Not Yet RecruitingNot Applicable

Effects of a Visual Interactive LINE Chatbot on Self-Management of EGFR-TKI Related Side Effects in Patients With Lung Cancer

178 participantsStarted 2026-07-01

Plain-language summary

This study aims to evaluate a visual interactive LINE chatbot designed to support self-management of treatment-related side effects among patients with advanced lung cancer receiving epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) therapy. Patients receiving EGFR-TKI treatment often experience long-term side effects that require ongoing self-management. In this randomized controlled trial, participants will be assigned to receive either usual care alone or usual care plus access to the LINE chatbot intervention, which provides visualized and interactive educational content for symptom monitoring and self-care. The primary outcome of this study is self-management ability related to EGFR-TKI-associated side effects. Secondary outcomes include quality of life during treatment and overall satisfaction with the LINE chatbot intervention.

Who can participate

Age range18 Years

SexALL

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Inclusion Criteria: * Patients with newly diagnosed stage IIIB to IVB unresectable or inoperable non-small cell lung cancer (NSCLC), or those with first disease recurrence who are receiving oral targeted therapy. * Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2, with the ability to perform self-care activities. * Patients receiving epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) therapy, including gefitinib, erlotinib, afatinib, dacomitinib, or osimertinib. * Willingness to participate in the study, with completion of the informed consent process and provision of written informed consent. * Ability to communicate in Chinese and to independently operate a smartphone and use the LINE application. Exclusion Criteria: * Patients diagnosed with a second primary malignancy or multiple malignancies. * Patients receiving other anticancer treatments.

What they're measuring

Self-Management Ability（PAM-13）

Timeframe: at baseline and at 1, 3, and 6 months post-intervention

Trial details

NCT IDNCT07310589

SponsorNational Taiwan University Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-12-31

Contact for this trial

LING-SIN HSU, MSN

+886-2-23123456 a109700@ntuh.gov.tw

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