Hypnosis may offer Drug-Free relief for COPD anxiety and breathlessness
NCT ID NCT04868357
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether learning self-hypnosis can help people with severe COPD manage anxiety and shortness of breath during pulmonary rehabilitation. 133 participants took part, with some learning hypnosis techniques in two group sessions. The goal was to see if hypnosis could reduce anxiety and improve breathing comfort, both during rehab and for three months after. If effective, it could provide a simple, complementary tool for symptom relief.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- self-administered hypnosis (behavioral intervention)
- What this could lead to
- If it works, this could give COPD patients a simple, drug-free way to manage anxiety and breathlessness at home.
- What could go wrong
- This is a small, completed trial with 133 participants. Hypnosis may not work for everyone, and benefits might not last long-term.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
133 people
The number who actually took part.
- Started
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Sep 2021
- Finished
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Apr 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
30 to 90 years
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged \> 30. * Affiliated to a Social Security scheme or beneficiary of such a scheme. * Absence of cognitive disease questioning the validity of patient reported outcomes * Ability to give free, informed consent. * Adult patients with severe COPD, dyspnea ; with distension. * Hospitalized at the CHB. * Predicted FEV1 and FEV/FVC percentages consistent with severe COPD according to GOLD standards. * Modified Research Council Questionnaire ≥2 * Exposure to tobbacco \>= 10 packs/yrs. Exclusion Criteria: * Pregnancy * Known severe cardiac insufficiency. * Known severe pulmonary arterial hypertension. * Evolutive-cancer diagnosis. * Significant cognitive impairment, hypercapnic encephalopathy or confusional syndrome. * Deafness. * Anemia ≤ 8g/dL. * Psychotic pathology.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Centre Hospitalier de Bligny
Briis-sous-Forges, Briis-sous-Forges, France, France
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