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NCT07588321Completed

E-Health-Supported Preoperative Education

EVALUATION OF THE EFFECTIVENESS OF PRE-OPERATIVE EDUCATION PROVIDED TO PATIENTS UNDERGOING CHEST SURGERY VIA AN E-HEALTH APPLICATION: A RANDOMIZED CONTROLLED STUDY

Source: ClinicalTrials.gov · Last updated 14 May 2026

Brief summary (registry, in English)

In the context of patient education, the integration of mobile applications-an e-health modality-among healthcare professionals and patients has garnered significant attention alongside technological advancements. Mobile applications offer distinct advantages, notably the vast global population capable of accessing and utilizing these digital tools. A study evaluating the impact of mobile applications on the recovery of patients undergoing ambulatory surgery demonstrated that the quality of recovery was superior in the intervention group. In research investigating mobile application-based education following breast cancer surgery, significant improvements were observed in pain levels, affected shoulder functions, and anxiety levels within the intervention group . Among patients undergoing cardiac surgery, 98% of those who received education via a mobile application reported that the application was beneficial to their recovery process . Furthermore, in a study involving a mobile application for patients undergoing heart valve surgery, the intervention group exhibited significantly lower probabilities of hospitalization, emergency department visits, and complications . An integrative review of mobile applications in the health education of surgical patients noted that while research has involved bariatric, orthopedic, colorectal, mastectomy, urological, and neurological surgical patients, there is an emphasized need for further nursing research utilizing emerging communication technologies. To date, no studies evaluating the effectiveness of preoperative education delivered via mobile application for patients undergoing thoracic surgery have been identified. Initiating preoperative preparation for patients scheduled for thoracic surgery is anticipated to positively influence postoperative recovery and quality of life, highlighting the necessity for research in this domain.

Status (registry)
Completed
Study type
Interventional
Enrollment
128 (actual)
First submitted
22 Apr 2026
Start date
18 Oct 2024
Primary completion date
22 Sept 2025
Lead sponsor
Dokuz Eylul University
Diseases
Lung cancer
NCT number
NCT07588321

What you commit to

  • Study type: Interventional
  • Participants enrolled: 128
  • From 18 Oct 2024 to the primary completion date, 22 Sept 2025
  • 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.

Prior treatment

  • Patients scheduled for emergency thoracic surgery

Other

  • Patients with physical limitations that prevent mobilization or participation in study tests
  • Patients with cognitive impairments (as they may fail to provide accurate data via the app)

Who the study is looking for

  • Patients aged 18 years and older
  • Patients with full spatial and temporal orientation
  • Patients without significant hearing or vision impairments
  • Patients with the ability to read and write
  • Patients scheduled for elective thoracic surgery due to a lung mass
  • Patients who voluntarily agree to participate and provide written informed consent
  • Patients who own and can operate a smartphone

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
Home
Coordinator of this site? Confirm its status
IzmirTurkey (Türkiye)Unknown status

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