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Effect of Mobilization Protocol on Mobilization

NCT ID: NCT04730141

Last Updated: 2021-01-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-05-29

Study Completion Date

2020-03-27

Brief Summary

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The aim of this study is to determine the effect of early mobilization protocol on patients' mobilization status and patient care outcomes in patients who undergo major abdominal surgery. This study is a prospective non-randomized controlled clinical trial.

Detailed Description

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The study sample consisted of 42 patients, 21 of whom were the control group and 21 were the intervention group, who had undergone major abdominal open surgery between May and September 2019. The routine mobilization follow-up approach of the intensive care unit was applied to the patients in the control group, and the early mobilization protocol developed by using up-to-date guidelines and expert opinions were applied to the patients in the intervention group. In the study, the data of the control group were firstly collected, then the early mobilization protocol was introduced to the patients through the training brochure prepared and then data of the intervention group were collected. In the study, the characteristics of the patients in both groups belonging to the preoperative period, the distance they walked in the 6-minute walking test and the results of the postoperative period were recorded.

Conditions

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Abdominal Surgery Nursing

Keywords

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surgery and mobilization early mobilization protocol

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SEQUENTIAL

quasi-experimental study
Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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mobilization protocol

The early mobilization protocol developed by using up-to-date guidelines and expert opinions were applied to the patients in the intervention group.

Group Type EXPERIMENTAL

Patient mobilization with pre-operative mobilization training and mobilization protocol

Intervention Type OTHER

Postoperative mobilization for the first 24 hours

routine care

The routine mobilization follow-up approach of the intensive care unit was applied to the patients in the control group .

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Patient mobilization with pre-operative mobilization training and mobilization protocol

Postoperative mobilization for the first 24 hours

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* To undergo major abdominal open surgery
* ASA \<IV
* Being over the age of 18
* Not having a barrier to communication
* Having agreed to participate in the study

Exclusion Criteria

* Being diagnosed that may limit mobilization
* Being diagnosed with chronic obstructive pulmonary disease
* ASA IV-V-VI
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

OTHER

Sponsor Role lead

Responsible Party

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Fadime Koyuncu

Research Assistant

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Emine Iyiun

Role: STUDY_DIRECTOR

Gulhane Hemsirelik Fakultesi

Locations

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Fadime

Ankara, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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19208

Identifier Type: -

Identifier Source: org_study_id