REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Running, not enrolling · Phase 3

Conditions studied: Postoperative Pain, Acute, Postoperative Depression, Anxiety, Sleep Disturbance, Malignant Female Reproductive System Neoplasm

In brief

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.

Key facts

Study ID
NCT05625360
Run by
Wake Forest University Health Sciences
People needed
160
Starts
2023-06-13
Expected to finish
2026-10-31
Last updated by the study team
2026-07-24

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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