Multisensory and Cognitive Interventions in the ICU: Effects on Health and Recovery

Recruiting now · Not applicable

Conditions studied: Coronary Artery Bypass Graft (CABG), Cardiac Surgery Subjects, Postoperative Care

In brief

The goal of this clinical trial is to examine the effects of sensory and cognitive stimulation on physiological, psychological, and functional recovery in adult patients after cardiac surgery who are treated in the intensive care unit (ICU). The main questions it aims to answer are: * Does sensory and/or cognitive stimulation reduce anxiety and improve hemodynamic stability in ICU patients? * Does it enhance physical function and independence during early rehabilitation in the ICU? Researchers will compare four groups: 1. Standard care (control), 2. Cognitive stimulation, 3. Auditory stimulation (music), 4. Multisensory stimulation (touch + smell) to assess which intervention is most effective in improving recovery parameters. Participants will: * Be randomly assigned to one of four groups during early mobilization in the ICU * Receive a 30-minute intervention session depending on group assignment * Be evaluated for heart rate, blood pressure, oxygen saturation, anxiety (VAS), physical function (PFIT, FIM), and satisfaction before and after the session

Key facts

Study ID

NCT07116941

Run by

Abant Izzet Baysal University

People needed

125

Starts

2025-08-01

Expected to finish

2026-06-30

Last updated by the study team

2026-02-12

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age between 18 and 80 years
• Underwent coronary artery bypass grafting (CABG) or other open-heart surgery
• Admitted to the ICU postoperatively and eligible for early mobilization
• Hemodynamically stable (within normal blood pressure and heart rate ranges, without inotropic support)
• Alert and able to communicate

You may not qualify if…

• Diagnosis of ICU delirium or altered mental status
• Severe hemodynamic instability
• Presence of neurological disease or significant cognitive impairment
• Significant sensory deficits (e.g., severe hearing or vision loss)
• Known allergy or psychological sensitivity to auditory or olfactory stimuli (e.g., aromatherapy or music)

Where it is running

• Bolu Abant Izzet Baysal University, Izzet Baysal Training and Research Hospital — Bolu, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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