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NCT05625360 | RECRUITING | Postoperative Pain, Acute


REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss
Sponsor:

Wake Forest University Health Sciences

Brief 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.

Condition or disease

Postoperative Pain, Acute

Postoperative Depression

Anxiety

Sleep Disturbance

Malignant Female Reproductive System Neoplasm

Intervention/treatment

eHealth Mindful Movement and Breathing

Life Impacts Reflection

PROMIS Questionnaires

Phase

PHASE3

Detailed Description:

Primary Objective: To determine efficacy of eHealth Mindful Movement and Breathing (eMMB) as compared to Life Impact Reflection (LIR) for improving postoperative pain intensity 4-weeks postoperative in patients who received abdominal surgery for a suspected gynecologic malignancy. Secondary Objectives: * At week 2 and 3 months post-operative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving pain intensity in patients who received abdominal surgery for a suspected gynecologic malignancy. * At week 2, week 4, and 3 months postoperative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving affective pain in patients who received abdominal surgery for a suspected gynecologic malignancy. * To determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving post-operative acute pain (pain intensity within 1 week post-surgery) in patients who received abdominal surgery for a suspected gynecologic malignancy. * At week 2, week 4, and 3 months postoperative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving pain interference in patients who received abdominal surgery for a suspected gynecologic malignancy. * At week 2, week 4, and 3 months postoperative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving psychological distress symptoms (i.e., depression) in patients who received abdominal surgery for a suspected gynecologic malignancy. * At week 2, week 4, and 3 months postoperative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving psychological distress symptoms (i.e., anxiety) in patients who received abdominal surgery for a suspected gynecologic malignancy. * At week 2, week 4, and 3 months postoperative, to determine efficacy of eHealth Mindful Movement and Breathing as compared to LIR for improving sleep disturbances in patients who received abdominal surgery for a suspected gynecologic malignancy.

Study Type : INTERVENTIONAL
Estimated Enrollment : 160 participants
Masking : QUADRUPLE
Primary Purpose : SUPPORTIVE_CARE
Official Title : REmotely-delivered Supportive Programs for Improving Surgical Pain Dnd disTrEss (RESPITE)
Actual Study Start Date : 2023-06-13
Estimated Primary Completion Date : 2026-08-31
Estimated Study Completion Date : 2026-08-31

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: FEMALE
Accepts Healthy Volunteers: 1
Criteria
Inclusion Criteria
  • 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
    • * 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)
    Exclusion Criteria
    • 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

REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Location Details

NCT05625360


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How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations


RECRUITING

United States, North Carolina

Atrium Health - Levine Cancer Institute

Charlotte, North Carolina, United States, 28204

RECRUITING

United States, North Carolina

Wake Forest Baptist Comprehensive Cancer Center

Winston-Salem, North Carolina, United States, 27157

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