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Study on the dose-dependent relationship and possible mechanism between exercise during pregnancy and perinatal depression symptoms

Study on the dose-dependent relationship and possible mechanism between exercise during pregnancy and perinatal depression symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400090117
Enrollment
Unknown
Registered
2024-09-24
Start date
2024-09-27
Completion date
Unknown
Last updated
2024-09-30

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

Conditions

Perinatal depression

Interventions

Preoperative Regular Exercise Group:None
Preoperative irregular exercise group:none

Sponsors

Anhui Wanbei Coal-Electricity Group General Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) 18-45 year old young female; (2) ASA Level I-II; (3) BMI 18.5--25kg/m2; (4) Planned cesarean section surgery.

Exclusion criteria

Exclusion criteria: (1) Having prenatal mental disorders, including depression and communication difficulties; (2) There are contraindications to spinal anesthesia or switching to other anesthesia regimens during surgery; (3) Patients with severe pregnancy complications such as placenta accreta or HELLP syndrome (intravascular hemolysis, elevated liver enzymes, and low platelet count), preeclampsia, eclampsia, placenta previa, placental abruption, and placental hyperplasia; (4) Patients with significant intraoperative bleeding, severe arrhythmia, or sudden events; (5) ASA = III, severe cardiovascular disease, requiring emergency surgery again after surgery; (6) Patients who are unable or unwilling to cooperate with questionnaire surveys and clinical examinations are also excluded.

Design outcomes

Primary

MeasureTime frame
Hospital Anxiety Depression Scale Scores;Edinburgh Postnatal Depression Scale scores;

Secondary

MeasureTime frame
Numeric Rating Scale Pain Score;Depression-related factors in blood and cerebrospinal fluid;Imaging (e.g., MRI) related testing status;Incidence of nausea, vomiting and other adverse reactions;

Countries

China

Contacts

Public ContactChen Haitao

Anhui Wanbei Coal-Electricity Group General Hospital

36854693@qq.com+86 138 5578 0665

Outcome results

None listed

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