Hyperventilation Clinical Trial
— SHVOfficial title:
Effects of Chest Physiotherapy in Hyperventilation Syndrom : a Multicentric Observational Study
Verified date | August 2023 |
Source | Centre Hospitalier des Pays de Morlaix |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Hyperventilation syndrome induce dyspnea and altered quality of life. the aim of this study is to assess the impact of chest physiotherapy on hyperventilation syndrome' symptoms
Status | Completed |
Enrollment | 46 |
Est. completion date | August 1, 2023 |
Est. primary completion date | August 1, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - patients addressed for hyperventilation syndrome - patient aged 18 years or over - patient able to consent and having sign a consent form Exclusion Criteria: - respiratory disease (COPD, interstitial lung disease, bronchiectasis, cystic fibrosis, uncontrolled asthma) - patient with an inability to complete questionaires - refusal of participation - patient under tutorship or curatorship |
Country | Name | City | State |
---|---|---|---|
France | BEAUMONT | Morlaix |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier des Pays de Morlaix |
France,
Chenivesse C, Similowski T, Bautin N, Fournier C, Robin S, Wallaert B, Perez T. Severely impaired health-related quality of life in chronic hyperventilation patients: exploratory data. Respir Med. 2014 Mar;108(3):517-23. doi: 10.1016/j.rmed.2013.10.024. Epub 2013 Nov 7. — View Citation
Kiesel K, Burklow M, Garner MB, Hayden J, Hermann AJ, Kingshott E, McCullough G, Ricard R, Stubblefield G, Volz J, Waskiewicz D, Englert A. EXERCISE INTERVENTION FOR INDIVIDUALS WITH DYSFUNCTIONAL BREATHING: A MATCHED CONTROLLED TRIAL. Int J Sports Phys Ther. 2020 Feb;15(1):114-125. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change of Nijmegen score | Nijmegen score is measured at baseline and after 5 weeks. The Nijmegen questionnaire allows to assess hyperventilation symptoms. the minimum and maximum values are between 0 to 64, and higher scores mean a worse outcome. | 5 weeks | |
Secondary | change of Nijmegen Score | Nijemegen score is measured at baseline and after 1 week. The Nijmegen questionnaire allows to assess hyperventilation symptoms the minimum and maximum values are between 0 to 64, and higher scores mean a worse outcome. | 1 week | |
Secondary | change of Hospital Anxiety and Depression score (HAD) | Anxiety and depression scores are measured at baseline and after 5 weeks. the minimum and maximum values are between 0 to 21 for each item (Anxiety and Depression), and higher scores mean a worse outcome. | 5 weeks | |
Secondary | change of Short Form-36 score (SF-36) | SF 36 score is measured at baseline and after 5 weeks. SF36 allows to assess quality of life.
the minimum and maximum values are between 0 to 100, and higher scores mean a better outcome. |
5 weeks | |
Secondary | change of Dyspnea-12 score | Dyspnea-12 is measured at at baseline and after 5 weeks.
Dyspnea-12 questionnaire allows to assess sensorial and emotional component of dyspnea. The minimum and maximum values are between à to 36, and higher scores mean a worse outcome. |
5 weeks |
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