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The Effect of Two Different Bathing Methods on Vital Signs and Comfort in PICU:Bath Trial

I

Izmir Katip Celebi University

Status

Enrolling

Conditions

Comfort
Vital Sign Monitoring

Study type

Observational

Funder types

Other

Identifiers

NCT06836947
006
ikçü (Other Identifier)

Details and patient eligibility

About

The study was planned to be conducted and completed within 6 months after ethics committee approval was obtained. The study is a prospective, quasi-experimental study.

The population of the study will consist of children who are hospitalized in the Pediatric Intensive Care Unit of SBÜ. İzmir Dr. Behçet Uz Pediatric Diseases and Surgery Training and Research Hospital. The vital signs and comfort of the children of the parents who agreed to participate in the study will be measured before bathing (baseline) and care will be taken to ensure that they are similar in both groups.

Children in the study will not be randomized. In the routine operation of the clinic, traditional bathing is performed once a week and wipe bathing is performed once every two days. Wipe bathing is performed at 36-37 degrees water with 10 ml of chlorhexidine in 200 ml of water. Traditional bathing is also performed with 36-37 degrees water in bed or in the bathtub. In the study, no intervention will be performed and the outcomes will be measured and compared with each other before and after both bathing procedures.

Physiologic parameters including respiratory rate, pulse rate, oxygen saturation and comfort levels of newborns just before, during and after the bathing process (1st and 5th minute) will be evaluated and compared with each other. To avoid bias in the study, all bathing procedures will be performed by Specialist Nurse Esat Erdem GÖKPINAR.

Translated with DeepL.com (free version)

Full description

The study was planned to be conducted and completed within 6 months after ethics committee approval was obtained. The study is a prospective, quasi-experimental study.

The population of the study will consist of children who are hospitalized in the Pediatric Intensive Care Unit of SBÜ. İzmir Dr. Behçet Uz Pediatric Diseases and Surgery Training and Research Hospital. The vital signs and comfort of the children of the parents who agreed to participate in the study will be measured before bathing (baseline) and care will be taken to ensure that they are similar in both groups.

Children in the study will not be randomized. In the routine operation of the clinic, traditional bathing is performed once a week and wipe bathing is performed once every two days. Wipe bathing is performed at 36-37 degrees water with 10 ml of chlorhexidine in 200 ml of water. Traditional bathing is also performed with 36-37 degrees water in bed or in the bathtub. In the study, no intervention will be performed and the outcomes will be measured and compared with each other before and after both bathing procedures.

Physiologic parameters including respiratory rate, pulse rate, oxygen saturation and comfort levels of newborns just before, during and after the bathing process (1st and 5th minute) will be evaluated and compared with each other. To avoid bias in the study, all bathing procedures will be performed by Specialist Nurse Esat Erdem GÖKPINAR.

Translated with DeepL.com (free version)

Enrollment

52 estimated patients

Sex

All

Ages

28 days to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Being hospitalized in Behçet Uz Pediatric Intensive Care Unit
  2. No contraindications to bathing
  3. Parent's willingness to participate in the study

Exclusion criteria

  1. Having a contraindication to bathing
  2. Parents were not willing to participate in the study

Trial design

52 participants in 2 patient groups

Traditional Bathing Group
Description:
In traditional bathing, the patient is also bathed in bed with 36-37 degrees water.
Wipe Bathing Group
Description:
Wipe bathing is performed with 36-37 degrees water with 10 ml of chlorhexidine in 200 ml of water.

Trial contacts and locations

1

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Central trial contact

ESRA ARDAHAN AKGÜL, Ast. Prof

Data sourced from clinicaltrials.gov

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