Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Functional Skills Training for Supermarket Shopping Using NFC Technology in People With Intellectual Disabilities

16 de junio de 2026 actualizado por: Javier Pereira, Universidade da Coruña

The general objective of the "Compra con-Migo" project is to evaluate the impact of a technological tool based on NFC (Near Field Communication) technology on the development of cognitive and instrumental skills necessary to carry out the activity of shopping in supermarkets in people with intellectual disabilities. Specifically, it is intended to analyze the evolution of performance in tasks such as planning, product recognition, calculation, payment and functional autonomy, after the use of an adapted gamified application.

The research is structured as a pilot, analytical, longitudinal and prospective study, without a control group, with evaluations in three moments: pre-intervention, intermediate and post-intervention. This methodological decision responds both to ethical criteria, by avoiding denying a potentially beneficial intervention, and to logistical limitations typical of institutional environments. Statistical analysis will be performed with R, using analysis tools for repeated measurements, both parametric and non-parametric, as appropriate.

The study population is composed of adults with intellectual disabilities, aged between 18 and 65 years, who regularly take part in therapy sessions in specialized centers. A sample of between 34 and 40 participants is expected. The intervention will be carried out in various Care Centers for People with Disabilities (CAPD) and associations in Galicia (Spain), specifically in the CAPD of A Coruña, Chapela, Sarria, Souto de Leixa and the O Saiar Occupational Center.

This study will not only evaluate the use of the tool in real environments, but also generate evidence applicable to its future implementation in other contexts. The proposal is aligned with the principles of accessibility, technological innovation and social inclusion, and seeks to offer a structured, motivating and effective therapeutic resource.

Descripción general del estudio

Estado

Terminado

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

20

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • A Coruña
      • A Coruña, A Coruña, España, 15008
        • Centro de Investigación en TIC (CITIC)

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

No

Descripción

Inclusion Criteria:

  • People with disabilities who regularly participate in therapy sessions.
  • People with disabilities within the age range between 18 and 65 years.
  • Participants who agree and have signed the informed consent to participate in the study and the authorization for data collection.

Exclusion Criteria:

  • Individuals with disabilities that limit the ability to interact with the tool (e.g., severe visual, hearing, or cognitive difficulties) that significantly limit the ability to interact with the tool.
  • Participants who are unable to regularly attend scheduled therapy sessions, affecting consistency in the intervention.
  • Participants with unstable medical or psychological conditions who may experience aggravation of their condition due to interaction with the tool.
  • Participants who are involved in other interventions or studies that may influence the results of this protocol.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: General group

The intervention will take place over eight weeks, with a frequency of two weekly sessions in which participants will work with the "Compra con-Migo" (Shop with Me) application. Each session will be supervised by the center's professional, ensuring that the participant can interact with the application autonomously to the best of their ability. The following elements will be required for the development of each session:

  • Intervention record document.
  • Tablet with the "Compra con-Migo" app installed.
  • Baskets.
  • Physical objects in representation of purchase products. The user will carry out the intervention, which will consist of completing five shopping lists pre-designed by the research team. Each list will involve scanning 5 objects and simulating a payment.

After completing four weeks of intervention, an intermediate evaluation will be carried out to analyze the progress made so far. In addition, a proprietary evaluation tool will be applied.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Level of Performance Shown by the Participant During the Performance of the Purchase Simulation
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks

The Basic Everyday Living Skills (BELS) scale will be administered. Standardized and validated tool in the Spanish context designed to assess changes in the performance of daily living skills. It is made up of 26 questions, each of which describes a specific behavior. Each question is divided into two scales:

  • A three-part scale on the degree of opportunity to carry out activities independently.
  • A five-part scale on the actual level of completion of each activity of daily living.
From enrollment to the end of treatment at 8 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Quality of Performance Shown by the Participant while Using the "Compra con-Migo" tool
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks
A structured observation log designed by the investigators will be administered, attached by ad hoc observation record.
From enrollment to the end of treatment at 8 weeks
Score in Dependency during Purchase Activity
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks

The Lawton and Brody Scale will be used for the Instrumental Activities of Daily Living. A standardized and validated tool in the Spanish context designed to assess the degree of functional autonomy of a person in the performance of instrumental tasks necessary to live independently in the community.

This scale allows you to identify limitations in activities that are more complex than the basic ones, such as: using the telephone, preparing meals or making purchases. Each item is scored based on the level of independence or dependence with which the person performs the task, giving rise to a total score that allows the level of autonomy of the person being evaluated to be categorized, from 0 (total dependence) to 8 (independence).

From enrollment to the end of treatment at 8 weeks
Total Number of Errors made by the Participant when Selecting or Scanning the Wrong Products
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks
Automatic registration by the application.
From enrollment to the end of treatment at 8 weeks
Errors at the Calculation and Payment Stage
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks
Number of errors when making the payment (incorrect use of coins/notes, wrong scanning). Automatic registration by the application.
From enrollment to the end of treatment at 8 weeks
Time of Completion of the Activity
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks
Total time (in seconds) from the start to the end of the shopping list.
From enrollment to the end of treatment at 8 weeks
Level of Satisfaction, Usability and Quality of the "Compra con-Migo" Tool by Professionals.
Periodo de tiempo: From enrollment to the end of treatment at 8 weeks
A structured record designed by the researchers.
From enrollment to the end of treatment at 8 weeks

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Director de estudio: María Martínez Pérez, Computer Science, Universidade da Coruña
  • Director de estudio: Betania Groba Gonzalez, Ocupational Therapy, Universidade da Coruña
  • Director de estudio: Patricia Concheiro Moscoso, Ocupational Therapy, Universidade da Coruña

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

2 de junio de 2025

Finalización primaria (Actual)

21 de noviembre de 2025

Finalización del estudio (Actual)

23 de noviembre de 2025

Fechas de registro del estudio

Enviado por primera vez

8 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

16 de junio de 2026

Publicado por primera vez (Actual)

22 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

22 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

16 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Suscribir