Study of Applying Acupressure in Low-birth Weight Premature
NCT ID: NCT03061968
Last Updated: 2017-02-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2010-05-31
2017-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
SINGLE
Study Groups
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experimental group
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.
acupressure
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.
control group
The control group only receive routine care in sick baby room unite.
No interventions assigned to this group
Interventions
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acupressure
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.
Eligibility Criteria
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Inclusion Criteria
37 Weeks
ALL
No
Sponsors
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China Medical University Hospital
OTHER
Li-Li Chen
OTHER
Responsible Party
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Li-Li Chen
Principal Investigator
Other Identifiers
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DMR98-IRB-245-1
Identifier Type: -
Identifier Source: org_study_id
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