What Elements of the Design of a Healing Garden Are Used as Landmarks by Patients With Alzheimer's Disease to Locate?

NCT ID: NCT01692977

Last Updated: 2015-07-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 77 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-08-31
• Study Completion Date: 2014-10-31

Brief Summary

The disruption of spatial orientation is considered the second most common cognitive symptom of dementia, affecting nearly all activities of daily living. Research in the field of environmental psychology has helped to highlight the influence of the environment on patients with Alzheimer's disease or related syndromes. With regard to spatial orientation, it has been shown that an environment can provide support for cognitive failures in subjects if that particular space is adapted. While numerous studies have focused on the architectural environment (hospital, housing facility), none have explored the ability of patients to orient themselves in a natural environment such as a garden. Yet, in recent years, such gardens, known as healing gardens, have emerged in housing and care facilities, providing genuine support for the care management of patients with Alzheimer-type dementia. Various works have been published outlining recommendations for their management. However, with regard to spatial orientation, none of the available research has explored the basic principles on which to rely on in order to organize the elements of outdoor spaces into itineraries that promote orientation, according to ZEISEL and TYSON (1999). In the absence of such data, these authors recommend relying on five elements, identified by Lynch in his landmark book "Image of the City" (1960), that people use to orient themselves and find their way. These are " paths ", " edges ", " districts ", " nodes " and " landmarks ". The hypothesis to verify is that patients with Alzheimer's disease do not rely on the same elements of the garden as non-Alzheimer's subjects in making orientation decisions and to mentally picture this environment.

Conditions

Alzheimer Disease

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Alzheimer disease patients

Alzheimer disease patients

Group Type: EXPERIMENTAL

neuropsychological assessment

Intervention Type: OTHER

control

healthy control subjects.

Group Type: ACTIVE_COMPARATOR

neuropsychological assessment

Intervention Type: OTHER

Interventions

neuropsychological assessment

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

All subjects (groups A and B):

• able to walk autonomously, that is without help, whether human or technical, except for a walking cane
• are aged 65 to 90 years
• have never been in the "art, memory and life" garden at the Paul SPILLMANN Centre prior to the study
• have given their written consent after receiving clear and intelligible oral and written information.

Group A : patients with Alzheimer's disease:

• diagnosis of probable Alzheimer's disease according to NINCDS-ADRDA diagnostic criteria (Mc KHANN et al., 1984)
• score less than or equal to 4 on the Hachinski ischemic scale (Hachinski et al., 1984)
• Folstein MMSE score between 10 and 24 inclusively
• score equal to 5 or 6 on the Reisberg Global Deterioration Scale (REISBERG et al., 1982).
• stable, specific treatment of Alzheimer's disease (cholinesterase and memantine)
• taking of psychotropic drugs authorized, but no change in treatment during at least the last 48 hours

Group B: healthy control subjects:

• absence of dementia according to NINCDS-ADRDA criteria (Mc KHANN et al., 1984)
• normal performance on Folstein MMSE, according to the GRECO (en français : Groupe de REflexions sur les Evaluations Cognitives) standards (Reflection Group on Cognitive Assessments)

Exclusion Criteria

For all subjects (groups A and B):

• Absence of social security coverage
• sensory deficit interfering with the task
• aphasia interfering with the task
• history of head trauma (with loss of consciousness)
• chronic alcoholism
• refusal or inability to obtain written informed consent form from the patient
• legally protected person
• severe depression: score higher than 20 on the 30-item Geriatric Depression Scale (GDS)

Group A : patients with Alzheimer's disease:

• other neurological or psychiatric diseases that may affect the assessment Group B: healthy control subjects
• neurological or psychiatric diseases that may affect the assessment

• Minimum Eligible Age: 65 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Central Hospital, Nancy, France

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thérèse Rivasseau Jonveaux, PhD

Role: PRINCIPAL_INVESTIGATOR

University Hospital of Nancy, France

Locations

University Hospital of Nancy , Saint Julien Hospital, France

Nancy, , France

Countries

France

Other Identifiers

2011-A00993-38

Identifier Type: -

Identifier Source: org_study_id