REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Description

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.

Conditions

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

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Study Overview

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Study Details

Study overview

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.

REmotely-delivered Supportive Programs for Improving Surgical Pain Dnd disTrEss (RESPITE)

REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Condition
Postoperative Pain, Acute
Intervention / Treatment

-

Contacts and Locations

Charlotte

Atrium Health - Levine Cancer Institute, Charlotte, North Carolina, United States, 28204

Winston-Salem

Wake Forest Baptist Comprehensive Cancer Center, Winston-Salem, North Carolina, United States, 27157

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Provision of signed and dated informed consent form
  • * Participants age 18 years and older
  • * 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)
  • * 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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

Wake Forest University Health Sciences,

Stephanie J Sohl, PhD, PRINCIPAL_INVESTIGATOR, Wake Forest Baptist Comprehensive Cancer Center

Study Record Dates

2026-08-31