Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07281300

Mindfulness-Oriented Respiratory Distress Symptom Intervention for Lung Cancer

Led by The Hong Kong Polytechnic University · Updated on 2026-04-17

64

Participants Needed

1

Research Sites

102 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lung cancer is the leading cause of cancer mortality, posing a critical public health challenge in both Hong Kong and global populations. Patients with lung cancer frequently experience a distressing symptom cluster characterized by breathlessness-driven respiratory distress, accompanied by persistent cough and fatigue, which collectively impose a substantial disease burden. While our research team leader previously developed and validated a multi-component Respiratory Distress Symptom Intervention (RDSI) in England, demonstrating clinical efficacy for lung cancer management, its impact on psychological distress (anxiety and depression) proved limited. This limitation may reflect insufficient integration of psychological components, a crucial consideration given the well-established bidirectional relationship between respiratory symptoms and psychological distress. Emerging evidence indicates that mindfulness interventions provide dual therapeutic benefits by improving patient adherence and effectively addressing both physical symptoms, such as breathlessness and fatigue, as well as psychological distress, including anxiety and depression. Meanwhile, current evaluation methodologies have mainly focused on behavioral data collection, such as self-reported questionnaires, to reflect the effect before and after the intervention. Neuroimaging data can help understand the brain mechanisms underlying breathlessness and elucidate the effectiveness of interventions, thereby improving intervention strategies.

CONDITIONS

Official Title

Mindfulness-Oriented Respiratory Distress Symptom Intervention for Lung Cancer

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Hong Kong patients who understand Cantonese and are aged 18 years or older
  • Confirmed diagnosis of intrathoracic malignancy including small cell lung cancer, non-small cell lung cancer, or mesothelioma
  • At any stage of cancer treatment or palliative care
  • Self-reported daily life impact from at least two symptoms, one being breathlessness
  • Stable COPD if present
  • WHO Performance Status of 0 to 2
  • Able to undergo fMRI scans
  • Expected lifespan longer than six months
Not Eligible

You will not qualify if you...

  • Cognitive impairments, severe psychotic symptoms, or other medical conditions that may interfere with participation
  • Currently participating in mindfulness, psychological support, or other symptom management interventions

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

The Hong Kong Polytechnic University

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

Y

Yan LI

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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