Validation of MoCA-B and MoCA-Blind for Screening Cognitive Decline

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60+
SponsorUniversidade Federal do Rio Grande do Norte

About this trial

The objective of this observational study is to assess the efficacy of two neuropsychological tests (MoCA-B and MoCA-Blind) in detecting cognitive decline in older adults. The main questions it aims to answer are:

Can the results obtained by older adults on the MoCA-B distinguish between those with and without cognitive decline? Can the results obtained by older adults on the MoCA-Blind distinguish between those with and without cognitive decline?

Participants will be required to: 1. Complete a sociodemographic questionnaire; 2. Undergo a visual acuity test; 3. Complete the Pfeffer and IQCODE scales; and 4. Complete the MMSE, MoCA-B, and MoCA-Blind.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

* Older adults aged 60 and over;

Disqualifiers

Participants under 60 years of age

Participants with a prior neuropsychological, neurological, or psychiatric diagnosis that could negatively influence assessment results, such as schizophrenia, stroke within the last three months, intellectual disability, etc

Participants with self-reported or diagnosed hearing impairment (hearing loss or deafness) that is not corrected by hearing aids.

Trial population

Older adults (60 years or older) with and without cognitive decline and with and without visual impairment.

Trial design

Design model

Case-control

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

124 Participants
are grouped into 4 trial groups
Group A: older adults with cognitive decline and without visual impairment
Group B: older adults without cognitive decline (healthy) and without visual impairment
Group C: older adults with cognitive decline and with visual impairment
Group D: older adults without cognitive decline and with visual impairment

Trial outcomes

Primary outcomes

1

Optimal cut-off score for the MoCA-B and MoCA-Blind

The scores obtained by the participants (0 to 30) will be used to calculate the ROC curve and determine the optimal cutoff point (highest sensitivity and specificity) to distinguish between cognitive decline and healthy individuals.

Time frame
Assessed at baseline (Day 0)

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Universidade Federal do Rio Grande do Norte

Lead sponsor

Federal University of São Paulo

Collaborator

Universidade Federal de Goias

Collaborator

Universidade Estadual de Goiás

Collaborator

Universidade Federal do Rio Grande (FURG)

Collaborator

This trial is not recruiting at the moment. You can still explore other options: