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NCT Number: NCT07284303

Infant Swing and Sleep-Wake Cycles

This study was planned to determine the effects of automatic baby swing application on the sleep-wake cycle, comfort behaviors and physiological parameters of babies in the neonatal intensive care unit.

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Key information

Age range

35 week–42 week

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Sleep patterns and behavioral comfort during the neonatal period are important indicators of neurological development and physiological stability. However, noise, light, and constant medical interventions and care practices in the NICU environment can negatively affect infants' sleep continuity and quality of rest. Therefore, non-pharmacological approaches that provide sensory support, such as rhythmic and gentle rocking, are thought to be effective in promoting infant relaxation and physiological balance. In this study, an automatic baby swing with adjustable speed and rhythm will be used as an intervention to support infant comfort and sleep organization. Clinically stable term and preterm newborns who meet the specified inclusion criteria will be included in the study. Participants will be randomly assigned to two groups: the intervention group (first automatic swing application, then measurement without the swing) and the control group (first measurement without the swing, then measurement in the automatic baby swing). The intervention will be implemented for 60 minutes after daytime care at 9:00 AM and 12:00 PM, and for 60 minutes after nighttime care at 9:00 PM and 12:00 AM. The infants' BIS values, comfort, and physiological parameters will be monitored throughout the entire process. The study will evaluate the infants' sleep-wake cycles, comfort behaviors (e.g., facial expressions, body movements, crying), and physiological parameters (e.g., heart rate, respiratory rate, oxygen saturation) as outcome variables. Data will be collected using standardized observation forms and monitoring devices. This study is expected to contribute to evidence-based nursing practice by demonstrating the effects of movement-based nonpharmacological interventions on newborn comfort, sleep quality, and physiological stability.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • gestational age between 35-42 weeks,
  • birth weight >2000-4200 grams,
  • stable health status,
  • spontaneous breathing,
  • no sedation,
  • parental volunteering to participate in the study.

Exclusion criteria

  • - A 5-minute APGAR score below 4 at birth,
  • Requirement of resuscitation,
  • Presence of a congenital anomaly,
  • Requirement of interventional intervention in the head region,
  • Presence of central nervous system dysfunction,
  • Presence of postpartum medical complications.

Exclusion criteria

(during the research):

Sudden need for resuscitation Sudden deterioration of the stabilization of health status

Treatment and study plan

Care: Automatic Baby Swing

Other

The Automatic Baby Swing aims to calm the baby by mimicking their natural movements. In this study, the low-speed "Rock-a-Bye" mode will be used because it mimics natural parental movements, making it easier for babies to fall asleep. During the implementation phase: After the baby's general condition is checked, the treatment will begin according to the group to which they were randomly assigned. If the baby is assigned to the Automatic Baby Swing, their sleep, comfort, and physiological parameters will be measured "First in the Automatic Baby Swing, Then in the Incubator" for 60 minutes during the day and night. If the baby is assigned to the other group, their sleep, comfort, and physiological parameters will be measured "First in the Incubator, Then in the Automatic Baby Swing" for 60 minutes during the day and night.

Primary outcomes

  1. Primary Outcome 1: COMFORTneo Total Score

    Time frame: At 0, 30, and 60 minutes.

    The COMFORTneo scale assesses seven behavioral and physiological parameters (muscle tone, alertness, facial tension, calmness/agitation, body movements, respiratory response, and crying). These parameters will be combined to produce a single total score (range 6-30). Only the total score will be reported.

Secondary outcomes

  1. Secondary Outcome 1: Infant Body Temperature

    Time frame: At 0, 30, and 60 minutes.

    Infant axillary body temperature measured in degrees Celsius (°C).

  2. Secondary Outcome 2: Infant Heart Rate

    Time frame: At 0, 30, and 60 minutes.

    Infant heart rate measured in beats per minute.

  3. Secondary Outcome 3: Infant Respiratory Rate

    Time frame: At 0, 30, and 60 minutes.

    Infant respiratory rate measured in breaths per minute.

  4. Secondary Outcome 4: Infant Oxygen Saturation

    Time frame: At 0, 30, and 60 minutes.

    Pulse oximetry oxygen saturation measured as %SpO₂.

  5. Secondary Outcome 5: Infant Blood Pressure

    Time frame: At 0, 30, and 60 minutes.

    Non-invasive systolic and diastolic blood pressure measured in mmHg.

Study contacts

Contact information is provided by the study sponsor or research team.

Edanur Tar Bolacalı, PhD

CONTACT

[email protected]

+905332668360 ext. +908504412483

Sibel Kucukoglu, PhD

CONTACT

[email protected]

+903322231623

Sponsors and collaborators

Lead sponsor

Kirsehir Ahi Evran Universitesi

Other

Registry information

Official study title

Effect of an Automatic Infant Swing on Sleep-Wake Cycles, Comfort Behaviors, and Physiological Parameters in Newborns: A Randomized Controlled Trial

Acronym: AISS

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 16, 2025
Registry last updated
Dec 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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