Bed Baths' Impact on Blood Gases and Vital Signs in Children

March 7, 2025 updated by: Dr. Zübeyde KORKMAZ, Nuh Naci Yazgan University

Influence of Bed Baths on Blood Gases and Vital Signs Given Under Heat to Children: Randomized Cross-Over Study

Study Overview:

This randomized cross-over study investigated the effects of bed baths on the vital signs and blood gas values of children. The children received two bed baths: one under a heater and the other at room temperature. The order of the bed baths was randomized.

Methods:

The study involved children aged 1-36 months hospitalized in the Pediatric Intensive Care Unit (PICU). The bed baths were administered by a research nurse and assistant staff between 16:00 and 24:00 on weekends. The vital signs and capillary blood gas values (pH, PaO2, PaCO2, HCO3-) were measured three times: before, immediately after, and one hour after the bath. Data on heart rate, blood pressure, SpO2, and blood gas values were collected using specialized equipment.

Heating and Bathing Process:

For the heated bed bath, two heaters were positioned 50-60 cm above the child's bed, and the bath was conducted using soapy water at 37-40°C, followed by clear water.

Population:

The study was conducted in the PICU of a children's hospital, including children aged 1-36 months who were on mechanical ventilation, had normal body temperatures, and did not have chronic diseases. A total of 12 children participated over a period of two years.

Statistical Analysis:

Data were analyzed using IBM SPSS Statistics. Descriptive statistics such as percentages, averages, and standard deviations were used. The normality of the data was assessed, and repeated measurements were analyzed using ANOVA.

Study Overview

Status

Completed

Conditions

Detailed Description

Methods/Methodology This study was conducted in a randomized cross-over study. Study Design and Procedures In the study, children were given bed baths twice. One of the bed baths was done under heater and the other at room temperature. Which bed bath would be given first was determined by simple randomization (by lottery method). The bed baths of children participating in the study were given by a research nurse and an assistant staff. Children's bed baths are routinely given between 16:00 and 24:00 on weekends. Children who need a bed bath on weekdays are given a wiping bath by the caring nurse. The bed bath was performed in approximately at 21-240C room temperature in 20 to 25 minutes, with soapy water at 37-400C followed by clear water. The bed baths which were performed at under two heaters located 50-60 centimeters away from the bed of the children.

Measurements Applied at the Clinic The vital signs and capillary (right hand, middle finger) blood gas values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath.

  1. Heart Rate Heart rates were measured using a PVM-2701 monitor (Nihon Kohden Corp., Tokyo, Japan).
  2. Blood Pressure Blood pressures were measured manually over a period of one minute by a nursing team.
  3. pH, PaO2, PaCO2 and HCO3- Measurements For all patients, pH, PaO2, PaCO2 and HCO3- measurements were recorded from capillary blood samples, using an ABL800 FLLEX blood gas analyzer (Radiometer Medical A/S, Brønshøj, Denmark).
  4. SpO2 Measurements SpO2 was measured non-invasively using a PVM-2701 monitor (Nihon Kohden, Corp.). The saturation probe was applied to the patient's right palm. Daily measurements were recorded throughout each patient's stay in the Pediatric Intensive Care Unit (PICU).
  5. Patient Warming To heat the environment during bathing, the heating devices (Patient Warming System, Nellcor) were fixed 50-60 centimeters upwards from the bed on two sides, both left and right Population and Samples The study was conducted in the PICU of the Children's Health Hospital affiliated with the Central Anatolian Public Hospitals Association. The intensive care unit where the study was conducted is an 8-bed 3rd degree PICU that cares for children between the ages of 1 month and 18 years. The data collection process took 2 years due to the long-term hospitalization of children in the unit and only children aged 1-36 months (Because of clinical nurses observed that the vital signs and blood gas values of children with mechanical ventilators for 1-36 months were affected after bedside bathing and that mechanical ventilator settings were changed) included in the study, and 12 children were reached in a two-year period. Children who are hospitalized for respiratory failures and in mechanical ventilators, not given Total Parenterally Nutrient, are normal body temperatures, are not suffering from any chronic diseases, and bathing would not cause problems was included.

Data Management and Statistical Analysis The data was evaluated in the IBM SPSS Statistics Standard Concurrent User V 25 (IBM Corp., Armonk, NY, USA) statistical package program. Number of units (n), percentage (%), average ± standard deviation (¯x±ss), median (M), and 25-75. percentile is given as descriptive statistics. Normal distribution of data regarding the numeric variables was evaluated with Q-Q plots and Shapiro-Wilk test for normality. Repeated measurements were variance analyzed (ANOVA).

Study Type

Interventional

Enrollment (Actual)

12

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Children who are hospitalized for respiratory failures and in mechanical ventilators,
  • having normal body temperatures

Exclusion Criteria:

  • Total Parenterally Nutrition
  • any chronic diseases
  • any disease or condition which bathing would cause problems

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: Randomized
  • Interventional Model: Crossover Assignment

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: bed bath
This practice is a complementary and supportive care intervention.
Experimental: bed bath with heat
This practice is a complementary and supportive care intervention.In detail, this bed baths which were performed at under two heaters located 50-60 centimeters away from the bed of the children.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
temperature measure
Time Frame: The bady temperature values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
Celcius
The bady temperature values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
Pulse
Time Frame: The heart pulse values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
per minute
The heart pulse values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
blood pressure
Time Frame: The blood pressure values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath.The values were measured three times in each bed bath, for a total of six times.
mmHg
The blood pressure values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath.The values were measured three times in each bed bath, for a total of six times.
oxygen saturation
Time Frame: The oxygen saturation values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
The oxygen saturation values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
blood pH
Time Frame: The capillary blood pH values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
pH
The capillary blood pH values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
PaO2
Time Frame: The capillary blood PaO2 values were evaluated for total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
The capillary blood PaO2 values were evaluated for total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath. The values were measured three times in each bed bath, for a total of six times.
PaCO2
Time Frame: The capillary blood PaCO2 values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath.The values were measured three times in each bed bath, for total of six times.
The capillary blood PaCO2 values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bath.The values were measured three times in each bed bath, for total of six times.
HCO3-
Time Frame: The capillary blood HCO3- values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bathThe values were measured three times in each bed bath, for total of six times.
mEq/L
The capillary blood HCO3- values were evaluated for a total of three times; five minutes before the bed bath, five minutes after the bed bath, and an hour after the bed bathThe values were measured three times in each bed bath, for total of six times.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 15, 2015

Primary Completion (Actual)

December 30, 2017

Study Completion (Actual)

March 15, 2018

Study Registration Dates

First Submitted

February 25, 2025

First Submitted That Met QC Criteria

March 7, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 7, 2025

Last Verified

March 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • NuhNaciYazganU3

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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