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Clinical Trials in Turkey / NCT07374380
Starting soon Not applicable

Nurse-Led Early Mobilization After Colorectal Surgery

NCT07374380 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-05
Last updated
2026-01-28

Condition(s) studied

Colorectal SurgeryEarly MobilizationPostoperative CarePostoperative Recovery

Investigational drug(s) / intervention(s)

Nurse-Led Early MobilizationStandard Mobilization Care

Nurse-Led Early Mobilization: 1. Preoperative Period Patients will receive verbal education regarding the purpose, benefits, and process of early mobilization. To support this education, a Postoperative Mobilization Information Brochure prepared by the researchers will be provided to the patient and their caregiver. 2. Postoperative Day 0 Within the first 6-8 hours after surgery, vital signs will be monitored, and mobilization will be initiated in clinically stable patients under nurse supervision. 2.1. In-Bed Activities (Postoperative Hour 5) The following lower-extremity exercises will be performed: Ankle dorsiflexion and plantar flexion Toe movements Leg extension without knee flexion Circular foot movements Each exercise will be performed 5-10 repetitions. The patient will then be positioned in an upright sitting position in bed. 2.2. First Standing and Ambulation (Postoperative Hours 6-8) Vital signs will be assessed. The patient will be assisted to sit at the bedside for 1-2 minutes under nurse

Standard Mobilization Care: Participants in the control group will receive standard postoperative mobilization care routinely provided in the institution. Mobilization activities will be performed according to existing clinical practices, and no structured or protocol-based nurse-led early mobilization program will be implemented. Participants in the control group will continue to receive usual nursing care without any disadvantage or additional risk in terms of patient care.

Study summary

This study was designed to evaluate the effectiveness of a nurse-led early mobilization protocol on postoperative recovery outcomes in patients undergoing elective colorectal surgery. The outcomes assessed include walking distance, mobility levels, gastrointestinal function (time to first flatus and first defecation), nausea, vomiting, comfort, fatigue, time to initiation of oral intake, patient satisfaction, incidence of postoperative complications, and length of hospital stay.

Research Question:

In patients undergoing colorectal surgery (P), does a nurse-led early mobilization protocol (I), compared with standard mobilization practices (C), improve postoperative recovery outcomes (O), including walking distance, mobility levels, gastrointestinal function (time to first flatus and first defecation), nausea, vomiting, comfort, fatigue, time to initiation of oral intake, patient satisfaction, postoperative complication rates, and length of hospital stay?

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults aged 18 years and older * Scheduled for elective colorectal surgery (e.g., procedures related to * colorectal cancer, diverticulitis, or inflammatory bowel disease \[IBD\]) * Able to ambulate independently preoperatively * Medically and cognitively able to participate in a mobilization protocol * Able to provide written informed consent Exclusion Criteria: * Undergoing emergency colorectal surgery * Patients requiring postoperative intensive care unit (ICU) admission * Severe cognitive impairment or psychiatric disorders that may affect participation * Musculoskeletal or neurological conditions that impair mobility * Inability to understand study instructions due to language or communication barriers

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Ege University Izmir Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07374380 on ClinicalTrials.gov ↗ ← All trials in Turkey