Chronic Obstructive Pulmonary Disease (COPD) Clinical Trials

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Effectiveness of Hypnosis on Breathlessness Mastery in Patients With Persistent Dyspnea: a Randomised Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Persistent dyspnea is a debilitating symptom, that is common and difficult to treat. This symptom is found in many different diseases including chronic obstructive pulmonary disease (COPD), interstitial lung disease (ILD), chronic heart failure (CHF), and metastatic cancer. Dyspnea is associated with many other symptoms, including anxiety, depression, and fatigue and is responsible for a significant reduction in quality of life. To date, only opiates are recommended for the pharmacological treatment of persistent dyspnea. The effectiveness of hypnosis is well known in the treatment of anxiety and delivered to patients suffering from chronic dyspnea for this reason. One randomised controlled study has shown that a single 20-minute mindfulness sessions could significantly reduce general symptom burden and have a significant impact on anxiety and depression in palliative care patients. Furthermore, the intervention had no negative side effects. Our aim is to evaluate the effectiveness of three hypnosis sessions on breathlessness mastery in patients with persistent dyspnea, using as a primary outcome the mastery domain of a validated tool, the Chronic Respiratory Questionnaire (CRQ).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients aged ≥ 18 years and

• Primary diagnosis of metastatic cancer, COPD stage at least B or E, ILD, or CHF and

• Dyspnea stage NYHA ≥ II or mMRC ≥ 2

Locations
Other Locations
Switzerland
Geneva University Hospitals
RECRUITING
Geneva
Contact Information
Primary
Lisa Hentsch, Dr med
lisa.hentsch@hug.ch
+41 22 305 66 12
Backup
Federica Bianchi, PhD
lisa.hentsch@hug.ch
Time Frame
Start Date: 2026-04-01
Estimated Completion Date: 2028-04-01
Participants
Target number of participants: 82
Treatments
Experimental: Hypnosis
3 hypnosis sessions separated by 15 days
No_intervention: Usual Care
Usual care
Sponsors
Leads: University Hospital, Geneva
Collaborators: Lancardis Foundation

This content was sourced from clinicaltrials.gov