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Comparison of different intervention programs to improve sensorimotor and cognitive performance of multi-morbid elderly patients

Comparison of different intervention programs to improve sensorimotor and cognitive performance of multi-morbid elderly patients - KLaR

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00005293
Enrollment
90
Registered
2013-09-11
Start date
2013-09-16
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Multimorbidity

Interventions

Group 1: Target group: 30 multi-morbid (two or more chronic diseases) elderly subjects (60-90 years) living in nursing care facilities will participate in a Yoga-based intervention program (KLaR) for

Sponsors

Deutsches Rotes Kreuz, Berlin Generalsekretariat? Team 42-Altenhilfe und Gesundheitsförderung?
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Ability to decide independently about study participation. Multi-morbidity (i.e. the presence of 2 or more chronic diseases). Clinically stable situation. Permanent residence in a nursing facility for at least 3 years. Age 60-90 years. Ability to carry out at least 2/3 of the used testing procedures Minimum of standing and walking ability (even with crutches).

Exclusion criteria

Exclusion criteria: Palliative care situation. Severe loss of vision or hearing that can not be compensated. Bad understanding of German language. Aphasia, which prevents an informed consent. Permanent confinement to bed.

Design outcomes

Primary

MeasureTime frame
Behavioural tests (A: one day before start of the intervention / B: One day after end of the intervention) to assess: Constitution (Grip-strenght with hand dynamometer, walking performance in timed up&go test, stabilometry using STABLE) Cognition (MMSE Dementia screening, Concentration test AKT) and Sensorimotor performance (proprioception testing using a goniometer, reaction times using a custom-made setup, Somnowatch based actigraphy).

Secondary

MeasureTime frame
Interviews and questionnaires (A: one day before start of the intervention / B: One day after end of the intervention) with the subjects to assess: individual well-being (VAS-based pain rating, life-contentment questionnaire FLZ, health situation using the SF8). Interviews and questionnaires with the nurses to rate the subject's constitution (Barthel index, Beltztest scales to rate everyday-life performance).

Countries

Germany

Contacts

Public ContactJan-Christoph Kattenstroth

Neural Plasticity Lab, Institut für Neuroinformatik der Ruhr-Universität Bochum

Jan-Christoph.Kattenstroth@rub.de+49 (0) 234 3224931

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026