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An mHealth-based intervention to improve prehabilitation and enhanced recovery after surgery in patients with esophageal cancer: a randomized controlled trial

An mHealth-based intervention to improve prehabilitation and enhanced recovery after surgery in patients with esophageal cancer: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045650
Enrollment
Unknown
Registered
2021-04-20
Start date
2021-04-19
Completion date
Unknown
Last updated
2021-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

esophageal cancer

Interventions

Intervention Group:Nutrition guidance + Physical exercise guidance + Stress reduction intervention
Control Group:Routine prehabilitation and postoperative management

Sponsors

Sun Yat-Sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The biopsy pathology of the patient must be diagnosed by a pathologist and confirmed to be esophageal cancer, able to tolerate esophageal cancer resection; 2. Aged 18-75 years, life expectancy> 12 months; 3. Gastrointestinal digestion and absorption are normal before operation; 4. Karnofsky score >= 90 points; 5. Able to walk continuously for more than 6 minutes; 6. Patients or their family members use mobile phone WeChat; 7. The included patients have basic communication and understanding skills, must be informed, understand the study, and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with esophageal cancer with distant metastasis; 2. There are contraindications to physical activity, such as orthopedic diseases, rheumatism, cardiovascular diseases (unstable angina or severe aortic stenosis, etc.), neurological diseases (epilepsy, stroke, Parkinson's disease, muscular dystrophy, etc.); 3. People who are infected and carriers of HIV virus; 4. Female patients during pregnancy and lactation; 5. Those who cannot complete the questionnaire due to mental disorders; 6. No R0 resection; 7. Concomitant with other malignant diseases at the same time.

Design outcomes

Primary

MeasureTime frame
Quality of life;

Secondary

MeasureTime frame
Weight;Physical fitness;Mental health;

Countries

China

Contacts

Public ContactZhang Xu

Sun Yat-Sen University Cancer Center

zhangxu@sysucc.org.cn+86 20 87343317

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026