- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04342520
Anxiety Related to the Diagnosis of Alzheimer's Disease or Related Diseases (ADIMA)
Improving the diagnosis of neurocognitive disorders is a major public health challenge. This diagnosis occurs too late in the majority of cases, or is even sometimes non-existent for some despite the presence of clinical signs and symptoms. However, the etiological diagnosis of a TNC is crucial for the patient and his family to understand the most appropriate decisions for the future, to plan the organization of his life as long as he is able to do so, to access the clinical research, to promote dialogue between patients and their caregivers. On the contrary, a late diagnosis may be responsible for the fact that the patient and his / her family are less able to benefit from certain psychosocial interventions, services and treatments.
But the diagnostic announcement is retained. One of the negative and dreaded effects of such an announcement is the negative psychological impact. Some studies show that the diagnostic announcement would worsen the level of anxiety or depressed mood and the risk of social isolation. On the other hand, other studies show that symptoms such as anxiety, psychic distress and depression remain stable, or even decrease slightly after the announcement of the diagnosis, in patients and their relatives. However, the literature is questionable because the majority of the studies are retrospective, mono-centric, and the patient numbers are low. While the first reactions of patients may be negative after the announcement, some report resignation experiences, or form of relief, because they have finally found a clinical explanation for the symptoms encountered. While doubt or diagnostic uncertainty, as well as the feeling of not knowing the truth, seem to have a more damaging psychological impact on the patient and those around him, increasing anxiety and confusion.
The primary objective is to study if the level of anxiety 2 months after the announcement of the diagnosis of Alzheimer's disease or a related disease is not superior to the level of anxiety before the announcement with patient / caregiver.
This present study aim to explore the feasibility with 14 patients.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Improving the diagnosis of neurocognitive disorders is a major public health challenge. This diagnosis occurs too late in the majority of cases, or is even sometimes non-existent for some despite the presence of clinical signs and symptoms. However, the etiological diagnosis of a TNC is crucial for the patient and his family to understand the most appropriate decisions for the future, to plan the organization of his life as long as he is able to do so, to access the clinical research, to promote dialogue between patients and their caregivers. On the contrary, a late diagnosis may be responsible for the fact that the patient and his / her family are less able to benefit from certain psychosocial interventions, services and treatments.
But the diagnostic announcement is retained. One of the negative and dreaded effects of such an announcement is the negative psychological impact. Some studies show that the diagnostic announcement would worsen the level of anxiety or depressed mood and the risk of social isolation. On the other hand, other studies show that symptoms such as anxiety, psychic distress and depression remain stable, or even decrease slightly after the announcement of the diagnosis, in patients and their relatives. However, the literature is questionable because the majority of the studies are retrospective, mono-centric, and the patient numbers are low. While the first reactions of patients may be negative after the announcement, some report resignation experiences, or form of relief, because they have finally found a clinical explanation for the symptoms encountered. While doubt or diagnostic uncertainty, as well as the feeling of not knowing the truth, seem to have a more damaging psychological impact on the patient and those around him, increasing anxiety and confusion.
The primary objective is to study if the level of anxiety 2 months after the announcement of the diagnosis of Alzheimer's disease or a related disease is not superior to the level of anxiety before the announcement with patient / caregiver.
This present study aim to explore the feasibility with 14 patients.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Sophie DAUTRICOURT, Dr
- Phone Number: +33 +334 72 43 21 74
- Email: sophie.dautricourt@chu-lyon.fr
Study Contact Backup
- Name: Anthony BATHSAVANIS
- Phone Number: +33 +334 72 43 22 06
- Email: anthony.bathsavanis@chu-lyon.fr
Study Locations
-
-
-
Lyon, France, 69100
- Recruiting
- Hôpital des Charpennes (HCL)
-
Contact:
- Sophie DAUTRICOURT, Dr
- Phone Number: +33 +33472432174
- Email: sophie.dautricourt@chu-lyon.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients :
- Man or woman 55 years and over
- Patient received for the first time in Memory Consultation and not aware of his diagnosis
- Patient with a Mini-Mental State Assessment score (MMSE) ≥ 20
- Patient accompanied by a primary caregiver
- Patient able to provide consent to participate in research
Caregiver:
- The caregiver accompanies the patient and is considered as the main caregiver during the consultation
- is able to provide consent to participate in research
Exclusion Criteria:
- Patient living in a care homes
- Patient protected by law (under legal protection, guardianship or trusteeship)
- Patient with a hearing or visual impairment that does not allow to carry out assessments in Memory Consultation
- Patient opposing research
Study Plan
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Anxiety (Y-B form) of the State Trait Anxiety Inventory (STAI) scale
Time Frame: at inclusion
|
The anxiety score (Y-B form) of the State Trait Anxiety Inventory (STAI) scale, assess the level of anxiety in daily life.
The range of this score is from 20 to 80.
|
at inclusion
|
Anxiety (Y-B form) of the State Trait Anxiety Inventory (STAI) scale
Time Frame: at 2 months
|
The anxiety score (Y-B form) of the State Trait Anxiety Inventory (STAI) scale, assess the level of anxiety in daily life.
The range of this score is from 20 to 80.
|
at 2 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019-A02620-57
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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