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Effect of Mobilization Protocol on Mobilization

Effect of Mobilization Protocol on Mobilization Start Time and Patient Care Results in Patients Undergoing Abdominal Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04730141
Enrollment
42
Registered
2021-01-29
Start date
2019-05-29
Completion date
2020-03-27
Last updated
2021-01-29

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

Conditions

Abdominal Surgery, Nursing

Keywords

surgery and mobilization, early mobilization protocol

Brief summary

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

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.

Interventions

OTHERPatient mobilization with pre-operative mobilization training and mobilization protocol

Postoperative mobilization for the first 24 hours

Sponsors

Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE

Intervention model description

quasi-experimental study

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
The effect of mobilization protocol on mobilization start timefirst 24 hours postoperatifIn the postoperative period, the hour of mobilization of the patient was recorded.The group in which the mobilization protocol was applied and the group in which the mobilization protocol was not applied were compared
Postoperative sleep qualityPostoperative 24th hourVAS is considered a valid, reliable and usable measurement tool used to convert some values that cannot be measured numerically into numericals. Possible scores from 0 (worst case) to 10 (best case)
Postoperative patient satisfactionPostoperative 24th hourVAS is considered a valid, reliable and usable measurement tool used to convert some values that cannot be measured numerically into numericals. Possible scores from 0 (worst case) to 10 (best case)

Secondary

MeasureTime frameDescription
Postoperative number of stepsThe total number of steps taken during the first 24 hours postoperativelyPedometer programs are easy-to-use mobile applications where features such as the number of steps taken at a given time and walking distance can be recorded. Pedometer application is downloaded to the phone, the number of steps and walking distance are recorded by carrying it in a pocket or bag. In this study, Developer: ITO Technologies Inc, category: health and fitness, version 1.1.10 pedometer program was used.

Countries

Turkey (Türkiye)

Outcome results

None listed

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