Quality of life assessment for gastric cancer survivors using a smartphone app
A Multi-center, Prospective, Randomized Study to Evaluate the Usefulness of Applying the Chronic Side Effect Management Platform (Wecare) in Gastric Cancer Survivors
This study tests if a smartphone app can help improve the quality of life for gastric cancer survivors after surgery compared to standard care.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 88 (estimated) |
| Ages | 19 Years to 75 Years |
| Sex | All |
| Sponsor | Gyeongsang National University Hospital Academic / other |
| Locations | 1 site (Changwon, Gyeongsandnam-do) |
| Trial ID | NCT06395935 on ClinicalTrials.gov |
What this trial studies
This study evaluates the impact of a smartphone application, Wecare, on the quality of life of gastric cancer survivors who have undergone gastrectomy. It utilizes the KOQUSS-40 method to assess quality of life and compares outcomes between patients using the app and those receiving standard care. The study aims to address the various physical and psychological challenges faced by these patients post-surgery. By leveraging technology, the study seeks to enhance recovery and overall well-being in this population.
Who should consider this trial
Good fit: Ideal candidates are adults aged 19-75 who have undergone radical gastrectomy for gastric cancer.
Not a fit: Patients who cannot participate in regular follow-up or lack communication skills may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve the quality of life for gastric cancer survivors through enhanced support and management of post-surgical symptoms.
How similar studies have performed: While other studies have shown success with smartphone-based interventions in cancer care, this specific approach for gastric cancer survivors is novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Adult patient (19-75 years) who underwent radical gastrectomy Exclusion Criteria: * Patients who were unable to undergo regular follow-up, lacked communication, or were deemed unsuitable to participate in this study by the researcher
Where this trial is running
Changwon, Gyeongsandnam-do
- Gyeongsang National University Hospital — Changwon, Gyeongsandnam-do, South Korea (Recruiting)
Study contacts
- Principal investigator: Sang-Ho Jeong, MD — Gyeongsang National University Changwon Hospital
- Study coordinator: Sook-Ran Park
- Email: sr0218@naver.com
- Phone: +82552142318
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.