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NCT02900586 Clinical Trial

Behavior and Knowledges of Patients Enrolled Into SIOUX Study

Osteoporosis Clinical Trial

— COM-Patient  

Official title:
Understand the Behavior and the Knowledges of Patients Enrolled Into SIOUX Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02900586
Other study ID # 2015-01Obs-CHRMT
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2016
Est. completion date December 2019

Study information
Verified date March 2020
Source Centre Hospitalier Régional Metz-Thionville
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.

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.

Recruitment information / eligibility
Status Completed
Enrollment 20
Est. completion date December 2019
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patients enrolled into SIOUX study

Exclusion Criteria:

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

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
France Hôpital de Mercy - CHR Metz-Thionville Metz Cedex 03

Sponsors (2)
Lead Sponsor Collaborator
Centre Hospitalier Régional Metz-Thionville University of Lorraine

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Medication management semi-structured interview year 1
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