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NCT06961539Completed

"The Effect of Virtual Visitation in the Intensive Care Unit on Pain, Anxiety, and Sleep Levels"

The Effect on Pain, Anxiety and Sleep Levels of Virtual Visiting in the Cardiovascular Surgery Intensive Care Unit: A Randomized Controlled Trial

Source: ClinicalTrials.gov · Last updated 8 May 2025

Brief summary (registry, in English)

Patients in the intensive care unit after cardiovascular surgery face not only complications related to the surgical procedure but also emotional distress due to separation from their loved ones. Because of infection control measures, visitor restrictions are enforced in intensive care units, which may further contribute to patient stress. This study aims to evaluate the effect of scheduled virtual visitation in the intensive care environment on patients' postoperative pain, anxiety, and sleep levels.

Status (registry)
Completed
Study type
Interventional
Enrollment
70 (actual)
First submitted
22 Apr 2025
Start date
1 Oct 2023
Primary completion date
31 Mar 2025
Lead sponsor
Saglik Bilimleri Universitesi
NCT number
NCT06961539

What you commit to

  • Study type: Interventional
  • Participants enrolled: 70
  • From 1 Oct 2023 to the primary completion date, 31 Mar 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.

Other illness

  • Patients with psychiatric disorders and using medication,

Other

  • Illiterate patients,
  • Patients without a relative who can conduct the virtual visit,
  • Patients with communication problems.

Who the study is looking for

  • Aged 40 and above,
  • Underwent elective coronary artery bypass graft surgery,
  • Conscious, extubated, and hemodynamically stable,
  • Glasgow Coma Scale score of 15,
  • Followed in the intensive care unit for at least 48 hours after surgery,
  • Patients who agreed to participate in the study.

Age in the registry: 40 years to - · Sex: All · Accepts 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
Hamidiye Institute of Health Sciences, University of Health Sciences
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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