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Study of Applying Acupressure in Low-birth Weight Premature

L

Li-Li Chen

Status

Unknown

Conditions

Premature

Treatments

Behavioral: acupressure

Study type

Interventional

Funder types

Other

Identifiers

NCT03061968
DMR98-IRB-245-1

Details and patient eligibility

About

The purpose of this study is to investigate the effects of acupressure application in very low birth weight premature.

Full description

A quasi-experimental study is designed. Sixty premature babies will be recruited by purposed sampling, according to the criteria of very low birth weight (<1500gm) from a sick baby room in a medical center. The control group only receive routine care in sick baby room unite. The babies in experimental group will be observed for one day, and then intervene the simplified acupressure three times a day for 15 days, and continuously recoding the observation and records until discharge. The intervention includes acupressure for 15 minutes each at 10Am, 1Pm and 4Pm.

Enrollment

60 estimated patients

Sex

All

Ages

Under 37 weeks old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • according to the criteria of very low birth weight (<1500gm) from a sick baby room in a medical center.

Exclusion criteria

  • Exclusion criteria of very low birth weight (>1500gm) from a sick baby room in a medical center.

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 2 patient groups

experimental group
Experimental group
Description:
The babies in experimental group will be observed for one day, and then intervene the simplified acupressure three times a day for fifteen days, and continuously recoding the observation and records until discharge.
Treatment:
Behavioral: acupressure
control group
No Intervention group
Description:
The control group only receive routine care in sick baby room unite.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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