Healthy Aging Together - "Getting to Know You Better": Healthy Aging and Predictive Indicator
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Health assessment.
- Who it may be relevant to
- Registry conditions: Aging Disorder. Basic parameters: from 55 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
A key challenge lies in preventing the loss of autonomy and promoting healthy aging-a concept now widely addressed through multidimensional and multidisciplinary approaches, as evidenced by frailty models, comprehensive geriatric assessment practices, and the WHO's "intrinsic capacity" model. That said, there is a need to assess in greater detail the extent to which individual factors contribute to health trajectories and to move further by adopting a systemic approach that examines not only the relationships between variables but also their complex interactions. The aim of this study is to identify the multidimensional determinants (medical, physical, nutritional, sensory, psycho-cognitive, psychosocial, and socioeconomic) associated with the autonomy and quality of life of older adults and those who are aging.
Interventions
- Other Health assessment
Questionnaires and tests on health behaviors and health
Primary outcome measures
- assessment of Autonomy [Time frame: at baseline, 6 months later and 12 months later]
Secondary outcome measures (10)
- Quality of life [Time frame: at baseline, 6 months later and 12 months later]
- Daily Physical activity Practice (physical behavioral lifestyle measure [Time frame: at baseline, 6 months later and 12 months later]
- Sarcopenia (physical measure) [Time frame: at baseline, 6 months later and 12 months later]
- Physical functional force (physical measure) [Time frame: at baseline, 6 months later and 12 months later]
- Eating habits (nutritional behavioral lifestyle measure [Time frame: at baseline, 6 months later and 12 months later]
- Body Mass Index (nutritional measure) [Time frame: at baseline, 6 months later and 12 months later]
- Subjective cognitive complaint (cognitive measure) [Time frame: at baseline, 6 months later and 12 months later]
- Working memory (cognitive measure) [Time frame: : at baseline, 6 months later and 12 months later]
- Psychological quality (psychological measure) [Time frame: at baseline, 6 months later and 12 months later]
- Locus of Control (psycho-social measure) [Time frame: at baseline, 6 months later and 12 months later]
Eligibility criteria
Inclusion criteria
- Age 55 years or older
- Affiliation with or beneficiary of a social security scheme
- No objection to the study
Exclusion criteria
- Persons protected by law, under guardianship or curatorship,
- Persons deprived of liberty
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07734246 · 25-PP-30