Home-based Whole Course Multimodal Prehabilitation Based on 5G + Artificial Intelligence Mobile Health

NCT07764523 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 328

Last updated 2026-08-14

No results posted yet for this study

Summary

The whole course management of gastric caner patients receiving neoadjuvant therapy frequently hinders by challenges such as inaccurate exercise plans, inadequate nutritional supplementary, limited access to timely psychological support, the toxicity of chemtherapy and poor adherence to prehabilitation protocols. AI (Agent Intelligence) have already been demonstrated remarkable capabilities in personalized patient education and improving compliance to perhabilitation protocols. To date, high quality evidence from randomized clinical trials investigating the clinical and oncological benefit of prehabilitation based on 5G+AI mobile health for this patient cohort is lacking.

Conditions

Interventions

BEHAVIORAL

mHealth prehabilitation group

Participants allocated to the intervention group will receive a whole-course, remotely supervised, home-based multimodal prehabilitation programme delivered through a 5G- and artificial intelligence (AI)-enabled digital health platform. The multimodal prehabilitation included physical and respiratory training, nutritional support, and psychosocial treatment. Our center's prehabilitation experts, clinical nutritionists, psychiatrists, surgeons, nurses and oncologists will collaboratively assess and develop prehabilitation plans. The prehabilitation group received a mobile mini-app that provided an exercise program, dietary advice and psychological assessment and intervention. The management of prehabilitation group was carried out in accordance with the standard ERAS protocol from admission until 30 days postdischarge. The ERAS program mainly included malnutrition screening, health education, surgical risk assessment, and smoking and drinking cessation.

BEHAVIORAL

ERAS group

The management of ERAS group was carried out in accordance with the standard ERAS protocol from admission until 30 days postdischarge. The ERAS program mainly included malnutrition screening, health education, surgical risk assessment, and smoking and drinking cessation.

Sponsors & Collaborators

  • Peking University Cancer Hospital (Inner Mongolia Campus)

    collaborator UNKNOWN
  • People's Hospital of Xinjiang Uygur Autonomous Region

    collaborator OTHER
  • First Affiliated Hospital, Sun Yat-Sen University

    collaborator OTHER
  • Sixth Affiliated Hospital, Sun Yat-sen University

    collaborator OTHER
  • Shandong Provincial Hospital

    collaborator OTHER_GOV
  • The Second Hospital of Shandong University

    collaborator OTHER
  • Yantai Yuhuangding Hospital

    collaborator OTHER
  • The Affiliated Hospital of Shandong Second Medical University

    collaborator UNKNOWN
  • Weifang People's Hospital

    collaborator OTHER
  • Shandong Cancer Hospital and Institute

    collaborator OTHER
  • Dongying People's Hospital

    collaborator OTHER
  • Rizhao People's Hospital

    collaborator OTHER
  • Jining First People's Hospital

    collaborator OTHER
  • The Affiliated Hospital of Qingdao University

    lead OTHER

Principal Investigators

  • Yanbing Zhou, MD · The Affiliated Hospital of Qingdao University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-01
Primary Completion
2028-05-30
Completion
2030-05-30

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07764523 on ClinicalTrials.gov