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Teaming up for heart health: new study explores Patient-Caregiver collaboration in mental illness

NCT ID NCT03689296

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at how people with long-term mental disorders and their caregivers can work together to improve heart health. People with these conditions often die 20 years earlier than others, mainly from heart disease. The researchers interviewed 127 participants to understand their experiences and ideas, aiming to find better ways to reduce heart risks.

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.

Participants

127 people

The number who actually took part.

Started

Jun 2019

Finished

Aug 2024

Lead sponsor

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.

Who is studied

Patients followed in ambulatory or full hospitalization (depending study phase)

Ages

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: 1. For all groups: * Adult person, * Person who has given his or her consent to participate in the study, with the consent of the tutor in the context of guardianship, * Fluent use of the French language, 2. For the "Users" group: \- Person with a long-term psychological disorder: Long-term illness (ALD 23), followed by outpatient or full hospitalization 3. For the "Caregivers" group: \- Adult helping a person with a long-term psychological disorder with a Long-Term Disability (ALD 23) and who has given his or her consent to be contacted for the study, 4. For the "Primary Care Professionals" group: \- Primary care professional in practice following at least one person with a long-term psychological disorder with a Long-Term Disability (ALD 23), 5. For the "Psychiatric Professionals" group - Professional currently in practice who is part of a psychiatry team or in private practice Exclusion Criteria: 1\. For all groups: * Person who is physically or psychologically unable to participate in the focus group and/or program at the time of the study * Person not affiliated to the National Health Insurance * Objection to participation by the patient or his legal representative, carers and health professionals. * Patient under guardianship * Patient who participated in Phase 1 or 2 of the study * Patient not able to attend the 6-month visit

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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.

Contacts and locations

Locations

  • Chu Dijon Bourogne

    Dijon, 21000, France