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Behavior and Knowledges of Patients Enrolled Into SIOUX Study (COM-Patient)

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ClinicalTrials.gov Identifier: NCT02900586
Recruitment Status : Active, not recruiting
First Posted : September 14, 2016
Last Update Posted : April 15, 2019
Sponsor:
Collaborator:
University of Lorraine
Information provided by (Responsible Party):
Centre Hospitalier Régional Metz-Thionville

Brief Summary:
The purpose of this study is to contribute to the evaluation of SIOUX study by adding data about the choices of the observant patients, the mis-observant ones or the protocol deviations.

Condition or disease
Osteoporosis

Detailed Description:
The adherence to treatment for osteoporosis doesn't exceed 50% after one year. The SIOUX project about the inter-professional collaboration (attending physician with dispensary pharmacist) developed therapeutic patient education (TPE) plans and created follow-up booklets which were dealt to the patients who have to transmit it to their two medical professionals twice a year during three years one after one. The results after 18 months are encouraging about the improvement of adherence to treatment and about the lifestyle changes.

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Study Type : Observational
Actual Enrollment : 20 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Understand the Behavior and the Knowledges of Patients Enrolled Into SIOUX Study
Actual Study Start Date : May 2016
Actual Primary Completion Date : November 2017
Estimated Study Completion Date : December 2019



Primary Outcome Measures :
  1. Medication management [ Time Frame: year 1 ]
    semi-structured interview



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Osteoporotic patients who have been enrolled into SIOUX study
Criteria

Inclusion Criteria:

  • patients enrolled into SIOUX study

Exclusion Criteria:

  • cognitive troubles which prevent the patient to participate in individual interview

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02900586


Locations
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France
Hôpital de Mercy - CHR Metz-Thionville
Metz Cedex 03, France, 57085
Sponsors and Collaborators
Centre Hospitalier Régional Metz-Thionville
University of Lorraine
Investigators
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Principal Investigator: Didier POIVRET, MD CHR Metz-Thionville

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Responsible Party: Centre Hospitalier Régional Metz-Thionville
ClinicalTrials.gov Identifier: NCT02900586     History of Changes
Other Study ID Numbers: 2015-01Obs-CHRMT
First Posted: September 14, 2016    Key Record Dates
Last Update Posted: April 15, 2019
Last Verified: April 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Additional relevant MeSH terms:
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Osteoporosis
Bone Diseases, Metabolic
Bone Diseases
Musculoskeletal Diseases
Metabolic Diseases