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The Effect of Early Mobilization on Postoperative Recovery in Abdominal Surgery

The Effect of Early Mobilization on Postoperative Recovery in Abdominal Surgery: A Randomized Controlled Study

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06053957
Enrollment
130
Registered
2023-09-26
Start date
2023-09-16
Completion date
2024-02-29
Last updated
2026-09-01

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

Conditions

Early Ambulation, Nursing Caries

Keywords

nursing, early mobilization, postoperative care, recovery

Brief summary

Objectives: This study will be conducted to determine the effect of early mobilization on postoperative recovery in abdominal surgery patients.. Methods: This research is a randomized controlled experimental study. In the Gastrointestinal Surgery Department, a total of 130 patients will be included, consisting of 65 experimental group and 65 control group, who are scheduled for abdominal surgery in the study. In the study, data will be collected using a survey form, Numerical Rating Scale, gradual mobilization chart in the first 24 hours after surgery, and Postoperative Recovery Index (PoRI-TR). On the day before the surgery, the experimental group will receive early mobilization training. On the day of the surgery, vital signs, oxygen saturation, and pain intensity will be assessed before the first mobilization. Pain control will be ensured before mobilization. Each mobilization will be carried out in accordance with the gradual mobilization schedule within the first 24 hours after surgery. Following the Enhanced Recovery After Surgery (ERAS) protocol recommendation, mobilization will be provided outside of bed for a total of 2 hours, with durations increasing by the hour on the day of surgery under the supervision of the researcher: 5, 15, 25, 35, and 40 minutes. Mobilizations for patients showing signs of orthostatic hypotension will be postponed by 30 minutes. On the days following the surgery, patients will be informed to spend 6 hours outside of bed. The control group will receive routine care procedures. The second part of the questionnaire will be administered on the day of the surgery for both the experimental and control groups, and the PoRI-TR will be applied at the 25th hour after surgery. Data will be collected through face-to-face interviews within 20-25 minutes. The data obtained from the research will be evaluated using the SPSS 22.00 program. The normality of the data will be determined by Skewness-Kurtosis tests. Based on this result, either parametric or non-parametric tests will be applied.

Interventions

PROCEDUREearly mobilization

early mobilization program

Sponsors

Cumhuriyet University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Patients who are conscious, * No physician-diagnosed psychiatric problems, * Undergoing elective abdominal surgery, * Aged 18 and above, * Without physical limitations preventing early mobilization, * Without cardiovascular or respiratory diseases, * Classified as American Society of Anesthesiologists (ASA) class I or II, * Literate patients * Volunteering

Exclusion criteria

* Patients undergoing oncologic surgery who spend the first 24 hours in the intensive care unit due to post-operative care, * Emergency surgery patients due to the absence of pre-operative preparation phase, * Patients who are healthcare workers due to their knowledge about early mobilization * those who required intensive care after surgery, * those who had active bleeding after surgery, * those who experienced nausea and vomiting after surgery, * those whose symptoms of orthostatic hypotension recurred during mobilization after early mobilization was delayed for 30 minutes because of symptoms of orthostatic hypotension, * those whose vital signs were not normal.

Design outcomes

Primary

MeasureTime frame
The time to start the first mobilizationThe time of the first mobilization within the first 24 hours after the surgery will be recorded.
Postoperative recovery index resultsThe postoperative recovery index will be applied at the 24th hour.
Total mobilization time in the first 24 hoursTotal mobilization time will be applied at the 24th hour.

Secondary

MeasureTime frame
Length of hospital stay after surgeryFrom the date of surgery until the date of hospital discharge (approximately 1-2 days after surgery).
Total length of hospital stayFrom the date of hospital admission until the date of hospital discharge (approximately 3-4 days).

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 2, 2026