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The Impact of Mindfulness Meditation Training on Perinatal Pain for Pregnant Women .

The Impact of Mindfulness Meditation Training on Perinatal Pain for Pregnant Women .

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083661
Enrollment
Unknown
Registered
2024-04-30
Start date
2024-05-01
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Perinatal Pain for Pregnant Women

Interventions

Control group:Listen to Guqin music every day for 30 min
Experimental group:Mindfulness meditation training was performed daily for 30 min

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
24 Years to 35 Years

Inclusion criteria

Inclusion criteria: (1) Pregnant women (28 weeks), aged 24-35 years old; (2) The ASA grade is grade I~II; (3) High school degree or above, able to understand the meaning of the scale; (4) Pregnant women and fetal health, without serious congenital diseases; (5) Willing to accept the cooperation to complete the mindfulness meditation course, and agree to sign the relevant informed consent form.

Exclusion criteria

Exclusion criteria: (1) A history of severe physical illness and mental illness; (2) Pregnant women with hypertension (systolic / diastolic blood pressure over 130 / 90 mmHg) and diabetes mellitus (fasting blood glucose test 5.1 mmol/L or 1 h> 10.0 test in OGTT mmol/L or OGTT test 2 h> 8.5 mmol/L) during pregnancy; (3) Pregnant women with placenta previa or placental abruption during pregnancy; (4) Pregnant women with pregnancy complicated with heart disease; (5) The test pregnant women who cannot understand the content of the relevant scale; (6) The pregnant Women with physiological defects found in the fetus is not suitable for continuing pregnancy; (7) The test pregnant women that the investigator considers has the adverse hazard factors that are not suitable to participate in the trial; (8) Uncontrolled or untreated hypertension patients before pregnancy (arterial hypertension, systolic / diastolic blood pressure over 180 / 100 mmHg at rest); (9) unwilling to cooperate with mindfulness meditation training.

Design outcomes

Primary

MeasureTime frame
Amount of opioid analgesia using intravenous controlled analgesia (PCIA) after cesarean section;Amount of local anesthetic and opioid analgesia in painless delivery;Vital signs (blood pressure, heart rate, blood oxygen saturation, etc.) and pain scores at the incubation period of the first stage of labor, the first stage of labor, the end of labor, the end of the second stage of labor);Fetal condition (Apgar score at 1 min, 5 min and 10 min after delivery);

Secondary

MeasureTime frame
Depression;Mindful Attention Awareness Scale, MAAS;

Countries

China

Contacts

Public ContactWenyuan Wang

Zhejiang Provincial People's Hospital

Neuro-anesth@hotmail.com+86 1358808716

Outcome results

None listed

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