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Clinical Trials in Turkey / NCT06679478
Enrolling by invitation Not applicable

Evaluation of Early Mobilization Protocol in Patients Undergoing Gastrointestinal Surgery

NCT06679478 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-11-11
Last updated
2024-11-13

Condition(s) studied

Gastrointestinal Diseases

Investigational drug(s) / intervention(s)

Enhanced Recovery After Surgery (ERAS) Early Mobilization Protocol

Enhanced Recovery After Surgery (ERAS) Early Mobilization Protocol: The intervention is applied from the first day after surgery until discharge. (including the day of discharge).

Study summary

In this study, the investigators aimed to evaluate the early mobilization protocol created in accordance with the accelerated recovery guide after surgery in patients undergoing gastrointestinal surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Being 18 years of age or older * Agreeing to participate in the study * Being able to understand, speak Turkish or have no obstacle to communication * Having undergone open gastrointestinal surgery * Having an American Society of Anesthesiologists (ASA) score \<IV * Being fully independent according to the Modified Barthel Index during the pre-operative period * Staying in the hospital for at least 48 hours after the surgery * Having a phone * Agreeing to download the 'StepsApp Pedometer' application to their phone * Agreeing to carry the phone with them during the post-operative mobilization processes Exclusion Criteria: * Being taken into emergency surgery * Having had major gastrointestinal surgery before * Having a diagnosis that may restrict mobilization (neurological, cardiovascular, respiratory and musculoskeletal comorbidities) * High risk of falling in the preoperative period * Using medication that may affect mobilization * Having a diagnosis of any psychiatric disease * Having a Nutritional Risk Score score of ≥3 * Being in contact isolation * Being morbidly obese * Being in intensive care for more than 24 hours during the postoperative period * Having an intubation period of more than 24 hours during the postoperative period * Developing a complication that may prevent mobilization after surgery * Withdrawing from participating in the study,

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Derya Şayır Köksal Kütahya 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 NCT06679478 on ClinicalTrials.gov ↗ ← All trials in Turkey