Health Education for Improved Quality of Life and Reduced Anxiety and Depression in Ostomy Patients
This study aims to provide health education to improve the quality of life and reduce anxiety and depression in individuals living with an ostomy.
Health Education
Treatment Adherence and Compliance+24
+ Adherence Interventions
+ Anxiety Disorders
Supportive Care Study
Summary
Study start date: March 4, 2026
Actual date on which the first participant was enrolled.This study focuses on understanding the benefits of health education provided by nurses to adults who have undergone an ostomy, a type of digestive surgery. The main goal is to see if this education can help reduce feelings of anxiety and depression and improve the overall quality of life for these patients. The study is being conducted at the Ostomy Clinic of the University Hospital Complex of Santiago de Compostela and is designed for adults who have had an elimination ostomy, excluding terminal patients and those with cognitive impairments. The study aims to address the challenges faced by ostomy patients, potentially leading to improved care and quality of life for them. During the study, patients will receive health education workshops and continuous support from specialized nursing staff from the time they are admitted to the hospital until several months after the health education program is completed. The effectiveness of this education will be measured using validated scales for quality of life, anxiety, and depression. These measurements will help determine if the health education intervention is successful in achieving its goals.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.70 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 18 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Adults * Patients with digestive ostomies, either permanent or temporary ostomies lasting more than 6 months, attending ostomy consultations. * Volunteers with permanent digestive ostomies from the Santiago and Barbanza healthcare area. * Patients who agree to participate in the study. Exclusion Criteria: * Terminal patients * Patients with cognitive impairments
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Complejo Hospitalario Universitario de Santiago de Compostela
Santiago de Compostela, SpainOpen Complejo Hospitalario Universitario de Santiago de Compostela in Google Maps