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NCT07347158Enrolling by invitation

Effectiveness 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.

Source: ClinicalTrials.gov · Last updated 16 Jan 2026

Brief summary (registry, in English)

The proposed project is a prospective quasi-experimental study to be conducted at the Ostomy Clinic of the University Hospital Complex of Santiago de Compostela. The primary objective is to evaluate the effectiveness of health education as a nursing intervention in reducing anxiety and depression and improving the quality of life of ostomy patients following digestive surgery. The study will focus on adult patients who have undergone an elimination ostomy, excluding terminal patients and those with cognitive impairments. The study involves clinical follow-up of patients from hospital admission to several months after completing the health education program. Validated scales will be used to measure quality of life, anxiety, and depression. The intervention will consist of health education workshops and continuous follow-up by specialized nursing staff.

Status (registry)
Enrolling by invitation
Study type
Interventional
Enrollment
70 (estimated)
First submitted
4 Dec 2025
Start date
4 Mar 2026
Primary completion date
31 Oct 2026
Lead sponsor
Hospital Clinico Universitario de Santiago
NCT number
NCT07347158

What you commit to

  • Study type: Interventional
  • Planned participants: 70
  • From 4 Mar 2026 to the primary completion date, 31 Oct 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Terminal patients
  • Patients with cognitive impairments

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Complejo Hospitalario Universitario De Santiago De Compostela
Coordinator of this site? Confirm its status
Santiago de CompostelaSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.