Not receiving supplemental oxygen therapy with non-invasive mechanical ventilation or an oxygen mask
Not being administered oropharyngeal and nasopharyngeal aspiration
Inhaler drug therapy is not included in the physician's order
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