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Use Modular Medical Equipment Vehicle in Mobilization of Patient With Chest Tube

The Effect of Modular Carrying System on Patient Outcomes in the Mobilization of Patients With a Chest Tube

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05081856
Enrollment
83
Registered
2021-10-18
Start date
2019-10-01
Completion date
2021-01-15
Last updated
2024-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comfort, Mobility Limitation, Pain, Sleep Quality, Time of the Removal Chest Tube

Keywords

care outcomes, mobilization, chest tube

Brief summary

in this study, it was aimed to examine the effect of the modular carrying system on the outcomes of care in the mobilization of patients with a chest tube. The population of the study consisted of patients followed in Yedikule Chest Diseases, and Thoracic Surgery Training and Research Hospital between October 2019 and January 2021, and the sample consisted of 83 patients who met the inclusion criteria. The study was performed with the intervention group (n=37) mobilized with the Modular medical equipment carrying vehicle and the control group (n=46) mobilized with the routine application.

Detailed description

Within the scope of the study, a Modular medical equipment carrying vehicle was developed by the researchers to ensure the safe and comfortable mobilization of patients with chest tube and additional medical equipment. This vehicle has been designed to maintain the level of the chest tube during mobilization and to prevent it from tipping over.Patients in the intervention group were mobilized with the help of this Modular medical equipment carrying vehicle for 20 minutes at least 6 times a day. Patients in the control group were mobilized at least 6 times a day for 20 minutes with clinical routine practice.

Interventions

OTHERmobilization with moduler medical equipment carring vehicle

Mobilization of the patients was carried out with the vehicle in their modular vehicle.

Sponsors

Istanbul Medipol University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

Interventional study with posttest control group

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* chest tube inserted due to open surgery, hemodynamically stable, followed up in the clinic for at least 5 days, first mobilized after chest tube inserted

Exclusion criteria

* have a mental or psychological illness, hemodynamically unstable

Design outcomes

Primary

MeasureTime frameDescription
general comfort scale scorefirst day and fifth daymonitoring of changes in the general comfort levels of the patients during the intervention
Richard Campell sleep quality scale scoreevery day for five daysmonitoring of changes in the sleep quality of the patients during the intervention
pain scale scoreevery day for five daysmonitoring of changes in the pain levels of the patients during the intervention
patient mobility scale scoreevery day for five daysmonitoring of changes in the mobility of the patients during the intervention
drain removal time (day (median))the day the drain was removedmonitoring of changes in the drain removal time of the patients during the intervention

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026