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Spanish Adaptation and Validation of the Everyday Cognition Battery (ECB).

NCT04169633 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2019-11-20

No results posted yet for this study

Summary

HYPOTHESIS:

The Spanish version of the Everyday Cognition Battery Scale (ECB) is valid and reliable in the Spanish population.

OBJECTIVES:

• Providing a validated scale in Spanish to evaluate daily cognition in older adults.

SPECIFIC OBJECTIVES:

* Translating the original English version of the ECB into Spanish.
* Adapting the scale to the sociocultural context of Spain.
* Checking the psychometric characteristics (reliability and validity) of the translated version .

STUDY DESIGN:

Cross-sectional descriptive study. Permission to use the ECB scale will be requested to the author, Allaire JC. Translation and adaptation of the scale.

Administration of the four tests of the ECB to the individuals participating in the study.

Administration of the Rapid Evaluation of Cognitive Functions (RECF) and Lawton and Brody scales.

Analysis of the psychometric characteristics of the translated version.

The protocol has been authorized by the Ethics Committee of the Salamanca health area to make the project possible.

Conditions

  • Occupational Therapy
  • Nursing Caries
  • Aging Disorder
  • Cognitive Disorders

Interventions

DIAGNOSTIC_TEST

Cognitive Function Evaluation

Evaluation of cognitive function and evaluation of daily cognition

Sponsors & Collaborators

  • University of Salamanca

    lead OTHER

Principal Investigators

  • Eduardo José IP Fernández, PhD · University of Salamanca

Eligibility

Min Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2018-04-01
Primary Completion
2020-12-31
Completion
2020-12-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04169633 on ClinicalTrials.gov