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Clinical Trials/NCT06044818
NCT06044818RecruitingNot Applicable

Validación Del Sistema de Cribaje y Seguimiento de acceXible Para depresión.

Accexible1 site in 1 country178 target enrollmentStarted: January 22, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
178
Locations
1
Primary Endpoint
Prevalence of Depression

Study Overview

Brief Summary

Major depressive disorder (MDD) is a chronic disease with a prevalence around 8-12% and is considered one of the most debilitating disease worldwide.

A recent orientation is the analysis of language in relation to the description of images with a high and varied semantic and emotional content. It can be studied that changes in the description of an image check if these changes are associated with the evolution of a person with probable impairment both in memory and cognitive as well as emotional, psychiatric, behavioral and even in their interaction with environmental factors especially those associated with socialization and loneliness.

The present study has the objective of validating Accexible as a tool for Screening and Monitoring Depression.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adult 18-65 years of age.
  • Participants must have Spanish as their first language (able to speak and understand verbal messages).
  • Participants must have mobile phone with internet.
  • Participants must have the ability to understand AcceXible's basic instructions.
  • Participants must agree to participate in the study and have voluntarily signed the informed consent.
  • Exclusion Criteria for patients:
  • To have received a diagnosis of neurodegeneration.
  • To have significant vision problems that would affect the ability to perceive visual stimuli.
  • To have significant hearing problems that would affect the ability to understand verbal cues.
  • To be unable to give informed consent to participate in the study.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Prevalence of Depression

Time Frame: An average of 1 year

questionnaire

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Accexible
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (1)

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