NCT07090018
Empowered Relief: A One-Time Session to Help Postpartum Women Manage Ongoing Pain After Cesarean Delivery
Enrolling by Invitation
NAAges 18+InterventionalTreatmentStanford UniversityInvestigator-initiated
~60 participants
Updated 2025-11-20 on ClinicalTrials.gov
What's tested:Empowered Relief
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of participants registering for Empowered Relief session
Measured over Baseline (up to 1 week)
+3 more outcomes measured
Conditions
Where it's being run
1 sites across 1 statesCalifornia1
Study leadership
- Pervez Sultan, MBChB, FRCA, MD(Res) · PRINCIPAL_INVESTIGATOR · Stanford University
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Eligibility criteria
Inclusion
Females 18 years of age or older
Any postpartum woman who has had a cesarean delivery in the Stanford Healthcare system with a viable birth
has moderate/severe pain, scoring ≥ 4/10 on the numerical/visual analog scale that continues at 6 weeks postpartum
English fluency
Ability to adhere to and complete study protocols
Access to smart device for zoom / video meetings
Exclusion
\<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.
What this trial measures
- Percentage of participants registering for Empowered Relief sessionBaseline (up to 1 week)
- Percentage of participants attending Empowered Relief sessionTreatment (up to 2 weeks)
- Participant Satisfaction Scale Score1 - 2 weeks Post treatment
Participant satisfaction will be measured using a 7 item questionnaire (scale ranges from 0 - 42, higher ratings represent greater satisfaction with the treatment).
- Participant Treatment Skills Use Scale Score4 - 6 weeks Post Treatment
Participant treatment skills use will be measured with a 5 items questionnaire (scale ranges from 0 - 25, higher ratings represent increased time using treatment).