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Development and Empirical Study of an Intelligent Preoperative Prehabilitation Management System for Neoadjuvant Therapy Patients with Non-Small Cell Lung Cancer Based on Digital Therapeutics

Development and Empirical Study of an Intelligent Preoperative Prehabilitation Management System for Neoadjuvant Therapy Patients with Non-Small Cell Lung Cancer Based on Digital Therapeutics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127520
Enrollment
Unknown
Registered
2026-07-01
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Non-small cell lung cancer

Interventions

experimental group:Digital therapy combined with accelerated recovery care group

Sponsors

The FIrst Affiliated Hospital, College of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. The age range is from 18 years old to 75 years old; 2. Patients who have undergone neoadjuvant treatment for non-small cell lung cancer and are scheduled to undergo radical lung cancer surgeryPatients who have undergone neoadjuvant treatment for non-small cell lung cancer and are scheduled to undergo radical lung cancer surgery; 3. Have the ability to use smart devices and fill out electronic questionnaires; 4. Patients who are conscious, without any reading, communication or cognitive impairments, understand the purpose of this study, and voluntarily participate;

Exclusion criteria

Exclusion criteria: 1.Patients with mental disorders and cognitive impairments; having a history of major diseases, including a history of other malignant tumors within the past 5 years, and a history of angina pectoris, myocardial infarction, or stroke within the past 6 months; 2.Patients who have previously undergone thoracic surgery; 3.Patients who are unable to move due to organic changes such as injuries or diseases, such as severe arthritis, etc; 4.Pregnant and lactating women;

Design outcomes

Primary

MeasureTime frame
pulmonary function;

Secondary

MeasureTime frame
Health Literacy;Symptom Burden Score;Exercise effect;quality of life;Nutrition score;

Countries

China

Contacts

Public ContactJieping Zhang

The FIrst Affiliated Hospital, College of Medicine, Zhejiang University

zjppxwk@zju.edu.cn+86 571 87237537

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026