Air Suspension Biodegradable Patient Transport Pad
The Design and Application of Air Suspension Biodegradable Patient Transport Pad
On the one hand, transferring patient from bed to bed is usually handling by the manual lifting of several staffs or utilizing bedsheet, slide sheet , shovel-style stretcher or other devices to move and lift patients. Whatever, there are some advantages using these devices.
On the other hand, nurses are among the professionals at the highest risk for musculoskeletal disorders. The Bureau of Labor Statistics has shown that overexertion in manual lifting was the main event or exposure leading to injury or illness involving time away from work. Excessive weights, awkward postures, and repetitive motions are some of the known risk factors that contribute to sprains/strains and back injuries. During the process of patient transferring , it refers to the above risk factors for health-care workers. It recommended that using appropriate assistive equipment can reduce the injuries. If staff is safe, patients are safer.
The research team has designed and produced a new transport assistive devices-- biodegradable and air-suspending transfer mattress, which was precisely controlled by gas flow and based on ergonomics. And then apply it to the clinic in order to find whether it's benefit for patients and nursing staff.
It is a randomized controlled trial design.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
Research design：randomized controlled trials. Computer generated random numbers. The patients were randomly divided into three groups, ① transfer patients by air-suspending mattress, ② transfer patients by slide board, ③ transfer patients by bedsheets.
Participants: passive patient with transports needs, such as CT/ MRI examination etc. The sample size estimation was according to the formula of multiple parallel design. The main outcome measure was the perceived exertion.
Studientyp
Einschreibung (Voraussichtlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Zhejiang
-
Hangzhou, Zhejiang, China, 310009
- Second Affiliated Hospital, School of Medicine, Zhejiang University
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Passive patient with transfer requirements, such as CT/ MRI examination , transfer from one department to another etc；Patients or their family signed an informed consent.
Exclusion Criteria:
- The patients weighted over 150kg and have spine fracture ；age< 15 years old.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Experimental group
Patients in experimental group were transferred by air-suspending mattress.
|
Put mattress in advance on the bed.
When patients need to be transferred from bed to bed, fill the mattress with gas and keep it inflated, then pull the mattress .
|
|
Aktiver Komparator: control group 1
Patients in control group 1 were transferred by slide board.
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When patients need to be transferred from bed to bed, insert slide board under patient, then pull the slide board.
|
|
Aktiver Komparator: control group 2
Patients in control group 2 were transferred by bedsheet.
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When patients need to be transferred from bed to bed, just lift the bedsheet.
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Force value
Zeitfenster: Day 1
|
Spring balance was used to measured the pulling force while transferring patients.(Force
value in N)
|
Day 1
|
|
perceived exertion
Zeitfenster: Day 1
|
Perceived exertion was evaluated by using the Borg Scale of 6-20, which the values near 6 and 20 represent low and high physical exertion, respectively.（perceived
exertion in scores）
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Day 1
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
respiration rate
Zeitfenster: Day 1（before and after transferring）
|
Be recorded by ECG monitor the moment before and after transferring.（respiration
rate in bpm）
|
Day 1（before and after transferring）
|
|
blood pressure
Zeitfenster: Day 1（before and after transferring）
|
Be recorded by ECG monitor the moment before and after transferring.(blood
pressure in mmHg)
|
Day 1（before and after transferring）
|
|
heart rate
Zeitfenster: Day 1（before and after transferring）
|
Be recorded by ECG monitor the moment before and after transferring.（heart
rate in bpm）
|
Day 1（before and after transferring）
|
|
oxygen saturation
Zeitfenster: Day 1（before and after transferring）
|
Be recorded by ECG monitor the moment before and after transferring.
|
Day 1（before and after transferring）
|
|
Transfer time
Zeitfenster: Day 1
|
Stopwatch was used to record the time from using the assistive devices to moving the patients to another bed.（transfer
time in minutes）
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Day 1
|
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Satisfaction of patient
Zeitfenster: Day 1
|
Self-made satisfaction questionnaire was used to get the patients' satisfaction about the assistive devices after transferring patients.It includes five items about the feelings of assistive devices while moving--comfort, safety, pain, stability and sound.
All the answers take five levels, level five means very satisfied and level one represents very dissatisfied.(Satisfaction of patient in scores)
|
Day 1
|
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Satisfaction of nurse staff
Zeitfenster: Day 1
|
Self-made satisfaction questionnaire was used to get nurse staffs' satisfaction about the assistive devices after transferring patients.
It includes seven items about using the devices to move patients --no adverse events, saving energy, saving time, convenience, applicability, strong support and total satisfaction.
All the answers take five levels, level five means very satisfied and level one represents very dissatisfied.(Satisfaction of patient in scores)
|
Day 1
|
Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Jingfen Jin, Master, The Second Affiliated Hospital of Medical College of Zhejiang University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Voraussichtlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2018PY011
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
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