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

Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05081856
• Other study ID #: 12093487
• Status: Completed
• Phase: N/A
• Start date: October 1, 2019
• Est. completion date: January 15, 2021

Study information

• Verified date: August 2021
• Source: Istanbul Medipol University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 83
• Est. completion date: January 15, 2021
• Est. primary completion date: May 15, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

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

Related Conditions & MeSH terms

• Comfort
• Mobility Limitation
• Pain
• Sleep Quality

Intervention

Other:
• mobilization with moduler medical equipment carring vehicle
Mobilization of the patients was carried out with the vehicle in their modular vehicle.

Locations

Country	Name	City	State
Turkey	Istanbul Medipol University	Istanbul

Sponsors (1)

Lead Sponsor	Collaborator
Istanbul Medipol University Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	general comfort scale score	monitoring of changes in the general comfort levels of the patients during the intervention	first day and fifth day
Primary	Richard Campell sleep quality scale score	monitoring of changes in the sleep quality of the patients during the intervention	every day for five days
Primary	pain scale score	monitoring of changes in the pain levels of the patients during the intervention	every day for five days
Primary	patient mobility scale score	monitoring of changes in the mobility of the patients during the intervention	every day for five days
Primary	drain removal time (day (median))	monitoring of changes in the drain removal time of the patients during the intervention	the day the drain was removed