Early Postoperative Intervention in Gastric Cancer Patients

NCT07444099 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 264

Last updated 2026-03-02

No results posted yet for this study

Summary

This study was conducted by Qilu Hospital and five other renowned medical centers, aiming to evaluate the impact of early structured postoperative intervention on quality of life and prognosis in patients with gastric cancer after neoadjuvant therapy.

Conditions

  • Gastric Cancer (GC)
  • Postoperative Recovery

Interventions

COMBINATION_PRODUCT

Early structured postoperative intervention encompassing nutrition, psychology, and exercise

Nutritional intervention: Routine postoperative oral nutritional supplements (ONS) will be provided, and patients with metabolic diseases such as diabetes will undergo strict glycemic control. Psychological intervention: Patients with a Hospital Anxiety and Depression Scale (HADS) score ≥ 8 will receive cognitive behavioral therapy (CBT), and those with a HADS score ≥ 11 will be referred for psychological consultation. Exercise intervention: Postoperative rehabilitation training will be guided according to different postoperative periods.

Sponsors & Collaborators

  • Linyi People's Hospital

    collaborator OTHER
  • Liaocheng People's Hospital

    collaborator OTHER
  • Yantai Yuhuangding Hospital

    collaborator OTHER
  • Central Hospital of Zibo

    collaborator OTHER
  • Weifang People's Hospital

    collaborator OTHER
  • Qilu Hospital of Shandong University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-10
Primary Completion
2027-03-10
Completion
2027-06-30

Countries

  • China

Study Locations

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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 NCT07444099 on ClinicalTrials.gov