Clinical trial · Interventional
Mindfulness-Oriented Respiratory Distress Symptom Intervention for Lung Cancer
Mindfulness-Oriented Respiratory Distress Symptom Intervention for Patients With Lung Cancer: A Feasibility Randomized Controlled Trial
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 18, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260918-000001
Summary
Brief summary (as posted)
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
Conditions (6)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain Activity | — | UNRESOLVED | — |
| Breathlessness | — | UNRESOLVED | — |
| Coughing | — | UNRESOLVED | — |
| Fatigue Symptom | — | UNRESOLVED | — |
| Lung Cancer Patients | — | UNRESOLVED | — |
| Symptom Cluster | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Mindfulness-Oriented Respiratory Distress Symptom Intervention (M-RDSI) | Behavioral | — | UNRESOLVED |
| Usual Care | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Mindfulness-Oriented Respiratory Distress Symptom Intervention (M-RDSI)
- description
- Patients in the M-RDSI group will receive a 6-week intervention, including 1) mindfulness training, such as mindful breathing and relaxation; 2) controlled breathing techniques, cough suppression techniques, acupressure, and exercise; and 3) using mindful breathing, relaxation, and attitudes to orientate the practice of RDSI.
- interventionNames
- Behavioral: Mindfulness-Oriented Respiratory Distress Symptom Intervention (M-RDSI)
- type
- ACTIVE_COMPARATOR
- label
- Usual care
- description
- Usual care will receive health educational booklets and routine follow-ups offered by the oncology nurse in the cancer center that patients with lung cancer usually receive during the same 6 weeks.
- interventionNames
- Other: Usual Care
Primary outcomes (5)
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * HK patients who can understand Cantonese, aged 18 years or older; * A confirmed diagnosis of an 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 impact on daily life from at least two of the three symptoms, where one symptom is breathlessness; * Stability of COPD, if present; * WHO Performance Status of 0-2; * fMRI can be conducted; * Expected lifespan of more than six months. Exclusion Criteria: * Cognitive impairments, severe psychotic symptoms, or other medical conditions that might hinder participation; * Participating in mindfulness or other psychological support interventions or symptom management interventions.
References
Publications (0)
Data not yet available