Memory Problems Perceptions Among Patients and Accompaniers During Diagnosis Process : (REMAD)

Central Hospital, Nancy, France

Status: Unknown

Conditions: Alzheimer Disease; Memory Disorders

Treatments: Behavioral: Psychological questionnaires

Study type: Interventional

Funder types: Other

Identifiers

NCT02299154

2014-A00156-41

Details and patient eligibility

About

This study aims to prospectively examine the memory problem perceptions of patients with memory complaints [MCs] and their accompaniers during the diagnostic process.

Full description

Through the french adaptation of the "illness perception questionnaire memory", this study aims to prospectively examine the memory problem perceptions of patients with memory complaints [MCs] and their accompaniers during the diagnostic process. The investigators plan to recruit 125 patients with MCs who come for the first time at the Research and Resources Memory Center in Nancy, France. Participants have to express MCs and must be free of dementia diagnosis at the first visit. Participants also need to be accompanied by an accompanier and both have to be fluent in French. This study has been approved by our local Ethics Committee (Committee for the Protection of Persons) and the French Health Security Agency. After giving their informed consent, patients and accompaniers are followed up throughout the diagnostic process with three visits : at their first visit, at one month after the first visit, and at six months after the diagnosis disclosure.

Enrollment: 250 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

For patients with memory complaints:

• Age over 18 years
• Have a memory complaints with a QPC score greater than or equal to 3
• Be accompanied by a next of kin
• Folstein MMSE greater than or equal to 15/30
• Have given their written consent after receiving clear and intelligible oral and written information
• Social security coverage

For Accompaniers :

• Age over 18 years
• Consent to participate at the study with the patient
• Have given their written consent after receiving clear and intelligible oral and written information
• Social security coverage
• Be in contact with the patient at least 8 hours per week. It could be physical contact or telephone contact.

Exclusion criteria

For patients with memory complaints:

• Sensory deficit interfering with the completion of the questionnaires
• Level of French insufficient to complete the questionnaires
• Legally protected person
• Diagnosis of neurocognitive disorders already established
• Treatment for Alzheimer Disease
• Refusal or inability to obtain written informed consent form from the patient
• Included in another experimental study at inclusion visit

For Accompaniers:

• Sensory deficit interfering with the completion of the questionnaires
• Level of French insufficient to complete the questionnaires
• Refusal or inability to obtain written informed consent form from the accompanier

Trial design

Primary purpose: Diagnostic

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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250 participants in 2 patient groups

Patient with memory disorders

Experimental group

Description:

psychological questionnaires

Treatment:

Behavioral: Psychological questionnaires

Accompanier

Experimental group

Description:

psychological questionnaires

Treatment:

Behavioral: Psychological questionnaires