ESAD: Autobiographical Specificity

Sponsor
Nantes University Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05642351
Collaborator
(none)
62
1
24
2.6

Study Details

Study Description

Brief Summary

Autobiographical memory is diminished in patients with Alzheimer's Disease and those with behavioral variant of frontotemporal dementia, and research has focused on the hampered ability of patients in retrieving specific memories. However, this study proposes a detailed methodology to provide a qualitative analysis of autobiographical specificity.

Condition or Disease Intervention/Treatment Phase
  • Other: Autobiographical reminder

Detailed Description

Patients with Alzheimer's Disease and those with behavioral variant of frontotemporal dementia will be invited to retrieve autobiographical memories. Memories will be analyzed and categorized into specific, categoric, extended, or semantic autobiographical retrieval.

Study Design

Study Type:
Observational
Anticipated Enrollment :
62 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Autobiographical Specificity in Alzheimer's Disease and Behavioral Variant Frontotemporal Dementia
Anticipated Study Start Date :
Mar 1, 2023
Anticipated Primary Completion Date :
Feb 28, 2025
Anticipated Study Completion Date :
Feb 28, 2025

Arms and Interventions

Arm Intervention/Treatment
Alzheimer's Disease

recruited according to criteria by National Institute on Aging (McKhann et al., 2011).

Other: Autobiographical reminder
The analysis of the specificity of Autobiographical Recall will be done through the following scale, developed for the study: 6 points for a recall involving a single personal event located in space AND time (e.g.,"I remember when my parents took me to the sea for the first time..in 1962..in Dunkerque") 5 points for a recall involving a single personal event located in space OR time ("I remember when my parents first took me to the sea...in 1962") 4 points for a recall involving a single personal event but without spatial/temporal details ("I remember when my parents took me to the sea for the first time") 3 points for a recall involving a general personal event but located in space AND time ("we used to go to Dunkerque in the summer") 2 points for a recall involving a general personal event but located in space OR time ("we used to go to Dunkerque") 1 point for a recall involving a general personal event without spatial/temporal details ("we used to go on vacation")

Behavioral variant of frontotemporal dementia

recruited following criteria by Rascovsky et al. (2011)

Other: Autobiographical reminder
The analysis of the specificity of Autobiographical Recall will be done through the following scale, developed for the study: 6 points for a recall involving a single personal event located in space AND time (e.g.,"I remember when my parents took me to the sea for the first time..in 1962..in Dunkerque") 5 points for a recall involving a single personal event located in space OR time ("I remember when my parents first took me to the sea...in 1962") 4 points for a recall involving a single personal event but without spatial/temporal details ("I remember when my parents took me to the sea for the first time") 3 points for a recall involving a general personal event but located in space AND time ("we used to go to Dunkerque in the summer") 2 points for a recall involving a general personal event but located in space OR time ("we used to go to Dunkerque") 1 point for a recall involving a general personal event without spatial/temporal details ("we used to go on vacation")

Outcome Measures

Primary Outcome Measures

  1. Autobiographical specificity [40 minutes]

    We will apply the method by Raes et al. (2007) to assess whether each retrieved event refers to a: specific event, categorical event, extended event, or semantic event

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Alzheimer' disease or avioral variant of frontotemporal dementia

  • No opposition from the patient to be included in the study

  • For Alzheimer's patients: a score of more than 24 out of 30 on the Mini Mental State Examination (McKhann et al., 1984)

Exclusion Criteria:
  • Other psychiatric/neurological disorders

  • Minor patients

  • Adults under guardianship or protection.

Contacts and Locations

Locations

Site City State Country Postal Code
1 EL HAJ Mohamad Nantes France

Sponsors and Collaborators

  • Nantes University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nantes University Hospital
ClinicalTrials.gov Identifier:
NCT05642351
Other Study ID Numbers:
  • RC22_0626
First Posted:
Dec 8, 2022
Last Update Posted:
Dec 12, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Nantes University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 12, 2022