CompletedNot applicableNCT01593657
Official study title

Mindful Movement and Breathing to Improve Outcomes of Gynecologic Surgery

Study summary

The purpose of this clinical trial is to understand if women undergoing surgery for a suspected gynecologic malignancy are interested in participating in a Mindful Movement and Breathing program and what the effects of this program are on women and the surgery-related symptoms they experience. Mindful Movement and Breathing programs may be effective for easing distress, post-surgical pain, and other symptoms of surgical procedures.

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Key things to know

Main goalSupportive Care

This describes the study’s primary purpose.

What is being studiedMindful Movement and Breathing program and Questionnaire administration

Plus 2 other study approaches.

Who it may be forGynecologic Malignancy · Abdominal Surgery by Laparotomy

These are broad labels—not an eligibility decision.

Checked against the public recordLast updated Jul 3, 2018 · Source: ClinicalTrials.gov

Is enrollment open?Completed

Ask the study team to confirm whether enrollment is open.

What kind of study?Not applicable

Interventional

Where is it offered?1 U.S. location

Locations may change over time.

Who runs it?Wake Forest University Health Sciences

Study sponsor

01
Study overview

What this study is about

Purpose
Supportive Care
Study type
Interventional
Phase
Not applicable
Sponsor
Wake Forest University Health Sciences
Interventions being studied
Other: Mindful Movement and Breathing program; Other: Questionnaire administration; Procedure: The Observer Mobility Scale; Procedure: Volumetric Incentive Spirometry
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
03
Public criteria

Who may be able to participate

The sponsor separates these requirements into two groups. You do not need to interpret them alone—use them to guide a conversation with the study team.

Requirements people may need to meetInclusion criteria
  • Signed protocol specific informed consent
  • 18 years of age or older
  • Scheduled for a major abdominal gynecological surgery to remove a mass that is suspected to be malignant
Reasons someone may not be able to joinExclusion criteria
  • Unable to read or understand English
  • Cognitively impaired and/or cannot complete interviews as judged by the referring physician, nurse, or study staff

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Wake Forest University Health SciencesWinston-Salem, North Carolina

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Jul 3, 2018. Always confirm current availability with the study team.

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