Maternal Voice Versus White Noise in Pediatric Surgery
22 sierpnia 2026 zaktualizowane przez: Sinem Öztürkler, Kocaeli University
Maternal Voice Versus White Noise: Effects on Pain, Comfort, and Physiological Responses in Pediatric Surgery
This randomized controlled study will evaluate the effects of maternal voice and white noise on postoperative pain, comfort, and physiological parameters in children aged 1 month to 3 years during the early postoperative period.
The study will also compare the effectiveness of maternal voice and white noise in improving these outcomes.
Przegląd badań
Status
Zakończony
Interwencja / Leczenie
Szczegółowy opis
For the maternal voice intervention, the mother will select a lullaby, and its lyrics will be provided to her by the researcher. The lullaby will be recorded in the mother's voice with the assistance of the researcher. The sound level of the recording will be adjusted to approximately 50 decibels. Children assigned to the maternal voice group will listen to the recorded lullaby during the early postoperative period. A copy of the recording will be provided to the mother after completion of the study.
Children assigned to the white noise group will listen to the white noise recording "Don't Let Your Baby Cry 2" from the album "Colic." The recording includes intrauterine-like and white-noise sounds combined with music. The recording will be used after obtaining the necessary permissions from the relevant copyright holders.
Typ studiów
Interwencyjne
Zapisy (Rzeczywisty)
90
Faza
- Nie dotyczy
Kontakty i lokalizacje
Ta sekcja zawiera dane kontaktowe osób prowadzących badanie oraz informacje o tym, gdzie badanie jest przeprowadzane.
Lokalizacje studiów
-
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İ̇zmi̇t
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Kocaeli, İ̇zmi̇t, Turcja (Türkiye)
- Kocaeli University
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Kryteria uczestnictwa
Badacze szukają osób, które pasują do określonego opisu, zwanego kryteriami kwalifikacyjnymi. Niektóre przykłady tych kryteriów to ogólny stan zdrowia danej osoby lub wcześniejsze leczenie.
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dziecko
Akceptuje zdrowych ochotników
Nie
Opis
Inclusion Criteria:
- Aged 1 to 3 years
- Scheduled to undergo an elective minor surgical procedure, such as orchiopexy, hypospadias repair, or hernia repair
- Undergoing surgery under general anesthesia with an anesthesia duration not exceeding 60 minutes
- No known hearing impairment
- No anatomical abnormality of the ear
- No chronic condition that could affect auditory perception or pain response, such as cerebral palsy, Down syndrome, or another neurodevelopmental disorder
- Scheduled for direct transfer to the pediatric surgery ward after surgery without an extended stay in the postanesthesia care unit
- Written informed consent provided by a parent or legal guardian
Exclusion Criteria:
- Surgery performed under emergency conditions
- A surgical procedure different from the planned procedure
- Anesthesia duration exceeding 60 minutes
- Development of a postoperative complication requiring admission to the postanesthesia care unit or intensive care unit
- Administration of additional analgesic medication beyond the institutional analgesia protocol
- Interruption or inability to complete the 60-minute auditory intervention or observation period
- Withdrawal of consent by the parent or legal guardian
Plan studiów
Ta sekcja zawiera szczegółowe informacje na temat planu badania, w tym sposób zaprojektowania badania i jego pomiary.
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Inny
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Podwójnie
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: Maternal voice
Children received routine postoperative nursing care and listened continuously for 60 minutes to a preoperatively recorded lullaby sung by their mother.
Playback began after baseline physiological measurements following admission to the pediatric surgery ward.
The recording was played through a portable speaker positioned at the head of the child's bed at ear level, with the sound intensity maintained at 50-55 decibels.
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Before surgery, each mother selected and recorded a lullaby in a quiet room with guidance from the researcher.
Following postoperative admission to the pediatric surgery ward, the recording was played continuously to the child for 60 minutes through a portable speaker.
Sound intensity was monitored using a calibrated sound-level meter and maintained at 50-55 decibels.
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Eksperymentalny: White noise
Children received routine postoperative nursing care and listened continuously to a standardized white noise recording for 60 minutes.
Playback began after baseline physiological measurements following admission to the pediatric surgery ward.
The recording was played through a portable speaker positioned at the head of the child's bed at ear level, with the sound intensity maintained at 50-55 decibels.
|
Children listened to the standardized recording "Don't Let Your Baby Cry 2" from the album "Colic."
The recording included intrauterine-like sounds, white-noise frequency components, and accompanying music.
It was played continuously for 60 minutes through a portable speaker.
Sound intensity was monitored using a calibrated sound-level meter and maintained at 50-55 decibels.
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Brak interwencji: Control Arm
Children received routine postoperative nursing care without a structured auditory intervention.
No planned silence or sound restriction was imposed, and the children remained in the usual auditory environment of the pediatric surgery ward.
Outcome assessments were conducted at the same time points as in the intervention groups.
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Postoperative Pain Assessed Using the Face, Legs, Activity, Cry, and Consolability Scale
Ramy czasowe: 30 and 60 minutes after admission to the pediatric surgery ward
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Postoperative pain was assessed using the Face, Legs, Activity, Cry, and Consolability Scale.
The scale evaluates five behavioral domains: facial expression, leg movement, activity, crying, and consolability.
Each domain is scored from 0 to 2, producing a total score ranging from 0 to 10. Higher scores indicate greater postoperative pain and therefore a worse outcome.
The scale was administered at 30 and 60 minutes.
The prespecified primary endpoint was the total score at 60 minutes.
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30 and 60 minutes after admission to the pediatric surgery ward
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Postoperative Recovery Assessed Using the Modified Aldrete Recovery Score
Ramy czasowe: 30 and 60 minutes after admission to the pediatric surgery ward
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Postoperative recovery was assessed using the Modified Aldrete Recovery Score.
The scale evaluates five domains: motor activity, respiration, circulation, consciousness, and peripheral oxygen saturation.
Each domain is scored from 0 to 2, producing a total score ranging from 0 to 10. Higher scores indicate a better level of postoperative recovery.
A score of 9 or higher generally indicates readiness for discharge from postanesthesia care.
The scale was administered at 30 and 60 minutes.
The prespecified secondary endpoint was the total score at 60 minutes.
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30 and 60 minutes after admission to the pediatric surgery ward
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Heart Rate
Ramy czasowe: Immediately after admission and before the intervention, and at 30 and 60 minutes
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Heart rate was measured using a pulse oximeter and recorded as beats per minute.
Lower values within the age-appropriate physiological range indicate reduced physiological arousal; however, the measure does not have a predefined better or worse direction independently of the clinical context.
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Immediately after admission and before the intervention, and at 30 and 60 minutes
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Respiratory Rate
Ramy czasowe: Immediately after admission and before the intervention, and at 30 and 60 minutes
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Respiratory rate was recorded as breaths per minute.
Lower values within the age-appropriate physiological range may indicate reduced physiological arousal; however, the measure does not have a predefined better or worse direction independently of the clinical context.
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Immediately after admission and before the intervention, and at 30 and 60 minutes
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Peripheral Oxygen Saturation
Ramy czasowe: Immediately after admission and before the intervention, and at 30 and 60 minutes
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Peripheral oxygen saturation was measured using a pulse oximeter and recorded as a percentage.
Higher values within the clinically expected range indicate better oxygenation.
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Immediately after admission and before the intervention, and at 30 and 60 minutes
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Współpracownicy i badacze
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Sponsor
Daty zapisu na studia
Daty te śledzą postęp w przesyłaniu rekordów badań i podsumowań wyników do ClinicalTrials.gov. Zapisy badań i zgłoszone wyniki są przeglądane przez National Library of Medicine (NLM), aby upewnić się, że spełniają określone standardy kontroli jakości, zanim zostaną opublikowane na publicznej stronie internetowej.
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
1 stycznia 2024
Zakończenie podstawowe (Rzeczywisty)
1 stycznia 2025
Ukończenie studiów (Rzeczywisty)
1 stycznia 2026
Daty rejestracji na studia
Pierwszy przesłany
16 czerwca 2026
Pierwszy przesłany, który spełnia kryteria kontroli jakości
22 sierpnia 2026
Pierwszy wysłany (Rzeczywisty)
25 sierpnia 2026
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
25 sierpnia 2026
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
22 sierpnia 2026
Ostatnia weryfikacja
1 sierpnia 2026
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 2023/361
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
NIE
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Nie
Bada produkt urządzenia regulowany przez amerykańską FDA
Nie
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