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Clinical Trials/NCT05081856
NCT05081856CompletedNot Applicable

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

Istanbul Medipol University Hospital1 site in 1 country83 target enrollmentStarted: October 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
83
Locations
1
Primary Endpoint
Richard Campell sleep quality scale score

Study Overview

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.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts 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

Arms & Interventions

intervention group

Experimental

The group mobilized for at least 20 minutes 6 times a day with a modular medical equipment carrying vehicle

Intervention: mobilization with moduler medical equipment carring vehicle (Other)

control group

No Intervention

The group mobilized for at least 20 minutes 6 times a day with a routin practice

Outcomes

Primary Outcomes

Richard Campell sleep quality scale score

Time Frame: every day for five days

monitoring of changes in the sleep quality of the patients during the intervention

pain scale score

Time Frame: every day for five days

monitoring of changes in the pain levels of the patients during the intervention

general comfort scale score

Time Frame: first day and fifth day

monitoring of changes in the general comfort levels of the patients during the intervention

drain removal time (day (median))

Time Frame: the day the drain was removed

monitoring of changes in the drain removal time of the patients during the intervention

patient mobility scale score

Time Frame: every day for five days

monitoring of changes in the mobility of the patients during the intervention

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Istanbul Medipol University Hospital
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

pınar dogan

Asst.Prof.

Istanbul Medipol University Hospital

Study Sites (1)

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