Quality of Life and Behavioral Change of Retired Persons (R-FORM')

Pasteur Institute of Lille (IPL)

Status: Completed

Conditions: Healthy Volunteers

Treatments: Other: Group nutrition and physical activity coaching; Other: Group cognition coaching

Study type: Interventional

Funder types: Other

Identifiers

NCT06432010

2021-A00408-33

Details and patient eligibility

About

Researchers have found that the first phase of aging, called "frailty", is insidious, silent and slowly progressive. It begins well before the first signs of aging and possibly before retirement age with physiological reserves that are gradually depleted. Frailty is multifactorial. It is situated between the "robust-vigorous" and "poly-pathological-dependent" stages of aging. This state remains dynamic and above all reversible through screening and awareness of the individual's health determinants as well as motivation to change.

The Longevity Pathway was designed to meet several concrete objectives ranging from improving prevention to advancing research on the topic of longevity and aging well.

This study aims to evaluate the effect of this personalized support on the quality of life of the consultants, but also on many health parameters, 12 months after the end of the proposed coaching.

Full description

The study will be carried out on healthy volunteers, retired.

The main objective of the study is to evaluate the effect of a health check-up followed by a collective "coaching" type of support on the quality of life of retired people 12 months after the end of the coaching sessions.

Enrollment: 100 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Man or Woman;
• Retired;
• Having the desire to change his/her lifestyle;
• Agreeing to follow the constraints generated by the study (presence during the coaching sessions and the final assessment).
• Having signed the informed consent form;
• Social insured;

Exclusion criteria

• Presenting a pathology requiring a complementary assessment and/or the implementation of a treatment that could prevent the realization of the coaching or that could modify its effect;
• Subject participating in another clinical study or in period of exclusion from another study;
• Subject deprived of liberty;
• Subject under judicial protection measure;
• Whose main investigator or a qualified co-investigator judges that the state of health or the concomitant treatments are not compatible with the good progress of the clinical study;.

Trial design

Primary purpose: Prevention

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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100 participants in 3 patient groups

Group nutrition and physical activity coaching

Other group

Description:

Initial health check-up → 7 weeks nutrition and physical activity coaching → 2 telephone follow-ups at 3 and 6 months after → Final health check-up (12 months after)

Treatment:

Other: Group nutrition and physical activity coaching

Group cognition coaching

Other group

Description:

Initial health check-up → 7 weeks cognition coaching → 2 telephone follow-ups at 3 and 6 months after → Final health check-up (12 months after)

Treatment:

Other: Group cognition coaching

control group

No Intervention group

Description:

The study is controlled by the presence of a control group (non-coaching group). 25 people will be included in the control group. They will only benefit from the initial and final health check-up.