A Three-Point message could boost medication adherence in chronic disease
NCT ID NCT06748118
First seen Jul 01, 2026 · Last updated Jul 02, 2026 · Updated 1 time
Summary
This study tests whether a simple, standardized, and repeated message from healthcare professionals can improve how well patients with chronic diseases follow their treatment plans. About 1,200 adults with chronic conditions will receive this message during regular consultations. The goal is to see if this approach increases the percentage of patients who take their medications as prescribed.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- simple, standardized, redundant 3-point message delivered by healthcare professionals
- What this could lead to
- If it works, this approach could offer a low-cost way to help many patients with chronic conditions take their medications as prescribed, improving health outcomes.
- What could go wrong
- The message is simple and may not be enough to change long-term habits. Results depend on how consistently healthcare professionals deliver it.
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 1,210 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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Mar 2028
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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18 years and older
- 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: * Adult patients (age ≥ 18 years) * Affiliated to the French social security system * Followed in hospital for a chronic pathology within a formalized care pathway * Having signed a consent form to participate in the study. Exclusion Criteria: * Patients included in the control period. * Patients under guardianship. * Pregnant or breast-feeding patients. * Patients taking part in research on compliance
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Conditions
The condition(s) this trial relates to.
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
10 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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CH d'Antibes
RECRUITINGAntibes, France, 06606, France
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CHU d'Angers
RECRUITINGAngers, France, 49933, France
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CHU de Nantes
RECRUITINGNantes, France, 44000, France
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CHU de Toulouse
RECRUITINGToulouse, France, 31059, France
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CHU de Tours
RECRUITINGTours, France, 37000, France
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Hôpital Bicêtre
RECRUITINGParis, France, 94270, France
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Hôpital Corentin Celton
RECRUITINGIssy-les-Moulineaux, France, 92133, France
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Hôpital La Timone
RECRUITINGMarseille, France, 13005, France
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Hôpital de la Conception
RECRUITINGMarseille, France, 13005, France
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Hôpital européen Georges-Pompidou
RECRUITINGParis, France, 75015, France
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