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NCT Number: NCT06053957

The Effect of Early Mobilization on Postoperative Recovery in Abdominal Surgery

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kubra Erturhan Turk

Sivas, 58140, Turkey (Türkiye)

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who are conscious,
  • Without cognitive or mental problems,
  • Undergoing elective abdominal surgery,
  • Aged 18 and above,
  • Without physical limitations preventing early mobilization,
  • Without active bleeding,
  • 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

Treatment and study plan

Early mobilization

Procedure

early mobilization program

Primary outcomes

  1. The time to start the first mobilization

    Time frame: The time of the first mobilization within the first 24 hours after the surgery will be recorded.

  2. Postoperative recovery index results

    Time frame: The postoperative recovery index will be applied at the 24th hour.

  3. Total mobilization time in the first 24 hours

    Time frame: Total mobilization time will be applied at the 24th hour.

Sponsors and collaborators

Lead sponsor

Cumhuriyet University

Other

Registry information

Official study title

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

Important dates

Study start
2023
Primary completion
2024
Study completion
2024
First posted
Sep 26, 2023
Registry last updated
Jun 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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