- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06901050
Effect of FAST HUGS WITH ICU Approach on Length of Intensive Care Unit Stay in Patients With Hypoxic Respiratory Failure
March 23, 2025 updated by: Muş Alparslan University
Effect of FAST HUGS WITH ICU Approach on Length of Intensive Care Unit Stay in Patients With Hypoxic Respiratory Failure: A Randomized Controlled Trial
This study will investigate the effect of the FAST HUGS WITH ICU approach on the length of stay in the intensive care unit in patients with hypoxic respiratory failure.
Patients will be randomly assigned to the experimental and control groups.
The standard procedure will be applied to the control group.
The FAST HUGS WITH ICU approach will be applied to the experimental group.
We plan to follow up patients with Hypoxic Respiratory Failure using the abbreviation FAST HUGS WITH ICU (Feeding, Analgesia, Sedation, Thromboembolic prophylaxis, Head of bed elevation, Stress Ulcer prophylaxis and Glucose control Spontaneous breathing trial, Water Balance and constipation, Investigation and results, Therapy, Hypo-hyper delirium, Invasive devices, Check the daily infection parameters, Use a checlist).
The two groups will be examined in terms of hospital stay and some blood gas parameters.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Detailed Description
Hypoxic respiratory failure is responsible for 1.9 million patient admissions per year in the United States alone, and the hospital mortality rate is as high as 20%.
This rate is also increasing in Turkey.
The most common causes include pneumonia, cardiogenic pulmonary edema, ARDS, and chronic obstructive pulmonary disease (COPD).
Fast hugs is important in affecting the prognosis of patients with hypoxic respiratory failure in special clinics such as the Chest Diseases Intensive Care Unit.
Therefore, new studies are needed.
This study will investigate the effect of the FAST HUGS WITH ICU approach on the length of stay in the intensive care unit in patients with hypoxic respiratory failure.
Patients will be randomly assigned to the experimental and control groups.
The standard procedure will be applied to the control group.
The FAST HUGS WITH ICU approach will be applied to the experimental group.
We plan to follow up patients with Hypoxic Respiratory Failure using the abbreviation FAST HUGS WITH ICU (Feeding, Analgesia, Sedation, Thromboembolic prophylaxis, Head of bed elevation, Stress Ulcer prophylaxis and Glucose control Spontaneous breathing trial, Water Balance and constipation, Investigation and results, Therapy, Hypo-hyper delirium, Invasive devices, Check the daily infection parameters, Use a checlist).
The two groups will be examined in terms of hospital stay and some blood gas parameters.
Study Type
Interventional
Enrollment (Estimated)
34
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Eda Ay, Dr.
- Phone Number: (0442) 344 66 66
- Email: memnuniyet@atauni.edu.tr
Study Locations
-
-
-
Erzurum, Turkey, 25040
- Recruiting
- Atatürk University Research Hospital
-
Contact:
- Eda Ay, Dr
- Phone Number: 0442 344 6666
- Email: memnuniyet@atauni.edu.tr
-
Principal Investigator:
- Gamze KOÇ, Specialist
-
Sub-Investigator:
- Burak YAVUZ, Specialist
-
Sub-Investigator:
- Bahar ÇİFTÇİ, Associate Professor
-
Sub-Investigator:
- Hanım Duru YÜCE BAŞARAN, Specialist
-
Sub-Investigator:
- Dilara KOÇYİĞİT, Specialist
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being over 18 years old
- Being in the Chest Intensive Care Unit
- Having Hypoxic Respiratory Failure
Exclusion Criteria:
- Death during hospitalization
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Single Group Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Experimental Group
The FAST HUGS WITH ICU approach will be applied to the experimental group.
We plan to follow up patients with Hypoxic Respiratory Failure using the abbreviation FAST HUGS WITH ICU (Feeding, Analgesia, Sedation, Thromboembolic prophylaxis, Head of bed elevation, Stress Ulcer prophylaxis and Glucose control Spontaneous breathing trial, Water Balance and constipation, Investigation and results, Therapy, Hypo-hyper delirium, Invasive devices, Check the daily infection parameters, Use a checlist).
|
FAST HUGS WITH ICU; It is an abbreviation of "Feeding, Analgesia, Sedation, Thromboembolic prophylaxis, Head of bed elevation, Stress Ulcer prophylaxis and Glucose control Spontaneous breathing trial, Water Balance and constipation, Investigation and results, Therapy, Hypo-hyper delirium, Invasive devices, Check the daily infection parameters, Use a checlist".
With this approach, patients will be followed up.
|
|
No Intervention: Control Group
The standard procedure will be applied to the control group.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
length of hospital stay
Time Frame: 1 month
|
The difference between the duration of participants' admission to the intensive care unit and the time they are discharged from the intensive care unit will be examined.
|
1 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Güzel Nur YILDIZ, Dr, Muş Alparslan University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2024
Primary Completion (Estimated)
March 30, 2025
Study Completion (Estimated)
April 30, 2025
Study Registration Dates
First Submitted
March 23, 2025
First Submitted That Met QC Criteria
March 23, 2025
First Posted (Actual)
March 28, 2025
Study Record Updates
Last Update Posted (Actual)
March 28, 2025
Last Update Submitted That Met QC Criteria
March 23, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- MuşAlparslan
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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