Endotracheal AspirationNCT05331846
Breast Milk Odor on the Pain and Stress Level of the Newborn Endotracheal Aspiration Procedure
A study testing the smell of breast milk in people with Endotracheal Aspiration, run by Ataturk University at 1 site in Turkey (Türkiye).
Trial summary
Our study aims to determine the effect of breast milk odor on pain and stress in the application of endotracheal aspiration in newborns hospitalized in the Neonatal Intensive Care Unit. The research is planned experimentally with a pretest posttest randomized control group. Read more about this study
- Who is it for?
- Ages 1 day to 28 days
- Conditions the study is for
- Endotracheal Aspiration
- What is being tested?
- the smell of breast milk
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 88 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 19 Mar 2022to 19 Dec 2023
- 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 1 day to 28 days
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Being a term newborn,
- to be between 0-28 days,
- Receiving mechanical ventilation support,
- Not taking opioids or sedatives 4 hours before the procedure.
Who cannot join
- not be between 0-28 days,
- Not receiving mechanical ventilation support,
- Taking opioids or sedatives 4 hours before the procedure.
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Ataturk University Nursing of Faculty
Erzurum, Center, 25240
About this study
Official title: The Effect of Breast Milk Odor on the Pain and Stress Level of the Newborn During the Endotracheal Aspiration Procedure
Our study aims to determine the effect of breast milk odor on pain and stress in the application of endotracheal aspiration in newborns hospitalized in the Neonatal Intensive Care Unit. The research is planned experimentally with a pretest posttest randomized control group. The research will be carried out in Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022. The population of the study will consist of patients aged 30-28 days who were hospitalized in the Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022 and received mechanical ventilation treatment.
The research sample; Babies of families who are hospitalized on the dates specified with the probability sampling method and meet the research criteria and volunteer to participate in the research will be formed. Questionnaire Form, Neonatal Pain and Stress Assessment Scale, and Follow-up Form will be used to collect research data. The scent of breast milk will be used as an intervention tool in the research.
Read the detailed description
3.1. Type of Research The research is planned experimentally with a pretest posttest randomized control group.
3.2. Place and Time of Research The research will be carried out in Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022.
3.3. Population and Sample of the Research The population of the study will consist of patients aged 30-28 days who were hospitalized in the Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022 and received mechanical ventilation treatment.
The research sample; Babies of families who are hospitalized on the dates specified with the probability sampling method and meet the research criteria and volunteer to participate in the research will be formed. In this study, a priori power analysis was performed to determine the sample size. In the power analysis, Cohen's standard effect sizes reference method was chosen. In this case, in our study, for the t-test in independent groups in which the effect of sniffed breast milk on endotracheal aspiration application will be compared, it was determined that "80% power at the 95% confidence interval at the 0.05 significance level" could be reached if the study was conducted with a total of 80 participants in two groups with 40 participants in each group. In case of data loss, it was decided to collect data from a total of 88 individuals by including 10% backup sample to this number. Data will be collected at different times from newborns receiving invasive mechanical ventilation support in incubators in the Neonatal Intensive Care Unit. There is no interaction between the groups.
Inclusion Criteria for Research
- Being a term newborn,
- to be between 0-28 days,
- Receiving mechanical ventilation support,
- Not taking opioids or sedatives 4 hours before the procedure. 3.4. Data Collection Tools to be Used in the Research Questionnaire Form, Neonatal Pain and Stress Assessment Scale, and Follow-up Form will be used to collect research data. The scent of breast milk will be used as an intervention tool in the research.
Questionnaire Form: In this form, which was prepared by the researcher by examining the literature; There will be questions about the introductory features of the newborn.
ALPS Neo Neonatal Pain and Stress Rating Scale: The "Newborn Pain and Stress Rating Scale" was developed in 2014, based on the individualized developmental care of the newborn, in order to assess pain and stress in premature and term newborns. In 2017, this scale was adapted to Turkish and validity and reliability studies were conducted. ALPS Neo "Newborn Pain and Stress Assessment Scale" is a 3-point Likert-type scale consisting of 5 items, including "facial expression, breathing pattern, tone of extremities, hand/foot activities and activity level" of the newborn, and measurements are made by observation. As the scores obtained increase, pain and stress increase in the newborn. As a result of the evaluation, "3-5 points indicate the presence of mild pain and stress, and more than 5 points indicate the presence of severe pain and stress".
Follow-up Form: It is the form used to record the cardiorespiratory parameters (peak heart rate, oxygen saturation) of the newborn evaluated before, during and after the procedure, ALPS Neo pain scale, and crying time result.
Intervention Tool Used in Research Breast Milk Scent: Breast milk scent will be used as an intervention tool in the research. In the study, breast milk will be sniffed 5 minutes before endotracheal aspiration with the help of sterile sponge. As a non-pharmacological method, it is expected that the smell of breast milk will reduce the pain and stress felt during endotracheal aspiration in the newborn.
3.5. Data Collection The research data will be obtained from the babies of the parents who agreed to participate in the research after the researcher gave the parents of the patients preliminary information about the research (the purpose of the research, why the research was conducted, the attempt to relieve the neonatal pain with a non-pharmacological method, etc.) and their written consent was obtained.
Before the endotracheal aspiration attempt is made by the researcher to the experimental group, the patient will smell the breast milk scent with the help of a sterile sponge for 5 minutes.
The purpose of making the patient smell the breast milk; It is to reduce the pain level of the procedure to the minimum level by ensuring that the patient calms down. The researcher will have the patient smell breast milk for 5 minutes before the endotracheal aspiration procedure and will evaluate the patient with the "ALPS Neo Neonatal Pain and Stress Rating Scale" before, during and after the procedure. The control group will be routinely performed in the endotracheal aspiration procedure and will be evaluated with the "ALPS Neo Neonatal Pain and Stress Rating Scale" before, during and after the procedure.
3.6. Evaluation of Data The processing and statistical analysis of the collected data will be done with the analysis software called SPSS (Statistical Package for the Social Sciences) for Windows 20.0.
3.7. Ethical Principles of Research In order to carry out the research, official permission will be obtained from the relevant institution with ethical approval from the Ethics Committee. The purpose of the study will be explained to the parents of the babies with the research group criteria, the questions asked will be answered and their verbal and written consent will be obtained. Parents will be informed that the data collected during the research will be processed anonymously, confidentially, and will not be used outside of the study in question, and that they can leave the study whenever they wish. Since the research is based on the use of data obtained from humans, and therefore, due to the necessity of observing personal rights, the relevant ethical principles "Informed Consent", "Volunteerism" and "Protection of Confidentiality" will be followed.
- Conditions
- Endotracheal Aspiration
- Being tested
- the smell of breast milk
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
the smell of breast milkBehavioural
Smell of breast milk during endotracheal aspiration will reduce pain and stress
| Study group | Role | What they receive |
|---|---|---|
| SMELL OF BREAST MILK | Experimental | the smell of breast milk will reduce pain and stress Receives: Behavioral: the smell of breast milk |
| control | No intervention | pain and stress will not decrease |
What is being measured
The primary outcome is the main question the study is designed to answer.
ALPS Neo Neonatal Pain and Stress Rating Scale
In 2014, the "Newborn Pain and Stress Rating Scale" was developed based on the individualized developmental care of the newborn in order to evaluate pain and stress in premature and term newborns. In 2017, this scale was adapted to Turkish and validity and reliability studies were conducted. ALPS Neo "Newborn Pain and Stress Assessment Scale" is a 3-point Likert-type scale consisting of 5 items, including "facial expression, breathing pattern, tone of extremities, hand/foot activities and activity level" of the newborn, and measurements are made by observation. As the scores obtained increase, pain and stress increase in the newborn. As a result of the evaluation, "3-5 points indicate the presence of mild pain and stress, and more than 5 points indicate the presence of severe pain and stress".
Measured: 9 MONTHS
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2022
- Study start19 Mar 2022
- Primary completion27 Aug 2022
- Study completion19 Dec 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Endotracheal AspirationStudies of the same condition, open and under way.
- More trials run by Ataturk UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Single blind
- Who is masked
- Investigator
- Enrolment
- 88 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ataturk University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, ARZU SARIALİOĞLU, Ataturk University
- Investigators
- ARZU SARIALİOĞLU, PHD, Study director, Ataturk University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05331846
- Sponsor's protocol ID
- B.30.2.ATA.O.oı.OO/l 8
- Status last verified
- Mar 2024
- First submitted
- 10 Apr 2022
- Last updated
- 8 Mar 2024
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: THE ARTICLE IS INTENDED TO BE SHARED AFTER IT IS PUBLISHED
Publications
Deniz B, Sarialioglu A. The Effect of Breast Milk Odor on the Pain and Stress Levels of the Newborn During the Endotracheal Suction Procedure. Breastfeed Med. 2024 Jun;19(6):459-466. doi: 10.1089/bfm.2023.0325. Epub 2024 Mar 25.
PubMed 38526230
Study at a glance
From the registry record, last updated by the sponsor on 8 Mar 2024. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effect of Breast Milk Odor on the Pain and Stress Level of the Newborn During the Endotracheal Aspiration Procedure
- ClinicalTrials.gov ID
- NCT05331846
- Acronym / sponsor ID
- B.30.2.ATA.O.oı.OO/l 8
- Conditions
- Endotracheal Aspiration
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 88 participants (actual)
- Lead sponsor
- Ataturk UniversityUniversity, hospital or other
- Study start
- 19 Mar 2022 (actual)
- Primary completion
- 27 Aug 2022 (actual)
- Study completion
- 19 Dec 2023 (actual)
- First posted
- 18 Apr 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Our study aims to determine the effect of breast milk odor on pain and stress in the application of endotracheal aspiration in newborns hospitalized in the Neonatal Intensive Care Unit. The research is planned experimentally with a pretest posttest randomized control group. The research will be carried out in Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022. The population of the study will consist of patients aged 30-28 days who were hospitalized in the Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022 and received mechanical ventilation treatment.
The research sample; Babies of families who are hospitalized on the dates specified with the probability sampling method and meet the research criteria and volunteer to participate in the research will be formed. Questionnaire Form, Neonatal Pain and Stress Assessment Scale, and Follow-up Form will be used to collect research data. The scent of breast milk will be used as an intervention tool in the research.
Detailed description
3.1. Type of Research The research is planned experimentally with a pretest posttest randomized control group.
3.2. Place and Time of Research The research will be carried out in Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022.
3.3. Population and Sample of the Research The population of the study will consist of patients aged 30-28 days who were hospitalized in the Şanlıurfa Training and Research Hospital Neonatal Intensive Care Unit between March-December 2022 and received mechanical ventilation treatment.
The research sample; Babies of families who are hospitalized on the dates specified with the probability sampling method and meet the research criteria and volunteer to participate in the research will be formed. In this study, a priori power analysis was performed to determine the sample size. In the power analysis, Cohen's standard effect sizes reference method was chosen. In this case, in our study, for the t-test in independent groups in which the effect of sniffed breast milk on endotracheal aspiration application will be compared, it was determined that "80% power at the 95% confidence interval at the 0.05 significance level" could be reached if the study was conducted with a total of 80 participants in two groups with 40 participants in each group. In case of data loss, it was decided to collect data from a total of 88 individuals by including 10% backup sample to this number. Data will be collected at different times from newborns receiving invasive mechanical ventilation support in incubators in the Neonatal Intensive Care Unit. There is no interaction between the groups.
Inclusion Criteria for Research
- Being a term newborn,
- to be between 0-28 days,
- Receiving mechanical ventilation support,
- Not taking opioids or sedatives 4 hours before the procedure. 3.4. Data Collection Tools to be Used in the Research Questionnaire Form, Neonatal Pain and Stress Assessment Scale, and Follow-up Form will be used to collect research data. The scent of breast milk will be used as an intervention tool in the research.
Questionnaire Form: In this form, which was prepared by the researcher by examining the literature; There will be questions about the introductory features of the newborn.
ALPS Neo Neonatal Pain and Stress Rating Scale: The "Newborn Pain and Stress Rating Scale" was developed in 2014, based on the individualized developmental care of the newborn, in order to assess pain and stress in premature and term newborns. In 2017, this scale was adapted to Turkish and validity and reliability studies were conducted. ALPS Neo "Newborn Pain and Stress Assessment Scale" is a 3-point Likert-type scale consisting of 5 items, including "facial expression, breathing pattern, tone of extremities, hand/foot activities and activity level" of the newborn, and measurements are made by observation. As the scores obtained increase, pain and stress increase in the newborn. As a result of the evaluation, "3-5 points indicate the presence of mild pain and stress, and more than 5 points indicate the presence of severe pain and stress".
Follow-up Form: It is the form used to record the cardiorespiratory parameters (peak heart rate, oxygen saturation) of the newborn evaluated before, during and after the procedure, ALPS Neo pain scale, and crying time result.
Intervention Tool Used in Research Breast Milk Scent: Breast milk scent will be used as an intervention tool in the research. In the study, breast milk will be sniffed 5 minutes before endotracheal aspiration with the help of sterile sponge. As a non-pharmacological method, it is expected that the smell of breast milk will reduce the pain and stress felt during endotracheal aspiration in the newborn.
3.5. Data Collection The research data will be obtained from the babies of the parents who agreed to participate in the research after the researcher gave the parents of the patients preliminary information about the research (the purpose of the research, why the research was conducted, the attempt to relieve the neonatal pain with a non-pharmacological method, etc.) and their written consent was obtained.
Before the endotracheal aspiration attempt is made by the researcher to the experimental group, the patient will smell the breast milk scent with the help of a sterile sponge for 5 minutes.
The purpose of making the patient smell the breast milk; It is to reduce the pain level of the procedure to the minimum level by ensuring that the patient calms down. The researcher will have the patient smell breast milk for 5 minutes before the endotracheal aspiration procedure and will evaluate the patient with the "ALPS Neo Neonatal Pain and Stress Rating Scale" before, during and after the procedure. The control group will be routinely performed in the endotracheal aspiration procedure and will be evaluated with the "ALPS Neo Neonatal Pain and Stress Rating Scale" before, during and after the procedure.
3.6. Evaluation of Data The processing and statistical analysis of the collected data will be done with the analysis software called SPSS (Statistical Package for the Social Sciences) for Windows 20.0.
3.7. Ethical Principles of Research In order to carry out the research, official permission will be obtained from the relevant institution with ethical approval from the Ethics Committee. The purpose of the study will be explained to the parents of the babies with the research group criteria, the questions asked will be answered and their verbal and written consent will be obtained. Parents will be informed that the data collected during the research will be processed anonymously, confidentially, and will not be used outside of the study in question, and that they can leave the study whenever they wish. Since the research is based on the use of data obtained from humans, and therefore, due to the necessity of observing personal rights, the relevant ethical principles "Informed Consent", "Volunteerism" and "Protection of Confidentiality" will be followed.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (investigator)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| SMELL OF BREAST MILK | Experimental | Behavioral: the smell of breast milkthe smell of breast milk will reduce pain and stress |
| control | No intervention | –pain and stress will not decrease |
Who may qualify
- Ages
- 1 day to 28 days
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- Being a term newborn,
- to be between 0-28 days,
- Receiving mechanical ventilation support,
- Not taking opioids or sedatives 4 hours before the procedure.
Key exclusion criteria (3 listed)
- not be between 0-28 days,
- Not receiving mechanical ventilation support,
- Taking opioids or sedatives 4 hours before the procedure.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| the smell of breast milkSmell of breast milk during endotracheal aspiration will reduce pain and stress | Behavioural | SMELL OF BREAST MILK |
Primary outcome
ALPS Neo Neonatal Pain and Stress Rating Scale
Time frame: 9 MONTHS
In 2014, the "Newborn Pain and Stress Rating Scale" was developed based on the individualized developmental care of the newborn in order to evaluate pain and stress in premature and term newborns. In 2017, this scale was adapted to Turkish and validity and reliability studies were conducted. ALPS Neo "Newborn Pain and Stress Assessment Scale" is a 3-point Likert-type scale consisting of 5 items, including "facial expression, breathing pattern, tone of extremities, hand/foot activities and activity level" of the newborn, and measurements are made by observation. As the scores obtained increase, pain and stress increase in the newborn. As a result of the evaluation, "3-5 points indicate the presence of mild pain and stress, and more than 5 points indicate the presence of severe pain and stress".
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Mar 2024.
- Derived from this study: PubMed 38526230Deniz B, Sarialioglu A. The Effect of Breast Milk Odor on the Pain and Stress Levels of the Newborn During the Endotracheal Suction Procedure. Breastfeed Med. 2024 Jun;19(6):459-466. doi: 10.1089/bfm.2023.0325. Epub 2024 Mar 25.
- Individual participant dataSharing planned: No. THE ARTICLE IS INTENDED TO BE SHARED AFTER IT IS PUBLISHED
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
ARZU SARIALİOĞLU, PHD study director
Ataturk University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing the smell of breast milk in people with Endotracheal Aspiration, run by Ataturk 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 4 inclusion and 3 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 8 Mar 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?
ALPS Neo Neonatal Pain and Stress Rating Scale (time frame: 9 MONTHS). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05331846, which also lists 1 linked publication.
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 8 Mar 2024.