Study Results
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Basic Information
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NOT_YET_RECRUITING
NA
80 participants
INTERVENTIONAL
2024-11-01
2025-09-01
Brief Summary
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Detailed Description
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This study will be conducted to evaluate the effect of back support on patients undergoing transfemoral angiography on the patients' vital signs, which are defined as pulse, blood pressure, respiratory rate and blood oxygen saturation (SPO2), as well as comfort levels indicating satisfaction levels.
The study is planned to be completed between September 1, 2024 and April 1, 2025. The universe of the study, which was conducted as a randomized controlled trial model, consisted of patients who underwent angiography in the cardiovascular surgery intensive care units of Tunceli State Hospital. Randomization of the participants was planned to be assigned to the experimental and control groups via random.org (Back support group=40, Control group=40). "Patient Information Form", "Visual Analog Scale (VAS)" and "Immobilization Comfort Scale (IMC)" will be used in data collection. General linear model and mixed ANOVA analysis will be performed according to the characteristics of the data.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
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Back Gupport Group
After the transfemoral angiography procedure, the patient will be taken to bed and monitored. Approximately 2 hours after the procedure, under the control of the doctor and nurse, the sheath in the patient's groin area will be pulled and a 3 kg sandbag will be left. A 36x33x10 cm gel-containing visco pillow will be placed in the patient's lumbar cavity by the research nurse and primary nurse to fill the anatomical space. The patient will be monitored in a supine position with the head elevated (30 degrees) and blood pressure, pulse, respiratory rate, oxygen saturation and comfort and pain level will be recorded at 0, 3 and 6 hours.
Back Support
When the sandbag is to be left by the researcher together with the nurse caring for the patient, the patient will be placed in the left lateral position for a short time, a gel-filled orthopedic non-sweating viscose pillow will be placed in the patient's lumbar region and the patient will be placed in a supine position with the head supported.
Control Group
The patients in this group will be monitored in the supine position with the head elevated (30 degrees) without pillow support and blood pressure, pulse, respiratory rate, oxygen saturation and comfort and pain level will be recorded at 0, 3 and 6 hours.
No interventions assigned to this group
Interventions
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Back Support
When the sandbag is to be left by the researcher together with the nurse caring for the patient, the patient will be placed in the left lateral position for a short time, a gel-filled orthopedic non-sweating viscose pillow will be placed in the patient's lumbar region and the patient will be placed in a supine position with the head supported.
Eligibility Criteria
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Inclusion Criteria
* Patients who did not have verbal communication problems,
* Patients who consented to participate in the study were determined as patients.
Exclusion Criteria
* Have chronic low back pain,
* Have had previous back surgery/herniated disc,
* Have coagulation problems (PLT\<50000 mm3),
* Did not consent to participate in the study,
* Have communication problems.
18 Years
90 Years
ALL
No
Sponsors
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Inonu University
OTHER
Responsible Party
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Zeliha CENGİZ
associate proffesor
Locations
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Tunceli State Hospital
Tunceli, , Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Mehdi Onaç, specialist doctor
Role: primary
Other Identifiers
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2024/5744
Identifier Type: -
Identifier Source: org_study_id
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