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Development, Application, and Evaluation of a Mindfulness-Based Intervention Program for Postoperative Lung Cancer Patients

Development, Application, and Evaluation of a Mindfulness-Based Intervention Program for Postoperative Lung Cancer Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080459
Enrollment
Unknown
Registered
2024-01-30
Start date
2024-03-01
Completion date
Unknown
Last updated
2025-04-14

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

Conditions

Postoperative Lung Cancer

Interventions

Experimental Group:An 8-week Mindfulness-Based Intervention Program and Usual Care
Control Group:Usual Care

Sponsors

Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Postoperative patients with Stage I, II, or III lung cancer. 2. Age 18 years or older. 3. Clear consciousness, informed about the diagnosis, and capable of independent communication. 4. Volunteer to participate in the trial and sign an informed consent before the study begins.

Exclusion criteria

Exclusion criteria: 1. Patients who have previously participated in a mindfulness intervention program. 2. Recurrence of lung cancer or metastasis to distant organs. 3. Concurrent treatment with chemotherapy, radiotherapy, immunotherapy, targeted therapy, or other therapeutic modalities. 4. Coexistence of other malignant tumors requiring treatment.

Design outcomes

Primary

MeasureTime frame
Mindful Attention Awareness;—

Secondary

MeasureTime frame
Biomarker;Self-care Ability and Empathy;Negative Emotions;Analogue;Concerns About Recurrence ;sleep quality;—

Countries

China

Contacts

Public ContactYing Zhou

Guangzhou Medical University

zhouying0610@163.com+86 136 6005 1617

Outcome results

None listed

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