MoCA-Norm: Normative Values for the German Version of the Montreal Cognitive Assessment (MoCA)

Sponsor
Andreas Monsch (Other)
Overall Status
Completed
CT.gov ID
NCT03246269
Collaborator
(none)
334
4

Study Details

Study Description

Brief Summary

This observational cohort study in healthy volunteers establishes normative data for the German version of the Montreal Cognitive Assessment (MoCA) and investigates the possible impacts of demographics on the MoCA total score.

Detailed Description

The Montreal Cognitive Assessment (MoCA) is a short tool to evaluate a multitude of cognitive domains (visuospatial / executive functioning, object naming, memory, attention, language, abstraction, orientation). The original English MoCA consistently showed very high sensitivity and specificity in distinguishing patients with mild cognitive impairment from healthy controls. Therefore it is an excellent tool for early recognition of cognitive disorders. Based on a Canadian sample, the MoCA proposes a cut-off-value of 26/30 points. However, there is increasing evidence of intercultural differences in terms of the best cut-off-score. In addition the original version only slightly corrects for possible influences of education - an adjustment for age- or gender-related effects is missing. Therefore, the aim of our study was to investigate the possible impacts of demographics on the MoCA total score and to provide normative values for a German-speaking population.

Study Design

Study Type:
Observational
Actual Enrollment :
334 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Normative Values for the German Version of the Montreal Cognitive Assessment (MoCA)
Actual Study Start Date :
Dec 1, 2016
Actual Primary Completion Date :
Apr 1, 2017
Actual Study Completion Date :
Apr 1, 2017

Arms and Interventions

Arm Intervention/Treatment
MoCA cohort

The German MoCA is administered once to all study participants.

Diagnostic Test: MoCA

Outcome Measures

Primary Outcome Measures

  1. Montreal Cognitive Assessment (MoCA) - German version [Baseline]

    Total score of the MoCA

Secondary Outcome Measures

  1. Mini-Mental State Examination (MMSE) [Baseline]

    Total score of the MMSE

  2. Geriatric Depression Scale (GDS) [Baseline]

    Total score of the GDS

  3. Consortium to Establish a Registry for Alzheimer's Disease - Neuropsychological Assessment Battery (CERAD-NAB) [Baseline]

    Total score of the CERAD-NAB

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Age ≥65 years

  • Education ≥7 years

  • Fluency in the German language

  • Written informed consent

Exclusion Criteria:
  • History of cognitive impairment

  • Depression

  • Severe sensory or motor impairment interfering with cognitive testing

  • Serious somatic disease

  • Disease or event affecting the central nervous system

  • Cerebrovascular disease

  • Regular medication with psychoactive drugs except for benzodiazepines

  • Participation in a cognitive study within the last 3 months

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Andreas Monsch

Investigators

  • Principal Investigator: Alessandra Thomann, MSc, Felix Platter Hospital Basel
  • Principal Investigator: Nicolai Goettel, MD, University Hospital, Basel, Switzerland
  • Principal Investigator: Raphael Monsch, MD, University Hospital, Basel, Switzerland
  • Principal Investigator: Manfred Berres, PhD, University of Applied Sciences Koblenz
  • Study Chair: Andreas Monsch, PhD, Felix Platter Hospital Basel

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Andreas Monsch, PhD, University Hospital, Basel, Switzerland
ClinicalTrials.gov Identifier:
NCT03246269
Other Study ID Numbers:
  • MoCA-Norm
First Posted:
Aug 11, 2017
Last Update Posted:
May 31, 2018
Last Verified:
May 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 31, 2018