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Physiotherapist Overseen Whole-body Exercises for Residents with Dementia: a non-randomized pilot study

Physiotherapist Overseen Whole-body Exercises for Residents with Dementia: a non-randomized pilot study - (POWER-D)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON57434
Enrollment
36
Registered
2025-03-05
Start date
2025-03-05
Completion date
Unknown
Last updated
2026-05-18

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

Conditions

Therapietrouw, mogelijke nadelige effecten, ervaringen, spierkracht, evenwicht, loopsnelheid, mobiliteit, zelfstandigheid in dagelijkse zorgtaken, psychiatrische gedragsproblemen bij dementie Adherence experiences

Interventions

two times per week 45 minutes group exercise with strength and balance exercises, two times per week 20 minutes aerobic stationary cycling on self-selected resistance

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - By a physician documented diagnosis of dementia in the patient file. In the Nether-lands, the diagnosis of dementia is usually made before admission to the nursing home. The primary physician or a geriatric specialist can make the diagnosis, and there is no legislation according to what criteria the diagnosis can be made. - Able to walk 50 meters without the help of a person (walking aids are allowed). - Informed consent by the family/informal caregiver in charge. - No expected resistance to the intervention, as perceived by the physician in charge.

Exclusion criteria

Exclusion criteria: - Behavioural problems that interfere with participation in a group intervention, according to the physician in charge and/or the psychologist in charge. - Other factors listed by the physician in charge that could make it unfavourable for the resident to take part in the study

Design outcomes

Primary

MeasureTime frame
Primary study parameters that will be evaluated at the end of the intervention (13 weeks): Adherence to the intervention regarding successfully followed exercise sessions in relation to total available sessions; adverse events related to the intervention; the experiences of participants and exercise conductors.

Secondary

MeasureTime frame
Secondary study parameters: the effects on physical performance (strength, static balance, walking speed, mobility) assessed with the Short Physical Performance Battery and the Timed Up and Go, ADL independence with the Functional Independence Measure, and neuropsychiatric symptoms of dementia assesses with the Neuropsychiatric Inventory-Nursing Hom

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: May 22, 2026