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The early invention on improving survival quality of very low birth weight premature infants

The early invention on improving survival quality of very low birth weight premature infants

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17010454
Enrollment
Unknown
Registered
2017-01-17
Start date
2013-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

neuropsychological abnormality

Interventions

control group:conventional occupational therapy
experimental group: spine and head pinching therapy plus conventional occupational therapy

Sponsors

Fujian Provincial Maternity and Children's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 37 Weeks

Inclusion criteria

Inclusion criteria: 1) gestational age 26–36 and birth weight is from 600 to1,500g; 2) principle guardian of the preterm infant agreed to participate in the research and signed informed consent.

Exclusion criteria

Exclusion criteria: 1) comorbidity of inherited metabolic diseases; 2) grade IV neonatal intraventricular hemorrhage; 3) severe hypoxic-ischemic encephalopathy; 4) history of invasive ventilation treatment; 5) Apgar score at birth <4; 6) mother with diabetic ketoacidosis, severe preeclampsia, severe anemia or acute viral infection during pregnancy.

Design outcomes

Primary

MeasureTime frame
neuropsychological development scale for children aged 0–6 years;incidence of CP;

Secondary

MeasureTime frame
Chinese Infant Toddler Social Emotional Assessment;S-M scales;

Countries

China

Contacts

Public ContactPing OU

Fujian Provincial Maternity and Children's Hospital

eve1019@126.com+86 13905916211

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 25, 2026