Physician-Pharmacist Collaboration for Osteoporotic Patient Follow-up
SIOUX
Assessment of the Follow-up of Osteoporotic Patients by a Physician-pharmacist Collaboration
1 other identifier
observational
120
1 country
1
Brief Summary
The purpose of this study is to evaluate the follow-up of the osteoporotic patient by a physician-pharmacist collaboration.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2013
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2013
CompletedFirst Submitted
Initial submission to the registry
August 26, 2016
CompletedFirst Posted
Study publicly available on registry
September 8, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
February 1, 2019
CompletedJanuary 2, 2020
December 1, 2019
6 years
August 26, 2016
December 31, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Respect of treatment and of hygienic dietary measures by patients with a self-questionnaire per medical check
This assessment will be made at the end of the follow-up, after three years, but an intermediary assessment about those same criteria is planned at one and two years of the follow-up.
year 3
Secondary Outcomes (2)
Qualitative evaluation of the professional adhesion for the follow-up process once a year during the annual meeting
year 3
Quantitative evaluation of it by the return rate of questionnaires
year 3
Eligibility Criteria
Patient having osteoporosis enrolled into the programm of Therapeutical Educational for patient
You may qualify if:
- older than 18 years old
- having an osteoporosis treatment
- following a Therapeutical Education for Patient
You may not qualify if:
- opposition for anonymised data gathering
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHR Metz-Thionville
Metz, 57085, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Didier POIVRET, MD
CHR Metz-Thionville
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 26, 2016
First Posted
September 8, 2016
Study Start
January 1, 2013
Primary Completion
January 1, 2019
Study Completion
February 1, 2019
Last Updated
January 2, 2020
Record last verified: 2019-12
Data Sharing
- IPD Sharing
- Will not share