Effectiveness of the Jeanne et Léon Program® on the Residents's Frailty in Temporary

Launched by JEANNE ET LEON DEVELOPPEMENT · Dec 19, 2022

Keywords

ClinConnect Summary

This clinical trial is studying the effectiveness of the Jeanne et Léon Program® in helping elderly residents who are temporarily staying in a care facility. The program aims to improve their overall well-being and reduce frailty, which is a condition that can make it harder for older adults to stay active and healthy. The program includes various activities that focus on physical health, nutrition, social interaction, and mental well-being. By participating in these activities, residents may see improvements that last even after the program ends.

To be eligible for this trial, participants need to be 60 years or older and have been living in the temporary accommodation for no more than 72 hours. They should also be able to understand and communicate in French and agree to follow the program for up to six months after their stay. Participants can expect to engage in stimulating activities that are designed to help them stay active and connected with others. It's important to note that those with certain medical issues or communication difficulties may not be able to participate.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Aged 60 years and over
• • Participant who has been living in temporary accommodation at the Résidence Les Tamaris for a maximum of 72 hours
• • Visual, auditory and oral or written abilities in French sufficient to complete the assessments and participate in the Jeanne \& Léon® Program activities
• • Agrees to participate in the study and follow-ups for up to six months after the end of the activity program/temporary residence
• • Non-opposition accompanied by the information note co-signed by the investigator and the resident participating in the study, or the family member or the designated trusted person (if applicable)
• • Must be affiliated to a social security plan
• Exclusion Criteria:
• • Refusal to participate by the resident, family member or designated support person
• • Communication difficulties, sensory and/or motor deficits
• • Medical contraindication
• • Participant already included in another research protocol
• • Person under legal protection

Trial Officials