Clinical Trial

REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Active, Not Recruiting Phase 3
View on ClinicalTrials.gov →
Summary
The purpose of this research study is to learn how two different supportive programs may help women feel better after surgery. This study will measure if one type of supportive program is more useful than the other for improving wellbeing after surgery.
Trial Details
NCT Number NCT05625360
Lead Sponsor Wake Forest University Health Sciences
Collaborators: National Cancer Institute (NCI)
Conditions Postoperative Pain, Acute, Postoperative Depression, Anxiety, Sleep Disturbance, Malignant Female Reproductive System Neoplasm
Enrollment 160 participants
Start Date 2023-06-13
Primary Completion 2026-08-31 (estimated)
Study Completion 2026-08-31 (estimated)
Updated on ClinicalTrials.gov 2026-06-11