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Trial Title: The Effect of Post-operative Exercise in Gastric Cancer Patients: A Randomized Controlled Trial (RCT) Study

NCT ID: NCT06260293

Condition: Gastric Cancer

Conditions: Official terms:
Stomach Neoplasms

Study type: Interventional

Study phase: N/A

Overall status: Active, not recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Supportive Care

Masking: None (Open Label)

Intervention:

Intervention type: Behavioral
Intervention name: exercise
Description: A total of 4 exercise interventions. Twice In-patient exercise interventions: exercises on the ward at POD1, and POD2, and Recommended walking and stretching. Twice home-based exercise interventions: post-discharge, Recommended 30 minutes of low to moderate-intensity walking and daily bodyweight exercises per day(150 minutes each week). and remote exercises 1 per week.
Arm group label: Exercise group

Summary: Medical advancements are enhancing the survival rates of individuals with gastric cancer. The growing population of gastric cancer survivors underscores the importance of managing treatment-related after-effects and side effects. Diminished physical function in cancer patients, particularly following gastric cancer surgery, is linked to increased mortality. The substantial decline in physical activity post-surgery contributes to a notable reduction in cardiorespiratory fitness and lower extremity muscle strength. Early postoperative exercise has demonstrated positive outcomes in colorectal cancer patients, facilitating early hospital discharge and supporting long-term recovery. However, there is a paucity of research on the efficacy of early postoperative exercise in the context of gastric cancer. Therefore, this study aims to evaluate the impact of early postoperative exercise on physical function following gastric cancer surgery.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. Adult men and women 19 years of age or older 2. Pathologically diagnosed gastric cancer 3. Able to undergo radical resection (R0) 4. Scheduled for minimally invasive surgery (MIS) Exclusion Criteria: 1. Pregnant or lactating women 2. Have received chemotherapy and radiation before surgery 3. Scheduled for open surgery 4. Subjects who do not understand or have not given informed consent 5. If healthcare provider (primary care physician) deems it difficult for you to exercise

Gender: All

Minimum age: 19 Years

Maximum age: 80 Years

Healthy volunteers: Accepts Healthy Volunteers

Locations:

Facility:
Name: Department of Surgery, Yonsei University College of Medicine

Address:
City: Seoul
Country: Korea, Republic of

Start date: January 3, 2023

Completion date: April 30, 2024

Lead sponsor:
Agency: Yonsei University
Agency class: Other

Source: Yonsei University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06260293

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