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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.
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.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| intervention group | Experimental | The group mobilized for at least 20 minutes 6 times a day with a modular medical equipment carrying vehicle |
|
| control group | No Intervention | The group mobilized for at least 20 minutes 6 times a day with a routin practice |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| mobilization with moduler medical equipment carring vehicle | Other | Mobilization of the patients was carried out with the vehicle in their modular vehicle. |
|
| Measure | Description | Time Frame |
|---|---|---|
| general comfort scale score | monitoring of changes in the general comfort levels of the patients during the intervention | first day and fifth day |
| Richard Campell sleep quality scale score | monitoring of changes in the sleep quality of the patients during the intervention | every day for five days |
| pain scale score | monitoring of changes in the pain levels of the patients during the intervention | every day for five days |
| patient mobility scale score | monitoring of changes in the mobility of the patients during the intervention | every day for five days |
| 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 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Pınar Dogan, Asst.Prof. | Medipol University | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Istanbul Medipol University | Istanbul | Turkey (Türkiye) |
Data from the study will be reported over the levels of change in maintenance results. The study report is aimed to be published as a clinical research report.
Data will be used for 2 years
increase in sleep, comfort and mobility level of patients mobilized with this tool, decrease in pain and drain removal time
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| ID | Term |
|---|---|
| D051346 | Mobility Limitation |
| D007319 | Sleep Initiation and Maintenance Disorders |
| D010146 | Pain |
| ID | Term |
|---|---|
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D020919 | Sleep Disorders, Intrinsic |
| D020920 | Dyssomnias |
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Interventional study with posttest control group
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| D012893 | Sleep Wake Disorders |
| D009422 | Nervous System Diseases |
| D001523 | Mental Disorders |
| D009461 | Neurologic Manifestations |