This study is currently not recruiting participants.

A Prospective Single-Center Study to Assess the Impact of Pre- and Post-Surgical Ostomy Care Education on Patient Outcomes and Quality of Life

Study on the Effectiveness of Ostomy Education

Not Recruiting
18 years - 100 years
All
Phase N/A

Brief description of study.

The purpose of this study is to evaluate the effectiveness of pre-operative and post-operative ostomy education compared to standard of care ostomy education.

Detailed description of study

The purpose of this study is to evaluate the effectiveness of pre-operative and post-operative ostomy education compared to standard of care ostomy education.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Ostomy
  • Age: 18 years - 100 years
  • Gender: All

This study investigates the effectiveness of ostomy education given before and after surgery compared to the standard ostomy education usually provided. An ostomy is a surgical procedure where an opening is made in the body to discharge waste. The study aims to understand if timing and method of education can improve outcomes for patients undergoing this procedure.

Participants in the study will receive either pre-operative and post-operative education or the standard care education. The study will compare these groups to see which approach provides better support and understanding for patients.

  • Who can participate: Adults aged 18 and older who are scheduled to undergo ostomy surgery are eligible to participate. Key eligibility factors include being able to provide informed consent and not having prior ostomy surgery.
  • Study details: Participants will receive educational sessions either before and after their surgery or as per the standard care protocol. The study will evaluate the impact of these educational approaches on patient outcomes.
Updated on 19 Feb 2024. Study ID: 1202007926

Interested in the study?

Select a study center that’s convenient for you, and get in touch with the study team.

Connect with the study team