Emotional State Measurement Trial (EMOPROEXE): A Protocol for Promoting Exercise in Adults and Children with Cerebral Palsy

Author:

Gómez-González Isabel M.12ORCID,Castro-García Juan A.12ORCID,Merino-Monge Manuel1ORCID,Sánchez-Antón Gemma1ORCID,Hamidi Foad3ORCID,Mendoza-Sagrera Alejandro4,Molina-Cantero Alberto J.1ORCID

Affiliation:

1. Departamento de Tecnología Electrónica, E.T.S.I. Informática, Universidad de Sevilla, 41012 Sevilla, Spain

2. Instituto Universitario de Investigación de Ingeniería Informática, Universidad de Sevilla, 41012 Sevilla, Spain

3. Information Systems Department, University of Maryland, College Park, MD 20742, USA

4. Asociación Sevillana de Parálisis Cerebral, 41704 Dos Hermanas, Spain

Abstract

Background: The protocol described in this paper is part of a research project coordinated between three Spanish universities, where a technology aimed at improving the quality of life of people with cerebral palsy will be developed. Part of the proposed technology will consist of an interface and a series of applications to increase motivation for daily physical activity. The basis of these developments is the measurement of the emotional state of the subjects. Methods: The experimental protocol is designed with two research objectives, on the one hand to identify the emotional state through physiological signals, and on the other to determine whether music can be a motivating factor to promote physical activity. It is specifically designed for subjects with cerebral palsy, taking into account the special characteristics of this population. These are people with whom it is difficult to use questionnaires to have a basis to contrast with the measured physiological signals, so measurements must be taken in carefully chosen daily-life situations. Discussion: We hope our findings show which physiological parameters are the most robust to measure the emotional state and how to design rehabilitation and physical activity promotion routines that are motivating, in addition to being able to avoid risk factors during the performance of these routines. Trial registration: NCT05621057.

Funder

FIDETIA

Publisher

MDPI AG

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