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…
- In order to be eligible to participate in this study, an individual must meet all of the following criteria:
- Provision of signed and dated informed consent form
- Participants age 18 years and older at time of consent.
- Scheduled for an abdominal gynecological surgery (i.e., uterine, ovarian) to remove a mass that is suspected to be malignant
- Have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1
- Able to understand, read and write English (since the intervention is conducted in English)
You may not qualify if…
- An individual who meets any of the following criteria will be excluded from participation in this study:
- Presence of a psychotic disorder, current suicidal ideation, or other unstable major psychiatric condition documented by diagnosis in the medical chart.
- Unwillingness or inability to follow study procedures
Where it is running
- Atrium Health - Levine Cancer Institute — Charlotte, North Carolina, United States
- Wake Forest Baptist Comprehensive Cancer Center — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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