RECRUITING

REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2023-06-13
Study Completion:2026-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05625360

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Provision of signed and dated informed consent form
  2. * Participants age 18 years and older
  3. * Scheduled for an abdominal gynecological surgery (i.e., uterine, ovarian) to remove a mass that is suspected to be malignant
  4. * Have an Eastern Cooperative Oncology Group (ECOG) performance status of ≤1
  5. * Able to understand, read and write English (since the intervention is conducted in English)
  1. * Presence of a psychotic disorder, current suicidal ideation, or other unstable major psychiatric condition documented by diagnosis in the medical chart.
  2. * Unwillingness or inability to follow study procedures

Contacts and Locations

Study Contact

Hannah O'Brien
CONTACT
336-716-2498
hobrien@wakehealth.edu
Alicia Patrick, MA, CCRP
CONTACT
980-292-1746

Principal Investigator

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

Study Locations (Sites)

Atrium Health - Levine Cancer Institute
Charlotte, North Carolina, 28204
United States
Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, 27157
United States

Collaborators and Investigators

Sponsor: Wake Forest University Health Sciences

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

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-13
Study Completion Date2026-08-31

Study Record Updates

Study Start Date2023-06-13
Study Completion Date2026-08-31

Terms related to this study

Additional Relevant MeSH Terms

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