RecruitingNot ApplicableNCT07163247

Effectiveness of Pet-Robotic Intervention in Intensive Care Unit Patients

Effectiveness of Using Pet-Robotic Intervention to Enhance Spontaneous Breathing Trial Success in Intensive Care Unit Patients

Sponsor

National Taiwan University Hospital

Enrollment

24 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Spontaneous Breathing Trial in ICU Spontaneous Breathing Trial

Summary

This study aims to develop a novel nursing intervention involving robotic pet companionship to reduce anxiety in patients undergoing spontaneous breathing trials.

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether interactions with a robotic pet can reduce stress and anxiety in ICU patients who have been on a breathing machine (ventilator) for an extended time and are preparing to breathe on their own again. The goal is to ease psychological distress during a difficult recovery process. **You may be eligible if...** - You are 18 or older and awake and aware - You have been on a ventilator for more than 72 hours - You previously failed a breathing trial but are now ready to try again **You may NOT be eligible if...** - You have a drug-resistant infection - You need airborne isolation (e.g., active COVID-19) - You have a severely weakened immune system (very low white blood cell count) - You are heavily sedated - You have a tracheostomy (breathing tube in the neck) - You have an implanted heart device (pacemaker, defibrillator) - You are known to be allergic to robotic pet fur Talk to your doctor to see if this trial is right for you.

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Interventions

BEHAVIORALRobotic pet (PARO) companionship

The intervention is composed of the following components: Duration: Robotic pet companionship lasting 30-120 minutes, depending on clinical goals during each spontaneous breathing trial (SBT). Preparation and interaction: PARO is introduced 30 minutes before each SBT to establish emotional connection. Study staff will briefly introduce its interactive features, including responding to stroking, gentle tapping, head movements, and eye blinking. Participants may interact freely with PARO during the intervention. Assessment: Outcome measurements are conducted during the intervention. If extubated successfully, a semi-structured interview is conducted three days later. Early termination: The intervention is stopped if the participant becomes clinically unsuitable for further SBTs or experiences a serious adverse event (e.g., device dislodgement). Additional information: After each SBT, PARO is sterilized and stored in a sealed container in the patient's room.

Locations(1)

National Taiwan University Hospital

Taipei, Taiwan

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NCT07163247

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