Exergaming in People With Major Neurocognitive Disorder

Davy Vancampfort

Status: Unknown

Conditions: Major Neurocognitive Disorder; Randomised Controlled Trial; Physical Activity; Long-term Care Facility; Cognitive Impairment

Treatments: Device: Exergame device

Study type: Interventional

Funder types: Other

Identifiers

NCT04436302

042020

Details and patient eligibility

About

This randomized controlled trial explores the efficacy of an 8-week standing exergaming program in people with major neurocognitive disorder (MNCD) residing in long-term care facilities.

Full description

This randomized controlled trial explores the efficacy of an 8-week standing exergaming program in people with major neurocognitive disorder (MNCD) residing in long-term care facilities. Fifty inpatients with mild to moderate MNCD will be randomly assigned to three times weekly for eight weeks 15 min of exergaming versus watching preferred music videos. The Montréal Cognitive Assessment (MoCA), Short Physical Performance Battery (SPPB), Neuropsychiatric Inventory (NPI), Cornell Scale for Depression in Dementia (CSDD), Dementia Quality of Life (DQoL), Katz activities of daily living (ADL) and Instrumental ADL (IADL) are measured at baseline and post intervention.

Enrollment: 50 estimated patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion criteria included:

• a Diagnostic and Statistical Manual of Mental Disorders (DSM) 5 diagnosis of MNCD (American Psychiatric Association, 2013)
• aged 65 years or older
• a score of minimum 10 on the Mini-Mental State Examination (MMSE)
• residing at least two weeks in the care facility at the time of inclusion
• being physically capable of doing standing exercises (whether or not with extra support).

Possible causes of MNCD were vascular dementia, Alzheimer's disease, mixed dementia, Parkinson's disease or Lewy body disease.

Exclusion criteria consisted of:

• any unstable cardiovascular or other health condition which according to the American College of Sports Medicine Standards might lead to unsafe participation
• a score lower than 10 on the MMSE
• a planned transfer to another setting within the following two months.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Sequential Assignment

Masking: Single Blind

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50 participants in 2 patient groups

Intervention

Experimental group

Description:

Dividat senso exergame device

Treatment:

Device: Exergame device

Control

Active Comparator group

Description:

Listening to music

Treatment:

Device: Exergame device