Development of the General Scale Observance for Chronic Diseases
EGOMAC
1 other identifier
observational
397
1 country
1
Brief Summary
The main objective is to assess the measurement characteristics (validity, reproducibility) and the invariance of EGOMAC scale in a population of consultants in diabetology, cardiology and rheumatology hospital and liberal and hospital oncology and Infectious disease, by following the evolution of patient compliance at D0 and D15. The second objective is to assess the sensitivity to change of scale EGOMAC following developments compliance 3 months.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2014
Typical duration 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
June 1, 2014
CompletedFirst Submitted
Initial submission to the registry
August 23, 2016
CompletedFirst Posted
Study publicly available on registry
August 31, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2017
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2017
CompletedAugust 16, 2017
August 1, 2017
2.8 years
August 23, 2016
August 13, 2017
Conditions
Outcome Measures
Primary Outcomes (2)
EGOMAC questionnaire
baseline
Change in EGOMAC questionnaire
15 days
Eligibility Criteria
Population of consultants in diabetology, cardiology and rheumatology hospital and liberal and hospital oncology and Infectious disease
You may qualify if:
- patient age of 18 years
- from routine patient counseling
- with at least one of these diseases : heart failure, hypertension, coronary disease, type 2 diabetes, osteoarthritis of the knee or hip, osteoporosis, inflammatory rheumatism (rheumatoid arthritis, spondyloarthropathy), cancer ( with only non-hormonal oral anti cancer treatments) and HIV.
- patient can read the French language in order to complete the self -administered questionnaire
- patient agreeing to participate in the study
You may not qualify if:
- patient receiving no drug prescription or recommendation of lifestyle or diet (for example consultationpurely diagnostic ).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Central hospital
Nancy, 54000, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Francis GUILLEMIN, MD, PhD
CHRU Nancy
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 23, 2016
First Posted
August 31, 2016
Study Start
June 1, 2014
Primary Completion
April 1, 2017
Study Completion
April 1, 2017
Last Updated
August 16, 2017
Record last verified: 2017-08
Data Sharing
- IPD Sharing
- Will share
open to partnership