Status:
UNKNOWN
Memory Problems Perceptions Among Patients and Accompaniers During Diagnosis Process :
Lead Sponsor:
Central Hospital, Nancy, France
Collaborating Sponsors:
France Alzheimer
Laboratoire APEMAC :Maladies chroniques, santé perçue, processus d adaptation, France
Conditions:
Memory Disorders
Alzheimer Disease
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This study aims to prospectively examine the memory problem perceptions of patients with memory complaints \[MCs\] and their accompaniers during the diagnostic process.
Detailed 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 t...
Eligibility Criteria
Inclusion
- 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
- 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
Key Trial Info
Start Date :
December 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
November 1 2017
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT02299154
Start Date
December 1 2014
End Date
November 1 2017
Last Update
March 8 2016
Active Locations (1)
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1
University Hospital of Nancy ,CHU Brabois, France
Vandœuvre-lès-Nancy, France, 54511