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Study on the effect of early comprehensive intervention of skin contact combined with breastfeeding on improving blood glucose in early birth of newborns with gestational diabetes mellitus

Study on the effect of early comprehensive intervention of skin contact combined with breastfeeding on improving blood glucose in early birth of newborns with gestational diabetes mellitus

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059454
Enrollment
Unknown
Registered
2022-04-30
Start date
2021-01-01
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Early neonatal blood glucose

Interventions

Control group:No intervention
Experimental group:Early skin contact

Sponsors

Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 44 Years

Inclusion criteria

Inclusion criteria: 1. Newborns with one foot and full-term GDM (GDM); 2. Pregnant women over the age of 18-44 years; 3. Normal uterine development, good health, single pregnancy; 4. No serious complications and complications during pregnancy, such as severe hypertension, thyroid, liver and kidney diseases requiring drug treatment; 5. Postpartum blood sugar 2.2-7.0 mmol/L; 6. The amount of breast milk >= (+) within 2 hours after delivery can carry out effective breastfeeding; 7. Pregnant women have complete information; 8. Periodic inspection; 9. Informed consent to this study, willing to accept regular follow-up.

Exclusion criteria

Exclusion criteria: 1. Pregnant women with cognitive impairment or abnormal behavior; 2. There is no valid contact information; 3. Prolong the first and second stages of labor; 4. Cesarean section; 5. Maternal fatigue; 6. The condition of the nipple is not good, and the newborn cannot suck effectively; 7. Moderate to severe neonatal asphyxia; 8. Severe birth injury; 9. Those who were asked to withdraw from the study or refused to provide relevant information due to various reasons, and did not give birth in our hospital; 10. Participated in other clinical research during the investigation period; 11. During the intervention period, the puerpera refused to continue to complete the observation indicators.

Design outcomes

Primary

MeasureTime frame
Blood sugar;

Secondary

MeasureTime frame
Neonatal hospitalization rate;Ear temperature;crying;Incidence of postpartum hemorrhage;

Countries

China

Contacts

Public ContactLing Xiang

Wuxi People's Hospital of Jiangsu Province

156708922@qq.com+86 13961706255

Outcome results

None listed

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