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

NCT07755917 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 490

Last updated 2026-08-10

No results posted yet for this study

Summary

The goal of this prospective, multicenter, open-label randomized controlled clinical trial is to evaluate whether a home-based, digitally supervised multi-modal prehabilitation intervention can improve functional capacity, treatment tolerance, and short- and long-term clinical outcomes in gastric cancer patients who have completed 2-4 cycles of neoadjuvant chemotherapy and are scheduled for radical gastrectomy.

Conditions

Interventions

BEHAVIORAL

mHealth prehabilitation group

receiving at least 4 weeks of 5G+AI digitally supervised home-based multi-modal prehabilitation plus standard ERAS perioperative management

OTHER

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

  • 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
  • Peking University Cancer Hospital (Inner Mongolia Campus)

    collaborator UNKNOWN
  • The Affiliated Hospital of Qingdao University

    lead OTHER

Principal Investigators

  • Yanbing Zhou · The Affiliated Hospital of Qingdao University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-31
Primary Completion
2028-09-01
Completion
2030-09-01

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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 NCT07755917 on ClinicalTrials.gov