Chronic Pain Clinical Trial
— QOLPainOfficial title:
Observational Study of the Quality of Life for the Chronic Pain Patients Included in a Therapeutic Education Program Focused on Relaxation Techniques
NCT number | NCT04536155 |
Other study ID # | CHMS19002 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | January 2, 2020 |
Est. completion date | October 2, 2023 |
The benefit of learning psychocorporal techniques in Therapeutic Education on the quality of life of patients with chronic pain will be studied. The purpose of this nursing research protocol is to highlight the improvement of the quality of life of chronic pain patients through psycho-physical techniques performed during group therapeutic education workshops.
Status | Recruiting |
Enrollment | 72 |
Est. completion date | October 2, 2023 |
Est. primary completion date | October 2, 2022 |
Accepts healthy volunteers | |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - chronic pain since more the 3months - Patients for whom a group "relaxation techniques" program is planned and accepted by the patient Exclusion Criteria: - Patient with progressive cancer pain - severe psychiatric pathology (example: psychosis, deep melancholy) - Patient not compliant or refusing to participate in research - Person who does not understand French, or illiterate - Person physically unable to complete questionnaires (visually impaired or blind) - Person protected by sections L1121-5 to L1121-8.1 of the French Public Health Code |
Country | Name | City | State |
---|---|---|---|
France | CH Metropole Savoie | Chambéry |
Lead Sponsor | Collaborator |
---|---|
Centre Hospitalier Metropole Savoie |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | change of quality of life during the program | SF36 score | score at the end of the workshop compared to the score at the beginning | |
Secondary | Change in quality of life | assessed by sf36 score | Comparison between the beginning of the program and twelve months after the end of the program. | |
Secondary | Change in anxiety and depression | assessed by HADS | Comparison at different moments in time - beginning, end, 6 months after, 12 months after | |
Secondary | Change in perceived pain | assessed by numeric pain scale | Assessment at the beginning of the program and 12 months after the end using a numerical pain scale | |
Secondary | Evolution in patient's acceptance of chronic pain:after the end | assessed by Chronic Pain Acceptance Questionnaire | Comparison at different moments in time - beginning, end, 6 months after, 12 months after | |
Secondary | Change in physical activity | assessed by SF36 Physical Activity Sub-Scale | Change in physical activity between the beginning of the program and 12 months after the end |
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