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ENROLLING_BY_INVITATIONNA

Using Empowered Relief and Education To Help Postpartum Women Recover After Cesarean Delivery

A Pilot Feasibility Trial for a Comprehensive Multimodal Intervention to Assess Global Recovery Following Cesarean Delivery

NCT07192718•Stanford University

View on ClinicalTrials.gov

Summary

The purpose of this study is to study the effect of a pain relief skills session (Empowered Relief) and educational content on global postpartum recovery at 12 weeks post cesarean delivery.

Eligibility

Age

18 - No limit years

Sex

FEMALE

Healthy Volunteers

Inclusion Criteria

•Females 18 years of age or older
•Any woman scheduled for a cesarean delivery in the Stanford Healthcare system with a viable birth
•English fluency
•Ability to adhere to and complete study protocols
•Access to smart device for zoom / video meetings

Exclusion Criteria

•\<18yrs
•chronic pain prior to pregnancy
•Cognitive impairment, non-English speaking, or psychological factors that would preclude comprehension of material and/or full participation in the study.

Locations (1)

Stanford University

Palo Alto, California, United States

Key Dates

Start Date

December 2, 2025

Primary Completion Date

December 1, 2026

Completion Date

December 1, 2026

Last Updated

March 10, 2026

Enrollment

ESTIMATED participants

Conditions

Cesarean Section ComplicationsPostpartum Care

Interventions

Empowered Relief

BEHAVIORAL

Education

OTHER

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RECRUITINGNA

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: March 10, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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Using Empowered Relief and Education To Help Postpartum Women Recover After Cesarean Delivery

Inclusion Criteria

Exclusion Criteria

Effectiveness Study of a Lifestyle Intervention Versus Metformin in Mothers With Recent Gestational Diabetes

Management of Prelabor Rupture of the Membranes at Term

Effects of Intrathecal Midazolam (1mg) With Hyperbaric Bupivacaine 0.5% (15mg) for Spinal Anesthesia for C-section

A Two-Layered Simple Interrupted Myometrial Suturing Reduces Uterine Niche Formation After Primary Cesarean Section

Postplacental Copper Intrauterine Device Versus Postpartum Progesterone-only Pills on Uterine Niche Formation

Evaluation of an mHealth-CHW Tool for Post-c-section Follow-up in Rural Rwanda