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OpenTrials
Completed

NCT Number: NCT05202197

Smart Cupboard-based System for Memory Assessment in Alzheimer's Patients

The main objective of the research is to create a tool that can make a good diagnosis of cognitive abilities in Alzheimer's patients. As a secondary objective, the investigators intend to examine both the percentage of correct answers and the response times and see their relationship with age, gender, sex, months since the onset of the disease and years of training.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Zaragoza

Teruel, 44003, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being over 18 years.
  • Provide signed informed consent.
  • Have the ability to understand the study.

Exclusion criteria

Having any physical or medical problem that prevents or advises them not to stand upright, in a bipedal position.

Treatment and study plan

Smart cupboard

Other

Development of a memory task with the help of a smart cupboard

Primary outcomes

  1. Accuracy response.

    Time frame: 60 minutes

    Number of successes / failures on the total of questions

  2. Reaction time

    Time frame: 60 minutes

    Defined as the time it takes the subject to answer each of the questions.

Sponsors and collaborators

Lead sponsor

Universidad de Zaragoza

Other

Registry information

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jan 21, 2022
Registry last updated
Feb 7, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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