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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