Skip to main content
Clinical Trials/NCT06320002
NCT06320002
Completed
N/A

Improving Biopsychosocial Outcomes With a Communication Intervention for Patients Undergoing Fecal Ostomy Surgery

Massachusetts General Hospital1 site in 1 country25 target enrollmentJune 13, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Surgery
Sponsor
Massachusetts General Hospital
Enrollment
25
Locations
1
Primary Endpoint
Intervention Acceptability
Status
Completed
Last Updated
5 months ago

Overview

Brief Summary

In this study the investigators will evaluate the acceptability of a communication intervention for fecal ostomy surgery (CI-oSurg) to address the needs of adults who are undergoing fecal ostomy surgery. The investigators will recruit 24 patients and 4 clinicians (surgical nurses, wound ostomy nurses). At least half of patients are 65 years or older to understand the unique needs of older adults recovering from fecal ostomy surgery that might impact intervention acceptability. Questionnaires will be administered at two time-points for patient participants: upon study start and 4 weeks after exposure to the intervention.

Detailed Description

In this study the investigators are trying to understand the feasibility and acceptability of a psychologically informed communication guide for fecal ostomy Surgery with the overall goal of improving biopsychosocial outcomes of patients undergoing fecal ostomy surgery. An estimated 100,000 people in the US undergo fecal ostomy surgery (colostomy or ileostomy) each year, frequently to address severe symptoms (i.e., obstruction, perforation, and incontinence) due to colorectal cancer, diverticulitis, and pelvic floor dysfunction. Complication rates after fecal ostomy surgery are high (up to 37%) with negative effects on patient and family quality of life. Surgeons do not traditionally identify and address health outcomes patients with serious illness prioritize when making treatment decisions, such as caregiver burden, loss of independence and psychosocial function. Communicating this information is key to address patient anxiety when facing major surgery and ensure caregiver preparedness among patients and families considering fecal ostomy surgery. Current surgical guidelines support the use of preoperative communication and education interventions to improve psychosocial adjustment after fecal ostomy surgery based on expert opinion. However, little evidence exists evaluating the impact of communication interventions or content needs of patients undergoing fecal ostomy surgery or their family. Despite these guidelines, a recent study notes that inadequate ostomy education remains a frequent concern among patients undergoing fecal ostomy surgery. Furthermore, patients' perception of inadequate education is associated with poor emotional, social, and marital outcomes after surgery. There is a critical need to address this deficit in communication quality between patients undergoing fecal ostomy surgery, their family, and surgical care providers. Our guiding hypothesis is that development of a Communication Intervention for fecal ostomy Surgery (CI-oSurg) is acceptable to patients and clinicians, and will ultimately reduce patient distress and improve quality of life.

Registry
clinicaltrials.gov
Start Date
June 13, 2024
End Date
November 1, 2025
Last Updated
5 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Christy E. Cauley, MD, MPH

Assistant Professor

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18 or older
  • English fluency and literacy
  • Patient planned to undergo elective fecal ostomy surgery

Exclusion Criteria

  • Deemed inappropriate by the surgery team
  • Unable to provide consent due to severe cognitive impairment or physiologic status (septic shock/intubated)

Outcomes

Primary Outcomes

Intervention Acceptability

Time Frame: 4 weeks after the intervention

The intervention acceptability will be assessed by cognitive interviews with participants

Secondary Outcomes

  • Intervention Usability(4 weeks after intervention use)

Study Sites (1)

Loading locations...

Similar Trials