RecruitingNot ApplicableNCT06949943

Pre-Operative Guided Meditation to Reduce Pre-Operative Anxiety in Patients Undergoing Cancer-Directed Surgery

Enhancing Quality of Patient Experience Via an Innovative Reduction of Pre-Operative Anxiety


Sponsor

Ohio State University Comprehensive Cancer Center

Enrollment

200 participants

Start Date

Mar 14, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This clinical trial tests how well guided meditation, compared to silence, works to reduce pre-operative anxiety in patients undergoing cancer-directed surgery. Pre-operative anxiety affects patient experience and has been found to be a predictor of severe post-operative pain and chronic pain after surgery, influencing the success and quality of a patient's recovery. While medication is often prescribed to improve anxiety symptoms, research has showed that mindfulness techniques can be used to decrease anxiety, improve comfort, and can impact both psychological and physiologic symptoms. Completing pre-operative guided meditation may work well to reduce pre-operative anxiety in patients undergoing cancer directive surgery.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Participants will be recruited among patients who are scheduled for cancer-directed surgery
  • Participants must be 18 years or older

Exclusion Criteria5

  • Participants will be excluded from the study if they cannot speak English (as the meditation is recorded in English)
  • Currently incarcerated
  • Have a diagnosis of dementia
  • Are admitted to the intensive care unit (ICU)
  • Have a hearing impairment that would make them unable to hear the recorded meditation

Interventions

BEHAVIORALBehavioral Intervention

Listen to guided meditation

BEHAVIORALBehavioral Intervention

Wear noise cancelling headphones

OTHERElectronic Health Record Review

Ancillary studies

OTHERSurvey Administration

Ancillary studies


Locations(1)

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

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NCT06949943


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