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Recruiting
NCT07618559
The Food Network Effect
Conditions: Post Operative Patients
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 150
Sponsor: Casey Morehouse, DO
Location: Prisma Health Midlands Columbia South Carolina
Summary
The goal of this clinical trial is to learn if exposure to food related visual stimuli during the postoperative period can improve gastrointestinal recovery after abdominal surgery in adult patients.The main questions it aims to answer are:
1. Does structured exposure to food related television programming shorten the time to return of bowel function after surgery?
2. Does exposure to food related visual stimuli reduce postoperative ileus and improve recovery related outcomes such as hospital length of stay, appetite, patient satisfaction, and medication use?
Researchers will compare patients receiving structured food related programming during meal periods with patients receiving standard postoperative care to see if food related visual stimulation improves postoperative gastrointestinal recovery.
Participants will:
* Be randomly assigned to either a food-programming group or a standard care group
* Watch food-related television programming for at least 15 minutes during scheduled meal-time periods if assigned to the intervention group
* Have daily collection of routine postoperative information, including bowel function, medication use, and diet progression
* Complete brief optional questions regarding appetite and satisfaction during hospitalization
Eligibility Criteria
Inclusion Criteria:
* Adult patients aged ≥18 years
* Undergoing abdominal surgery (including general, colorectal, trauma, or surgical oncology procedures) requiring inpatient post operative admission
* Able to participate in the intervention, including engaging with television based stimuli
* Able to follow simple instructions in the postoperative period
Exclusion Criteria:
* Critical illness requiring ICU-level care beyond the immediate postoperative period
* Mechanical ventilation (intubated patients)
* Requirement for high-level non-invasive ventilation (BiPAP for respiratory failure)
* Hemodynamic instability requiring vasopressor support
* Life support measures, including continuous renal replacement therapy (CRRT) or ECMO
* Altered mental status impairing participation (delirium requiring restraints)
* Glasgow Coma Scale (GCS) \< 13 or inability to follow commands
Source: ClinicalTrials.gov (NCT07618559). StuddyBuddy aggregates publicly available trial information.