Anticipating and Tracking: Pack of Gerontological Assessment Embedded

Elderly Clinical Trial

— ARPEGE  

Official title:

Anticipating and Tracking: Pack of Gerontological Assessment Embedded

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02818439
• Other study ID #: PO12141
• Status: Active, not recruiting
• Phase: N/A
• First received: June 16, 2016
• Last updated: December 1, 2017
• Start date: October 14, 2013
• Est. completion date: October 2018

Study information

• Verified date: December 2017
• Source: CHU de Reims
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

ARPEGE project fits within the general framework of maintaining functional autonomy in the frail elderly. The early identification of elderly people at risk of frailty is essential to be able to make corrective actions to maintain a quality of life desired by the person. ARPEGE offers tracking and monitoring based on a corpus mobile evaluation of frailty, that could be used in various environments (home, prevention center, office of the general practitioner, geriatric consultation), and manipulated intuitively by professionals not specialists.

This four-year project spearheaded by the University of technology of Troyes in partnership with the University of Reims Champagne-Ardenne also brings a set of partners and experts in the region and outside, so that the proposed solution has the qualities necessary for its deployment in terms of value diagnostic, use, acceptability and perfectly controlled ethics.

The Region has made "longevity aging" theme one of its priorities. This image of driver of innovation in this area can only be enhanced by a program like ARPEGE. Beyond the scientific and technological results expected, one can imagine the potential socio-economic benefits if this tracking solution is deployed on a large scale.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 216
• Est. completion date: October 2018
• Est. primary completion date: October 14, 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 70 Years and older

Eligibility

Inclusion Criteria:

• 70 years or older

• GIR 4, 5 or 6

• Consenting to participate in the study

Exclusion Criteria:

• Severe cognitive impairment ( MMSE < 10)

• Major neurosensory disorders

• Full hospitalization or not (acute care and rehabilitation..)

• Non- affiliation to a social security scheme

• Major protected by law (guardianship, trusteeship)

• Informed consent not provide

Related Conditions & MeSH terms

• Elderly

Intervention

Other:
• evaluation of frailty

Locations

Country	Name	City	State
France	Chu Reims	Reims

Sponsors (1)

Lead Sponsor	Collaborator
CHU de Reims

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Duke Health Profile: Quality of life questionnaire	The Duke Health Profile is a generic health-related quality of life questionnaire that comprises 17 items grouped in 10 scales: physical health, mental health, social health, general health (aggregate score of the 3 previous scales), perceived health, self-esteem, anxiety, depression, pain, and disability.; Scores of each scale range from 0 to 100, with 100 representing optimum quality of life.	up to 36 months