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Development of an Intelligent Preoperative Prehabilitation Management Protocol for Patients Undergoing Neoadjuvant Therapy in Non-Small Cell Lung Cancer Based on Digital Therapeutics

Development of an Intelligent Preoperative Prehabilitation Management Protocol for Patients Undergoing Neoadjuvant Therapy in Non-Small Cell Lung Cancer Based on Digital Therapeutics

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122018
Enrollment
Unknown
Registered
2026-04-08
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-14

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
Nutrition score;Exercise effect;pulmonary function;

Secondary

MeasureTime frame
Symptom Burden Score;Health Literacy;quality of life;

Countries

China

Contacts

Public ContactJieping Zhang

The FIrst Affiliated Hospital, College of Medicine, Zhejiang University

zjppxwk@zju.edu.cn+86 571 8723 7537

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026