Enrolling by invitation

Health Education for Improved Quality of Life and Reduced Anxiety and Depression in Ostomy Patients

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Study Aim

This study aims to provide health education to improve the quality of life and reduce anxiety and depression in individuals living with an ostomy.

What is being tested

Health Education

Other
Who is being recruted

Treatment Adherence and Compliance+24

+ Adherence Interventions

+ Anxiety Disorders

Over 18 Years
See all eligibility criteria
How is the trial designed

Supportive Care Study

Interventional
Study Start: March 2026
See protocol details

Summary

Principal SponsorHospital Clinico Universitario de Santiago
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleEffectiveness of Health Education as a Nursing Intervention in Improving Quality of Life and Reducing Symptoms of Anxiety and Depression in Ostomy Patients Following Digestive Surgery: A Quasi-Experimental Study.
Principal SponsorHospital Clinico Universitario de Santiago
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

70 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Supportive Care Study

These studies explore ways to improve comfort and daily life for people living with a condition. They may focus on easing symptoms, reducing treatment side effects, or supporting overall well-being.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Treatment Adherence and ComplianceAdherence InterventionsAnxiety DisordersBehaviorMental DisordersBehavioral SymptomsColitisColitis, UlcerativeColonic DiseasesColonic NeoplasmsDepressionDigestive System DiseasesDigestive System NeoplasmsGastroenteritisGastrointestinal DiseasesGastrointestinal NeoplasmsHealth EducationIntestinal DiseasesIntestinal NeoplasmsNeoplasmsNeoplasms by SitePatient Acceptance of Health CarePatient ComplianceColorectal NeoplasmsInflammatory Bowel DiseasesHealth BehaviorMedication Adherence

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.
Treatment Groups

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Health education (emotional care, mindfulness, jacobson, quality of life, social, sexual, ...). Method: psicosocial/holistic

Study 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

Suspended

Complejo Hospitalario Universitario de Santiago de Compostela

Santiago de Compostela, SpainOpen Complejo Hospitalario Universitario de Santiago de Compostela in Google Maps
Enrolling by invitationOne Study Center