Reducing Chronic Pain Following Cesarean Delivery

NCT ID
NCT07799883
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Stanford University
Conditions
Cesarean Section Complications, Chronic Pain, Postpartum

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: A Pilot Feasibility Study of an Intervention to Reduce Chronic Pain Following Cesarean Delivery

Enrollment: 30 participants (Estimated).

What is being studied

  • Behavioral: Empowered Relief

Who may be eligible

Ages
18 Years to no maximum
Sex
Female
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Complete informed consent. 2. Age 18 years or above. 3. Postpartum woman who delivered by cesarean within the Stanford Healthcare system. 4. Viable birth (singleton or multiple gestation). 5. All maternal demographics and complications are eligible: parity, medical conditions (e.g., pre-eclampsia, gestational diabetes), and post-surgical complications (e.g., hysterectomy, ICU admission, extended hospital stay). 6. All neonatal complications are eligible (e.g., NICU admission, extended hospital stay) 7. Attend the 6-week postpartum clinic visit. 8. Any pain intensity (numeric rating scale \[NRS\] \>0/10) and/or pain interference (PROMIS pain interference 8a score \>8) at 6 weeks postpartum. 9. English fluency, with ability to read and write. 10. Ability to adhere to and complete study procedures. 11. Access to a smart device if attending ER session via Zoom. Exclusion Criteria: 1. Age under 18 years. 2. Cognitive impairment or psychological factors that would preclude comprehension of study material or full participation. 3. Unable or unwilling to provide informed consent. 4. Chronic pain prior to pregnancy.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: United States

  • California, United States: 1

Sample of listed locations

  • Stanford Medicine Children's Health - Specialty Services, Welch Road — Palo Alto, California, 94304, United States — Site recruitment status not specified in the registry data

Study details

Start date
October 5, 2026
Primary completion date
January 31, 2027
Completion date
March 14, 2027
First posted
September 2, 2026
Collaborators
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institute on Drug Abuse (NIDA)

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07799883
Registry last updated
September 28, 2026
QualifiedStudies registry data refreshed
October 2, 2026
QualifiedStudies record fetched
October 2, 2026

View NCT07799883 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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