BPCeaux: The Effect of Spa Treatment on Chronic Obstructive Pulmonary Disease

Sponsor
Centre Hospitalier Universitaire de Nīmes (Other)
Overall Status
Terminated
CT.gov ID
NCT01296854
Collaborator
(none)
39
6
2
37
6.5
0.2

Study Details

Study Description

Brief Summary

The primary objective of this study is to measure and compare the number of exacerbations (moderate or severe) between the two groups of randomized patients with and without thermal treatment). An exacerbation is defined by an increase in symptoms which justifies a unscheduled medical action: increased daily treatment and / or use of corticosteroids, and / or antibiotic therapy. Exacerbations are documented via prescriptions, hospitalisation reports or unscheduled visits.

Condition or Disease Intervention/Treatment Phase
  • Other: Spa therapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
39 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
The Effect of Spa Treatment on Chronic Obstructive Pulmonary Disease
Study Start Date :
May 1, 2011
Actual Primary Completion Date :
Jun 1, 2014
Actual Study Completion Date :
Jun 1, 2014

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Standard

The patients randomized into this arm of the study will not have spa therapy.

Experimental: Spa Therapy

The patients randomized into this arm of the study will have 3 weeks of spa therapy

Other: Spa therapy
3 weeks of spa therapy

Outcome Measures

Primary Outcome Measures

  1. Number of exacerbations [12 months after the beginning of treatment]

    Exacerbation = increase in symptoms (IS) justifying an unprogrammed therapeutic intervention (TI). An IS = increase in >=2 of the following minor symptoms for >= 2 consecutive days (CD): (i) dyspnea, (ii) volume or (iii) purulence of sputum. Or an increase in any 1 of the following major symptoms associated with any of the minor symptoms for at least 2 CD: (a) sore throat, (b) cold, (c) fever, (d) coughing, (e) wheezing. A TI = systemic corticoids and/or antibiotics. An exacerbation is defined as severe if TI is accompanied by a hospital stay > 24h, and as "moderate" otherwise.

Secondary Outcome Measures

  1. change in the BODE score [3 weeks]

  2. change in SF36 questionnaire scores [3 weeks]

    the SF36 quality of life questionnaire

  3. Cost (€) [3 weeks]

    Costs are evaluated from the point of view of payers associated with the pathology.

  4. C reactive protein (mg/l) [3 weeks]

    blood work

  5. Eosiniphil count (thou/ml) [3 weeks]

    blood work

  6. Number of exacerbations [3 weeks]

    Exacerbation = increase in symptoms (IS) justifying an unprogrammed therapeutic intervention (TI). An IS = increase in >=2 of the following minor symptoms for >= 2 consecutive days (CD): (i) dyspnea, (ii) volume or (iii) purulence of sputum. Or an increase in any 1 of the following major symptoms associated with any of the minor symptoms for at least 2 CD: (a) sore throat, (b) cold, (c) fever, (d) coughing, (e) wheezing. A TI = systemic corticoids and/or antibiotics. An exacerbation is defined as severe if TI is accompanied by a hospital stay > 24h, and as "moderate" otherwise.

  7. change in the BODE score [3 months]

  8. change in the BODE score [6 months]

  9. change in the BODE score [9 months]

  10. change in the BODE score [12 months]

  11. change in SF36 questionnaire scores [3 months]

    the SF36 quality of life questionnaire

  12. change in SF36 questionnaire scores [6 months]

    the SF36 quality of life questionnaire

  13. change in SF36 questionnaire scores [9 months]

    the SF36 quality of life questionnaire

  14. change in SF36 questionnaire scores [12 months]

    the SF36 quality of life questionnaire

  15. Cost (€) [3 months]

    Costs are evaluated from the point of view of payers associated with the pathology.

  16. Cost (€) [6 months]

    Costs are evaluated from the point of view of payers associated with the pathology.

  17. Cost (€) [9 months]

    Costs are evaluated from the point of view of payers associated with the pathology.

  18. Cost (€) [12 months]

    Costs are evaluated from the point of view of payers associated with the pathology.

  19. Number of exacerbations [3 months]

    Exacerbation = increase in symptoms (IS) justifying an unprogrammed therapeutic intervention (TI). An IS = increase in >=2 of the following minor symptoms for >= 2 consecutive days (CD): (i) dyspnea, (ii) volume or (iii) purulence of sputum. Or an increase in any 1 of the following major symptoms associated with any of the minor symptoms for at least 2 CD: (a) sore throat, (b) cold, (c) fever, (d) coughing, (e) wheezing. A TI = systemic corticoids and/or antibiotics. An exacerbation is defined as severe if TI is accompanied by a hospital stay > 24h, and as "moderate" otherwise.

  20. Number of exacerbations [6 months]

    Exacerbation = increase in symptoms (IS) justifying an unprogrammed therapeutic intervention (TI). An IS = increase in >=2 of the following minor symptoms for >= 2 consecutive days (CD): (i) dyspnea, (ii) volume or (iii) purulence of sputum. Or an increase in any 1 of the following major symptoms associated with any of the minor symptoms for at least 2 CD: (a) sore throat, (b) cold, (c) fever, (d) coughing, (e) wheezing. A TI = systemic corticoids and/or antibiotics. An exacerbation is defined as severe if TI is accompanied by a hospital stay > 24h, and as "moderate" otherwise.

  21. Number of exacerbations [9 months]

    Exacerbation = increase in symptoms (IS) justifying an unprogrammed therapeutic intervention (TI). An IS = increase in >=2 of the following minor symptoms for >= 2 consecutive days (CD): (i) dyspnea, (ii) volume or (iii) purulence of sputum. Or an increase in any 1 of the following major symptoms associated with any of the minor symptoms for at least 2 CD: (a) sore throat, (b) cold, (c) fever, (d) coughing, (e) wheezing. A TI = systemic corticoids and/or antibiotics. An exacerbation is defined as severe if TI is accompanied by a hospital stay > 24h, and as "moderate" otherwise.

Eligibility Criteria

Criteria

Ages Eligible for Study:
40 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • The patient must have given his/her informed and signed consent

  • The patient must be insured or beneficiary of a health insurance plan

  • The patient must have chronic obstructive pulmonary disease

  • Obstructive ventilation problem: Tiffeneau index (expiratory volume in one second / slow vital capacity) < 70%

  • Expiratory volume in one second < 80% of the theoretical value

  • Reversibility < 12% after inhalation of bronchodilators

  • Smokers or ex smokers

  • Available for study monitoring

  • Has access to diagnostic, medical and therapeutic care according to the best, current criteria (see the recommendations of the French Language Pseumologist Society)

Exclusion Criteria:
  • The patient is participating in another study

  • The patient has participated in another study in the past 12 months

  • The patient is in an exclusion period determined by a previous study

  • The patient is under judicial protection, under tutorship or curatorship

  • The patient refuses to sign the consent

  • It is impossible to correctly inform the patient

  • The patient is in military service (unavailable for monitoring)

  • Patient is on parole or otherwise has their liberty restricted by administrative or judiciary decision

  • The patient is pregnant, or does not have contraception

  • The patient is breastfeeding

  • Patient has neoplastic disease

  • Patient has asthma

  • Patient has another, evolving pulmonary disease (tuberculosis, pulmonary interstitium disease, active or recent pulmonary infection)

  • Patient has a clinical history indicating asthma or another respiratory disease (in particular bronchiectasis, pneumoconiosis and other occupational diseases, history of pulmonary neoplasia, HIV, immunosuppressive therapy including corticosteroids in the long term

  • Patient has respiratory insufficiency

  • Hypereosinophilic patient (the number of polynuclear eosinophils is > 0.5 giga/l; confirmed on 2 hemograms)

  • Recent psychiatric trouble (less than 1 year)

  • Takes illegal drugs

  • Patient does not have pneumological care according to the standards set by the French Language Pneumologist Society

Contacts and Locations

Locations

Site City State Country Postal Code
1 Private practice: Karim Berkani Aix les Bains France 73100
2 Private practice: Jean Hérété Amélie les Bains Palalda France 66110
3 Private practice: Pierre Ethève Briey France 54150
4 Private practice: Marc Bellier Ceret France 66400
5 Private practice: Pierre Olivier Perpignan France 66000
6 Private practice: Muriel Nouvelle Saint Amand les Eaux France 59230

Sponsors and Collaborators

  • Centre Hospitalier Universitaire de Nīmes

Investigators

  • Study Director: Nicolas Molinari, PhD, Centre Hospitalier Universitaire de Nîmes
  • Principal Investigator: Jean Victor Hérété, MD, Amélie les Bains

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre Hospitalier Universitaire de Nīmes
ClinicalTrials.gov Identifier:
NCT01296854
Other Study ID Numbers:
  • LOCAL/2010/NM-02
  • 2010-A00693-36
First Posted:
Feb 16, 2011
Last Update Posted:
Mar 25, 2015
Last Verified:
Mar 1, 2015
Keywords provided by Centre Hospitalier Universitaire de Nīmes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 25, 2015