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Identification of severity-sensitive items for the detection of cognitive impairments relevant to everyday life and validation of a new procedure for the initial assessment of cognition in geriatrics - AssCo 1

Identification of severity-sensitive items for the detection of cognitive impairments relevant to everyday life and validation of a new procedure for the initial assessment of cognition in geriatrics - AssCo 1 - AssCo 1

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00036423
Enrollment
460
Registered
2025-03-26
Start date
2025-05-07
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

cognitive impairments in old age

Interventions

Group 1: Patients in geriatrics and geriatric traumatology will be examined at two points in time: - within the first two days, depending on their capacity to consent, using a delirium scale, the new
and - after stabilization, at the earliest one week after the initial assessment, via the new procedure, MMSE, Schulmann's clock test, and the Extended Barthel Index (EBI). In the period between the

Sponsors

Medizinische Hochschule Brandenburg - Theodor Fontane
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Inpatients and day patients of a geriatric clinic and a center for geriatric traumatology - Good understanding of the German language - Adequate hearing - Adequate language skills - Adequate visual acuity (MMSE and clock test) - Adequate motor skills (MMSE and clock test) - Ability to provide information and consent, or consent of the legal representative

Exclusion criteria

Exclusion criteria: - Inadequate ability to cooperate or be examined due to delirium - Inadequate ability to be examined due to very poor general condition, severe pain, or other symptoms (severe exhaustion, extreme fatigue, etc.) - Known intellectual disability - Acute danger to self or others

Design outcomes

Primary

MeasureTime frame
Correspondence of the results of the new AssCo 1 procedure with the results of the MMSE collected after stabilization of the patients during the hospital stay and with a synoptic expert opinion

Secondary

MeasureTime frame
ability of individual items to predict therapy-relevant severity of cognitive impairment

Countries

Germany

Contacts

Public ContactJan Stöcker

Medizinische Hochschule Brandenburg - Theodor Fontane

Jan.Stoecker@mhb-fontane.de+49 17623827321

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 14, 2026