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A randomised controlled study of the effects of personalised exercise intervention on glycemic control and perinatal outcomes in pregnant women with gestational diabetes

A randomised controlled study of the effects of personalised exercise intervention on glycemic control and perinatal outcomes in pregnant women with gestational diabetes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106385
Enrollment
Unknown
Registered
2025-07-23
Start date
2025-07-02
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Gestational diabetes mellitus

Interventions

Control group A:Participated in routine health education during pregnancy and did not receive exercise intervention.
Control group B:On the basis of routine nursing and health education in control group A, routine standardized exercise intervention (5 days a week, 30 minutes of moderate-intensity exercise each time)
Intervention group::Based on the usual nursing and health education of the control group A, exercise intervention was carried out according to the personalized physical activity predicted by the model

Sponsors

Women's Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Pregnant women who plan to have regular obstetric checkups and deliver in their experimental hospitals; 2.Pregnant women diagnosed with GDM; 3. 24 weeks-28 weeks of gestation; 4. Singleton pregnancies; 5. Complete clinical data; 6. Obtaining the consent of the individual and signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Assisted reproductive technology; 2. Those with a history of hepatitis series disease, severe hematologic disease, malignant neoplasm, combined vital organ dysfunction, or severe systemic underlying disease; 3. Termination of pregnancy during follow-up; 4. Pregnant women receiving insulin or oral hypoglycemic agents; 5. Those suffering from pregnancy-related comorbidities; 6. Those with contraindications to exercise; 7. Patients who are participating in other clinical studies; 8. Those with cognitive dysfunction mental illness or communication disorders; 9. Those with diabetes mellitus prior to pregnancy; 10. Those who, in the opinion of the investigator, are otherwise unsuitable for clinical research.

Design outcomes

Primary

MeasureTime frame
Physical activity;Blood glucose;

Secondary

MeasureTime frame
Perinatal outcome;

Countries

China

Contacts

Public ContactDanqing Chen

Women's Hospital, School of Medicine, Zhejiang University

xiaoxiao000719@163.com+86 136 0664 6789

Outcome results

None listed

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