GUSS-ICU Safe Nutrition Program After Extubation in ICU Patients
- Sponsor
- Istanbul University - Cerrahpasa
- Study ID
- NCT07195383
- Status
- Recruiting
Conditions
- Dysphagia
- Dysphagia, Swallowing Function, Diet Modification, Dysphagia Diet, Diet Standardization
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nutrion plan based on GUSS-ICU scale — OTHERTo ensure a rapid and accurate transition to post-extubation nutrition, patients will be assessed using the GUSS-ICU scale at 4 hours after extubation. A nutrition plan will be created based on the patient's GUSS-ICU score and will be maintained for 4 days.
Study Details
The aim of this study is to evaluate the effects of using the GUSS-ICU Safe Nutrition Program after extubation in Intensive Care Unit patients. This randomized controlled trial will be conducted in the Anesthesia Intensive Care Unit of Bakırköy Dr. Sadi Konuk Training and Research Hospital. Eligible participants will be randomly assigned to either the control group (usual care/routine follow-up group) or the intervention group (GUSS-ICU patients). Patients undergoing GUSS-ICU assessment will continue the nutritional program, as directed by the scale, for four days. Data are recorded on the first and last day. The data will then be evaluated in conjunction with the control group data.
Key Dates
- First listed
- Sep 26, 2025
- Start date
- Mar 5, 2025
- Status verified
- Sep 2025
- Primary completion
- Mar 5, 2026
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 82 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- SUPPORTIVE_CARE
Arms
- Experimental: GUSS-ICU Applied GroupThe GUSS-ICU Scale, which is used for the transition to feeding of extubated patients, will be applied to the randomly selected intervention group included in the study, and feeding will be planned and continued for 4 days according to the score achieved.
- No Intervention: Routine Follow-up GroupRoutine care and follow-up will be applied to the randomly selected control group for 4 days after extubation.
Primary Outcome Measure
Changes in malnutrition risk scores and findings in intensive care patients who received a GUSS-ICU Safe Nutrition Program after extubation [ Time Frame: On the 1st and 4th days after extubation ]
Central Contacts
- Merve TURKAY+905313793706
- Zeliha TÜLEK+905327762993
Related Studies
- Non-invasive Markers of Esophageal Function in AdultsEnrolling By Invitation · Vanderbilt University Medical Center · Nashville, Tennessee
- Effect of Thickened Feeds on Swallow Physiology in Children With DysphagiaRecruiting · Boston Children's Hospital · Boston, Massachusetts
- A Digital Therapeutic Platform for Swallowing and Drooling Problems in Parkinson'sPHASE3 · Recruiting · Northwestern University · Evanston, Illinois
- Aspiration in Acute Respiratory Failure Survivors 2Recruiting · University of Colorado, Denver · Stanford, California