Can Wearable Technology Products Change Our Patient Management in Laparoscopic Colorectal Cancer Surgery

Ankara University

Status: Enrolling

Conditions: Ambulation Difficulty; Physical Examination

Treatments: Procedure: Mobilization recommendations

Study type: Interventional

Funder types: Other

Identifiers

NCT05598294

AnkaraUSurgOnc

Details and patient eligibility

About

The clinical progress of the patients whose mobilization the investigators follow up with wearable technology products will be observed in the early postoperative period until discharge. In this way, the investigators primarily aim to examine whether the bowel movements of our more mobilized patients return earlier.

Enrollment: 190 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients who underwent laparoscopic abdominal surgery
• Colorectal cancer patients
• Curative surgeries
• Stage 0,1,2,3 patients

Exclusion criteria

• Patients who cannot walk
• Patients converted to open procedure
• Patients with ostomy
• Patients for whom laparoscopy is contraindicated
• Palliative surgeries
• Patients with distant organ metastases

Trial design

Primary purpose: Screening

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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190 participants in 2 patient groups

Control Group

No Intervention group

Description:

Standard treatment and mobilization recommendations will be given to this group.

Mobilization Group

Experimental group

Description:

Mobilization of patients will be encouraged.

Treatment:

Procedure: Mobilization recommendations