About this trial
Participants may take part in this study if they are scheduled to undergo a surgery that meets the following: (1) traditional open surgery via laparotomy, (2) length of surgery \>3 hours, and (3) curative-intent surgical resection of a cancer in the stomach, pancreas, bile ducts, liver, or peritoneal surfaces. The purpose of this study is (1) to evaluate the feasibility of collecting blood samples prior to surgery, post-surgery and pre- music-assisted relaxation and imagery (MARI) intervention, and immediately post-MARI intervention and (2) to identify gene expression changes associated with MARI and explore their relationship with immediate changes in pain intensity. Participants will be in this study for the duration of their hospital admission for surgery.
Eligibility criteria
Qualifiers
Age 50 to 80
Able to speak and understand English
Scheduled to undergo a surgery meeting the following criteria: (1) traditional open surgery (not laparoscopic or robotic) via laparotomy (midline or subcostal incisions), (2) length of surgery >3 hours, and (3) curative-intent surgical resection of a cancer in the stomach, pancreas, bile ducts, liver, or peritoneal surfaces
Participant reports pain intensity of 4/10 or above to study staff on day 1 post-surgery or any other day post-surgery through discharge
Disqualifiers
Significant visual impairment that has not been corrected
Significant hearing impairment that has not been corrected
Significant cognitive impairment that would prevent participant from participating in the study
Trial design
Treatments tested in this trial
- Music-assisted relaxation and imagery (MARI)
Treatment groups
Locations
1Sponsors and collaborators
Case Comprehensive Cancer Center
Lead sponsor
National Center for Complementary and Integrative Health (NCCIH)
Collaborator