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The effect of sound intervention combined with postural intervention on sleep in preterm infants: A randomized controlled trial

The effect of sound intervention combined with postural intervention on sleep in preterm infants: A randomized controlled trial

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064077
Enrollment
Unknown
Registered
2022-09-26
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature infant

Interventions

Control group:We provide routine neonatal care, i.e. developmental support care for preterm infants, including "bird's nest" care and basic care.
Experimental group (Group A):On the basis of routine care, white noise combined with Lullaby were played for 20 min each time, at 10am, 12am and 3pm,respectively.
Experimental group (Group B):Experimental group (Group B): On the basis of routine care, white noise combined with Lullaby were played for 20 min each time, at 10pm, 12pm and 3am,respectively.
Experimental group (Group C):Experimental group (Group C): On the basis of routine care, white noise combined with Lullaby were played for 20 min each time, at 10am, 12am,3pm,10pm,12pmand 3am,respecti

Sponsors

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (a) Gestational age 32-37w; (b) Apgar score >5 at 1 minute after birth.

Exclusion criteria

Exclusion criteria: (a) Preterm infants who failed the hearing screening; (b) Those who had brain disease, intracranial hemorrhage of grade III and above, central nervous system disease, genetic metabolic disease and congenital heart disease; (c) Those who are sedated or mechanically ventilated; (d) Those whose condition deteriorated, abandoned treatment, or died during the study period; (e) Surgical procedures during the study period.

Design outcomes

Primary

MeasureTime frame
duration;

Secondary

MeasureTime frame
efficiency;

Countries

China

Contacts

Public ContactZHU ZHI YU
zhuzhiyu@scmc.com.cn18917861157

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026