Skip to content

Imagery in Early Stages of Dementia

The Effectiveness of Mental Imagery in Motor and Cognitive Rehabilitation in Subjects of Early Stage of Dementia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05232526
Enrollment
105
Registered
2022-02-10
Start date
2021-10-10
Completion date
2024-10-10
Last updated
2022-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dementia of Alzheimer Type, Mental Imagery

Keywords

Imagery, Exercise, Dementia

Brief summary

The purpose of the present study is to investigate the effectiveness of mental imagery (MI) in subjects with early stage of dementia. The hypothesis of the study is that MI will have a beneficial effect in motor, cognitive and emotional state in this clinical population.

Detailed description

Dementia is a disorder that is characterized by a decline in cognition involving one or more cognitive domains (learning and memory, language, executive function, complex attention, perceptual-motor, social cognition). The most common form of dementia in older adults is Alzheimer disease (AD), accounting for 60 to 80 percent of cases. Mental imagery (MI) is a technique which involves envisioning motor actions without actual execution. MI is considered an effective rehabilitative tool in athletes, Parkinson's disease, and post stroke because it engages the same or similar neural systems as the actual execution of motor actions to improve gait, gait-related, and cognitive functions having as a result improvements in gait speed, stride length, tandem stance, timed up and go, clock drawing and stroop interference. The recruitment of the population will be carried out by Day Care Centers in Athens Alzheimer Association. A group of elderly patients with early stage of dementia, aged 65 to 95 years, will participate. Information sheet and consent form will be provided to all participants. A randomized intervention study is designed to assess the efficacy of MI as therapeutic strategy for subjects with early stage of dementia and the sample will be randomized to one of the three following study groups: 1. MI and exercise program (intervention group) 2. Only exercise program (control group) 3. Neither MI nor exercise program (2nd control group). Assessment will be obtained in three-time periods: prior to the program, middle of the program and after the program.

Interventions

OTHERMental imagery (MI) and exercise program

Mental imagery and exercise program will be used to improve balance, functional status, cognitive ability, depression and quality of life of the sample

DEVICEMental Imagery and Exercise program

Questionnaires and functional tests are going to be used to evaluate balance, functional status, cognitive ability, depression and quality of life of the sample.

Sponsors

Alzheimer's Association
CollaboratorOTHER
University of West Attica
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
65 Years to 95 Years
Healthy volunteers
Yes

Inclusion criteria

* 95 years\<age\>65 years * Diagnosed early stage of dementia * Good oral and written speech and to perform orders * Both sexes * Ambulatory * No other health issues in the last month

Exclusion criteria

* Late stage of dementia * Psychiatric problems * Serious health problems * Not able to walk

Design outcomes

Primary

MeasureTime frameDescription
Change is being assessed (Change from Baseline Balance at 12 weeks)Prior to the 1st week of the program, the 12th week of the programThe Berg Balance Scale (BBS) is used to objectively determine a subject's ability to safely balance during a series of predetermined tasks. It is a 14 item list with each item consisting of a 5-point ordinal scale ranging from 0 to 4, with 0 indicating the lowest level of function and 4 the highest level of function and takes approximately 20 minutes to complete.
Change is being assessed (Change from Baseline Stability at 12 weeks)Prior to the 1st week of the program, the 12th week of the programThe Multidirectional Reach Test (Reach in Four Directions Test) is a screening tool to determine the limits of stability of subjects in 4 directions: forward, backward, leftward and rightward. Subjects performed maximal outstretched arm reach in each direction with their feet flat on the floor.
Change is being assessed (Change from Baseline Siti-to-stand ability at 12weeks)Prior to the 1st week of the program, the 12th week of the programThe Five Times Sit-to-Stand Test (FTSST) is considered to be a useful, consistent and low-cost tool to assess sit-to-stand ability. The FTSST measures the time taken to stand five times from a sitting position as quickly as possible that measures of lower limb strength, balance control and exercise capacity.
Change is being assessed (Change from Baseline Functional status at 12 weeks)Prior to the 1st week of the program, the 12th week of the programThe Timed Up and Go test (TUG) is a simple test used to assess a person's mobility. It measures the time that a subject takes to rise from a chair, walk three meters, turn around 180 degrees, walk back to the chair, and sit down while turning 180 degrees.

Secondary

MeasureTime frameDescription
DepressionPrior to the 1st week of the program, the 6th week of the program, the 12th week of the programThe Short-Form of Geriatric Depression Scale (SF-GDS) is a 15-question screening tool for depression in older adults, using a Yes/No format. It takes 5-7 minutes to complete and is filled out by the researcher with minimal training in its use.
Quality of lifePrior to the 6th week of the program, the 6th week of the program, the 12th week of the programThe Euro-Qol 5 Dimensions 5 Level of severity scale (Euro-Qol 5D-5L scale) is a preference-based Health Related Quality of Life measure which includes 5 domains, i.e., mobility, self-care, usual activities, pain/discomfort, anxiety/depression. The core of all domains ranges from 1 (best score) up to 5 (worse score). The total perceived quality of life will be graded by the patient. Also it includes a Visual Analog Scale (VAS), by which respondents can report their perceived health status with a grade ranging from 0 (the worst possible health status) to 100 (the best possible health status).
Cognitive abilityPrior to the 1st week of the program, the 6th week of the program, the 12th week of the programThe Walking While Talking Test (WWITT) is a dual-task measure to examine cognitive-motor interactions. During the WWTT, subjects walk at self-paced speed for 6 meters before turning and walking back to the starting point. During the walking subjects recite 12 Greek alphabet letters (each letter at each step) starting with A (ΑΒΓΔ, ΚΛΜΝ, ΠΡΣΤ) until the starting point. Time and errors in the alphabet will be recorded.

Countries

Greece

Contacts

Primary ContactAnna Christakou, PhD
achristakou@uniwa.gr+306977370284
Backup ContactVasiliki Sakellari, Pr
vsakellari@uniwa.gr+306979033952

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 9, 2026