RecruitingNot ApplicableNCT02526264

Evaluation of Quality of Life and Period of Hospitalization by Education

Clinical Trial to Evaluate Quality of Life, Period of Hospitalization and Complication Rates in Patients With Stoma Receiving Specific Preoperative Education vs. Standard Preoperative Education


Sponsor

Krankenhaus Nordwest

Enrollment

138 participants

Start Date

Nov 24, 2015

Study Type

INTERVENTIONAL

Conditions

Summary

Patients with colorectal cancer prior to stoma surgery are randomized to different preoperative education programs: (a) specific preoperative education, (b) standard preoperative education. Outcome measures are quality of life, period of hospitalization and complication rates.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is looking at whether a structured patient education program before surgery can improve quality of life and reduce the length of hospital stay for patients with colorectal cancer who will need a stoma (a surgically created opening in the abdomen for waste removal). **You may be eligible if...** - You have colorectal cancer requiring surgery that will include placement of a stoma - The surgery involves the left side of the colon - You speak German and live in Germany - Your general health status is good enough for the study (ECOG score of 3 or lower) - You have given your informed consent - You will be participating in the standard education program **You may NOT be eligible if...** - Your stoma surgery is being done as an emergency procedure - You have dementia - You have already had a stoma in the past - You are already working with a stoma therapist - Your colorectal cancer has come back (recurrence) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHEREducation program

Verbal education prior tu surgery administered to all patients in order to inform about the surgery and outcomes


Locations(2)

Sana Klinikum

Offenbach, Germany

Krankenhaus Nordwest

Frankfurt, Germany

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NCT02526264


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