Personalized health plans tested to boost Well-Being in frail seniors
NCT ID NCT06560723
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a personalized health plan (PHP) can improve quality of life for frail people aged 70 and older. Researchers will give participants various quality-of-life tests and share the results with their doctor and the patient. The study will follow 120 participants for two years, comparing those who get the PHP to those who receive usual care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Personalized health plan (PHP) with quality-of-life assessments
- What this could lead to
- If it works, this could show that a personalized health plan helps frail older adults maintain a better quality of life and stay independent longer.
- What could go wrong
- This is a small, early-stage study (120 people) that only measures quality-of-life scores, not hard medical outcomes. Results may not apply to all elderly populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 120 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2030
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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70 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient ≥ 70 years * Autonomous patient (ADL ≥ 5) * Patient identified as frail according to the Gérontopôle de Toulouse GFST grid * Patient whose primary care physician is in the MSPs of Charleval or Romilly sur Andelle for the intervention group, and in the MSPs of Gaillon and Pont de l'Arche for the control group. * Patient living at home or in an RPA * Understanding of the French language * Patient having read and understood the information letter and signed the consent form * Affiliation with a social security scheme Exclusion Criteria: * Hospital geriatric follow-up * Geriatric assessment already carried out * Person deprived of liberty by an administrative or judicial decision, or placed under court protection / sub-guardianship or curatorship * History of illness or psychological or sensory abnormality likely to prevent the subject from fully understanding the conditions required for participation in the protocol, or from giving informed consent.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
4 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Charleval
Charleval, 27380, France
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GAILLON
Gaillon, 27600, France
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Pont de L'Arche
Pont-de-l'Arche, 27340, France
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Romilly Sur Andelle
Romilly-sur-Andelle, 27610, France