Prospective cohort study on postpartum pain and recovery after vaginal delivery with and without labor analgesia.

Prospective cohort study on postpartum pain and recovery after vaginal delivery with and without labor analgesia. - Prospective study on postpartum pain and recovery.

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000039343

Enrollment

300

Registered

2020-01-31

Start date

2020-01-31

Completion date

Unknown

Last updated

2026-06-29

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

Conditions

Post vaginal delivery

Interventions

None listed

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: Women who are: - planning to have vaginal delivery at St Luke's International Hospital before 11/24/2020. - able to read, write and have conversation in Japanese - equal to or above 20 years old - primipara - 35 weeks gestation or later - without serious maternal or fetal complications

Exclusion criteria

Exclusion criteria: - maternal complications: chronic or pregnancy-induced hypertension requiring medical interventions, active psychiatric disorders (including depression, anxiety disorder), diabetes requiring medical intervention, non-singleton pregnancy, chronic pain or chronic opioid use. - allergy to materials used in the activity tracker (fitbit)

Design outcomes

Primary

Measure	Time frame
Postpartum pain score on numeric rating scale.	—

Countries

Japan

Contacts

Public ContactAyumi Maeda

Brigham and Women's Hospital Department of Anesthesiology, Perioperative and Pain Medicine

amaeda@bwh.harvard.edu1-617-732-5500

Outcome results