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Introduction: The use of video games has become widespread worldwide. Excessive use of video games is increasingly becoming a matter of concern, particularly in patients diagnosed with Attention Deficit Hyperactivity Disorder (ADHD). Currently, internet gaming disorder (IGD) is not included within the DSM-5-chapter Disorders related to substances and addictive disorders. Methods: This is a post-hoc descriptive naturalistic study comparing children and adolescents diagnosed with ADHD with and without IGD. We used the 85% cut-off point of the test ADITEC-V for video game addiction to split our sample of ADHD patients into those with IGD (>=85%) and those without IGD (<85%). Results: 13 (25%) out of the 51 children and adolescents with ADHD included in our study had an IGD. Patients with IGD had a first contact with internet, smartphones, and videogames at a very early age (5.67 ± 3.31, 6.33 ± 4.60, and 7.50 ± 2.61, respectively). However, only age at first contact with the internet was statistically significantly different when comparing ADHD patients with and without IGD (8.68 ± 2.71 vs. 5.67 ± 3.31, t = 3.166, df = 47, p = 0.01). Different neurodevelopmental, clinical, and neuropsychological measures converging in impulsivity is a risk factor for IGD. Unexpectedly, we found no association between IGD and poor academic achievement. Discussion: Future studies may include randomized controlled trials for treating IGD, the study of social adjustment as a protective factor against developing an IGD, and the role of serious and non-serious video games in the development of an IGD, among others. Additional research is clearly needed on IGD.
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BACKGROUND: Compared with traditional approaches, gaming strategies are promising interventions for the treatment of attention-deficit/hyperactivity disorder (ADHD). We developed a serious game, The Secret Trail of Moon (TSTM), for ADHD treatment. OBJECTIVE: The main objective of this clinical trial was to demonstrate the effectiveness of an add-on, either TSTM or Therapeutic Chess (TC), in previously optimally drug-titrated, clinically stable patients with ADHD. METHODS: This study is a prospective, unicentric, randomized clinical trial in clinically stable patients with ADHD, aged 12 to 22 years. The TSTM (n=35) and TC groups (n=34) performed 12 weekly sessions of their respective treatments. The control group (CG) patients (n=35) were called by phone every week, but they received no cognitive intervention. The primary end point was the change from baseline to end point in the parent "Behavior Rating Inventory of Executive Function-2" (BRIEF-2; patients' parents) in the per-protocol population (31 serious videogame: 24 TC and 34 CG). RESULTS: Our study failed to probe clear-cut improvements in the global score of the BRIEF-2. However, the TC group showed improvements in measures of emotional control, emotional regulation, and inattention. The TSTM group showed improvements in measures of emotional regulation, inattention, and school context. CONCLUSIONS: TSTM and TC did not improve executive function symptoms, but they improved ADHD symptomatology related to emotional regulation. Further studies with bigger samples are required to confirm these preliminary findings. TRIAL REGISTRATION: ClinicalTrials.gov NCT04355065; https://clinicaltrials.gov/ct2/show/NCT04355065.
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La aplicación de las nuevas tecnologías (NNTT) a la evaluación psicológica puede ampliar enormemente la capacidad de los profesionales para evaluar de forma más precisa y exhaustiva y agilizar los procesos de recogida y análisis de información. Para poder acceder a estas ventajas hay que considerar también los costes, desafíos y amenazas potenciales derivados de la implantación de estos nuevos sistemas de evaluación. Con este objetivo, en este trabajo se abordará en primer lugar en qué grado los profesionales de la psicología, los usuarios y las organizaciones están preparados para adoptar el uso de las NNTT. A continuación, se comentará el impacto que la aplicación de la tecnología está teniendo en los propios instrumentos y en el papel que los profesionales desempeñan. Tras este punto, se cuestionará en qué grado puede darse una cierta fascinación por las NNTT que ciega el análisis de los criterios psicométricos esenciales para cualquier medida. Finalmente, se apuntarán algunos desafíos que los creadores y editores de test deben afrontar durante el desarrollo de instrumentos basados en NNTT.(AU)
The application of new technologies to the field of psychological assessment can greatly enhance the ability of professionals to carry out assessments more accurately and comprehensively and to streamline the processes of collecting and analyzing information. In order to access these benefits, the costs, challenges, and potential threats associated with the implementation of new assessment systems must also be considered. To this end, this paper will first address the extent to which psychology professionals, users, and organizations are prepared to adopt the use of new technologies. Then, we will discuss the impact that the application of technology is having on the instruments themselves and on the role that professionals play during the process. After this, we will question the extent to which a certain fascination with technology can blind the analysis of the essential psychometric criteria for any measurement. Finally, we will identify some of the challenges that test developers and publishers must face during the development of instruments based on new technologies.(AU)
Subject(s)
Humans , Behavior , Personality Assessment , Psychological Tests , Technology , Information Technology , Inventions , Psychology , Psychology, Clinical , Psychology, Social , 57970ABSTRACT
Objective: Serious videogames and virtual reality (VR) have gained increasing interest for treating attention deficit hyperactivity disorder (ADHD). "The Secret Trail of Moon" (TSTM) study is a clinical trial devoted to testing the efficacy of TSTM, a VR serious videogame developed to train in five major cognitive skills usually compromised in patients with ADHD. This study is a three-arm nonequality trial comparing TSTM to online chess training and a control group (CG). This study aims to demonstrate that augmentation with either TSTM or online chess is efficacious in clinically drug-stable patients with ADHD. Materials and Methods: This study is prospective, unicentric, and randomized with a CG. One hundred five patients with ADHD, ages 12-22 years old, and pharmacologically stable were enrolled. Patients were randomized into three groups: TSTM group, online chess group (therapeutic chess [TC]), and CG. Objective and subjective measures of the patient and parents are included. Patient visits differ for each group. TSTM group patients have 15 face-to-face visits: preinclusion visit, inclusion visit, 12 training visits, and final visit. TC and CG patients have 3 face-to-face visits (preinclusion, initial visit, and final visit) and 12 e-mail or phone communications during training (TC) or follow-up (CG group). This study was approved by the local Institutional Review Board (IRB). Results: Not applicable. This is a study protocol. Conclusion: This is the first study testing an augmentation strategy using either a serious videogame or chess in clinically drug-treated patients with ADHD. Using VR serious videogames present with several advantages over traditional videogames. Trial Registration: NCT04355065.
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Attention Deficit Disorder with Hyperactivity/psychology , Video Games/standards , Virtual Reality , Adolescent , Child , Female , Games, Recreational/psychology , Humans , Male , Prospective Studies , Video Games/psychology , Young AdultABSTRACT
ANTECEDENTES: en ciencias sociales, del comportamiento y de salud es habitual usar tests breves. El tamaño del test puede afectar a la correcta identificación de ítems con DIF. Este trabajo compara la eficacia relativa de la Regresión Logística Discriminante (RLD) e IRTLRDIF en la detección del DIF en tests cortos politómicos. MÉTODO: se diseñó un estudio de simulación. Se manipuló tamaño del test, tamaño de la muestra, cantidad DIF y número de categorías de respuesta al ítem. Se evaluó el Error Tipo I y la potencia. RESULTADOS: en las condiciones de no-DIF IRTLRDIF y RLD mostraron tasas de Error Tipo I cercanas al nivel nominal. En tests con DIF las tasas de Error Tipo I dependieron del tamaño del test, de la muestra, cantidad de DIF, contaminación del test y número de categorías del ítem. RLD presentó mayor tasa de Error Tipo I que IRTLRDIF. La potencia estuvo afectada por la cantidad de DIF y tamaño de la muestra. En tests muy cortos RLD mostró mayor potencia que IRTLRDIF. CONCLUSIONES: en tests cortos y con DIF las tasas de Error Tipo I fueron elevadas. La potencia de IRTLRDIF y RLD fue relativamente baja en tests cortos y tamaños muestrales pequeños BACKGROUND: COOMPLEC.Sec is a reading comprehension test for secondary students, conceived from a multidimensional perspective in line with large-scale educational surveys such as PISA or PIRLS. The objective of this study was to validate the theoretical model of ECOMPLEC.Sec. A bifactor model that postulates the existence of a general reading comprehension factor and three specific factors provided a good fit to the data. METHOD: 1,912 adolescents (13-18 years) participated in this study. Data analysis included construct validity via confirmatory factor analysis, and factors were regressed onto observed covariates for the interpretation of the constructs. Reliability was calculated from a non-linear SEM in order to justify the interpretability of the observed scale and subscale scores. RESULTS: the bifactor model exhibited a significantly better fit to the data than the second-order model. Furthermore, construct validity analysis suggests the existence of specific reading comprehension factors. Finally, the reliability study also supports the idea of using a total score to obtain a measure of reading comprehension. CONCLUSIONS: ECOMPLEC.Sec displays a valid parsimonious factor structure, as well as metric properties that make it a suitable tool to assess reading comprehension
ANTECEDENTES: ECOMPLEC.Sec es una prueba de comprensión lectora para estudiantes de Secundaria concebido desde una perspectiva multidimensional en consonancia con las pruebas educativas de gran escala como PISA o PIRLS. El objetivo de este estudio fue la validación del modelo teórico de ECOMPLEC.Sec. Un modelo bifactorial que presupone la existencia de un factor general de comprensión lectora y tres factores específicos ajustó adecuadamente a los datos. MÉTODO: 1.912 adolescentes (edades entre 13-18 años) participaron en este estudio. Los análisis estadísticos incluyen un análisis factorial confirmatorio cuyos factores se predicen por cuatro covariables con el fin de aportar significado a los constructos. La fiabilidad se abordó desde un modelo no lineal SEM para ayudar en la interpretación de las puntuaciones observadas de las escalas y subescalas. RESULTADOS: el modelo bifactorial exhibió un ajuste significativamente mejor que el modelo factorial de segundo orden. Las evidencias de validez de constructo apuntan a la existencia de factores específicos de comprensión lectora. CONCLUSIONES: ECOMPLEC.Sec muestra una estructura factorial parsimoniosa junto con unas propiedades psicométricas que hacen de ella una prueba adecuada para evaluar la comprensión lectora
Subject(s)
Humans , Male , Female , Adolescent , Adolescent Behavior/psychology , Psychology, Adolescent/education , Psychology, Adolescent/organization & administration , Psychometrics/methods , Psychometrics/trends , Language Tests/statistics & numerical data , Language Tests/standards , Comprehension/physiology , Psychometrics/instrumentation , Psychometrics/organization & administration , Psychometrics/standards , Factor Analysis, Statistical , Mental Competency/standardsABSTRACT
BACKGROUND: ECOMPLEC.Sec is a reading comprehension test for secondary students, conceived from a multidimensional perspective in line with large-scale educational surveys such as PISA or PIRLS. The objective of this study was to validate the theoretical model of ECOMPLEC.Sec. A bifactor model that postulates the existence of a general reading comprehension factor and three specific factors provided a good fit to the data. METHOD: 1,912 adolescents (13-18 years) participated in this study. Data analysis included construct validity via confirmatory factor analysis, and factors were regressed onto observed covariates for the interpretation of the constructs. Reliability was calculated from a non-linear SEM in order to justify the interpretability of the observed scale and subscale scores. RESULTS: The bifactor model exhibited a significantly better fit to the data than the second-order model. Furthermore, construct validity analysis suggests the existence of specific reading comprehension factors. Finally, the reliability study also supports the idea of using a total score to obtain a measure of reading comprehension. CONCLUSIONS: ECOMPLEC.Sec displays a valid parsimonious factor structure, as well as metric properties that make it a suitable tool to assess reading comprehension.
Subject(s)
Comprehension , Psychometrics , Reading , Adolescent , Factor Analysis, Statistical , Humans , Models, Theoretical , Reproducibility of ResultsABSTRACT
BACKGROUND: The prevalence and predictors of functional status and disability of elderly people have been studied in several European countries including Spain. However, there has been no population-based study incorporating the International Classification of Functioning, Disability and Health (ICF) framework as the basis for assessing disability. The present study reports prevalence rates for mild, moderate, and severe/extreme disability by the domains of activities and participation of the ICF. METHODS: Nine populations surveyed in previous prevalence studies contributed probabilistic and geographically defined samples in June 2005. The study sample was composed of 503 subjects aged ≥75 years. We implemented a two-phase screening design using the MMSE and the World Health Organization-Disability Assessment Schedule 2nd edition (WHO-DAS II, 12 items) as cognitive and disability screening tools, respectively. Participants scoring within the positive range of the disability screening were administered the full WHO-DAS II (36 items; score range: 0-100) assessing the following areas: Understanding and communication, Getting along with people, Life activities, Getting around, Participation in society, and Self-care. Each disability area assessed by WHO-DAS II (36 items) was reported according to the ICF severity ranges (No problem, 0-4; Mild disability, 5-24; Moderate disability, 25-49; Severe/Extreme disability, 50-100). RESULTS: The age-adjusted disability prevalence figures were: 39.17 ± 2.18%, 15.31 ± 1.61%, and 10.14 ± 1.35% for mild, moderate, and severe/extreme disability, respectively. Severe and extreme disability prevalence in mobility and life activities was three times higher than the average, and highest among women. Sex variations were minimal, although life activities for women of 85 years and over had more severe/extreme disability as compared to men (OR = 5.15 95% CI 3.19-8.32). CONCLUSIONS: Disability is highly prevalent among the Spanish elderly. Sex- and age-specific variations of disability are associated with particular disability domains.
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Disability Evaluation , Disabled Persons/classification , International Classification of Diseases , Mass Screening/methods , Activities of Daily Living , Aged , Aged, 80 and over , Disabled Persons/statistics & numerical data , Female , Humans , Male , Prevalence , Spain/epidemiologyABSTRACT
BACKGROUND: Despite the fact that the current definitions of dementia in the DSM-IV and ICD-10 require functional deterioration for the diagnosis of dementia, it is not necessary a formal evaluation of functional capacity. OBJECTIVES: To examine the efficiency of functional assessment as a method of screening dementia in population studies. METHODS: This systematic review was based on information from MEDLINE, EMBASE, Index Médico Español (IME), and related articles. The studies included are population studies of patients over 65, in which normal and demented (established diagnosis) subjects are compared. In all of them, subjects were evaluated using the instrumental activities of daily living scale (IADL) as the method of screening for dementia. RESULTS: Two thousand three hundred and three abstracts and bibliographical references were reviewed. The authors of the selected studies were contacted and asked about other ongoing studies or indexes not included in our review in order to complete a meta-analysis. Finally, five studies were selected (n = 11.960). A meta-analysis was performed, with a statistical Q* value of 0.88 (SE 0.26). CONCLUSIONS: The functional assessment of the IADL showed an acceptable efficiency for the screening of dementia in the population studies included in this review, although few studies have verified this efficiency (sensitivity and specificity of the scales used). Further research is necessary in this field to be able to draw definitive conclusions.
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Activities of Daily Living , Dementia/diagnosis , Geriatric Assessment/methods , Aged , Aged, 80 and over , Dementia/psychology , Humans , Psychometrics , Sensitivity and SpecificityABSTRACT
OBJECTIVE: To validate the Seven-Minute Screen Neurocognitive Battery (7MS) in an elderly population-based sample to identify dementia using a new scoring method. METHODS: Five hundred and twenty-seven home-dwelling elderly were assessed with a neurological and neuropsychological exam. The total score of the 7MS was the sum of z scores of its subtests. Dementia was diagnosed according to DSM-IV. The ROC curve and the diagnostic parameters of the 7MS were calculated. RESULTS: The 7MS could be fully applied in 416 cases (78.9%), and 48 were diagnosed as demented independently of the 7MS. The four 7MS subtests correctly classified 97.6% of cases by discriminant analysis; orientation and memory were the most discriminative. Factorial analysis showed a single dimension in the 7MS. The ROC curve area for diagnosis of dementia was 0.996 (95% CI 0.992-1), sensitivity 100%, specificity 95.1%, and diagnostic accuracy 96.8%. All these parameters were higher than those of other cognitive screening tests. Dementia explained 54.9% of the variance of the 7MS, and age 3.1%; sex and education did not have a significant effect. CONCLUSIONS: The 7MS is a valid tool for the diagnosis of dementia, even when cognitive decline is mild, although it may not be appropriate for extensive epidemiological surveys.
Subject(s)
Dementia/diagnosis , Dementia/epidemiology , Neuropsychological Tests , Aged , Aged, 80 and over , Demography , Factor Analysis, Statistical , Female , Humans , Male , Mental Recall , Population Surveillance/methods , Reproducibility of Results , Severity of Illness Index , Spain/epidemiology , Time FactorsABSTRACT
BACKGROUND AND OBJECTIVE: To define the parameters of normal cognitive performance in an easy to administer neuropsychological battery of a Spanish population sample of elderly over 70 years. SUBJECTS AND METHOD: We examined 527 home dwelling elderly from the longitudinal study Envejecer en Leganés, 71 to 99 years old (mean age [SD] 79 [6.2] years, 51.8% women, 38.7% without formal education), with an extensive clinical survey, a neurological exam and the following neuropsychological battery: Short Portable Mental Status Questionnaire, Mini Mental State Examination, Benton Orientation Test, Bell Test, Verbal Fluency, Clock Drawing Test, Trail Making Test, Free and Cued Figures Recall, Logic Memory, Naming, incidental Recall, Delayed Recall, Similarities, IQCODE Questionnaire Of Jorm and Depression Questionnaire CES-D. 111 cases who rejected the assessment or had sensomotor limitations were excluded. 368 non demented subjects (according to DSM-IV criteria; 88.5% of the de 416 remaining cases) were selected to establish the normative data of every test. RESULTS: The analyzed subsample was representative of the total sample. The normative data for every neuropsychological test were obtained in the total group of non demented subjects and in the subgroups stratified by four age levels and two cultural levels. The mean values, standard deviations, range and percentiles for every test and subgroup are presented. CONCLUSIONS: The normative data obtained in this population sample for a neuropsychological battery easy to administer to poorly educated elderly can be useful to rigourously apply the criteria of dementia and mild cognitive impairment in future clinical and population studies.
Subject(s)
Cognition Disorders/diagnosis , Cognition , Neuropsychological Tests , Aged , Aged, 80 and over , Female , Humans , Male , Reference Values , Sampling Studies , SpainABSTRACT
AIM: To validate the 'Prueba Cognitiva de Leganés' (PCL) as a screening tool for cognitive impairment in elderly people with little formal education. METHODS: The PCL is a simple cognitive test with 32 items that includes two scores of orientation and memory and a global score of 0-32 points. It was applied to a population sample of 527 elderly people over 70 with low educational level, who were independently diagnosed by consensus between two neurologists as having normal cognitive function, age associated cognitive decline (AACD, IPA-OMS criteria) or dementia (DSM-IV criteria). Individuals with severe visual or hearing defects and those who rejected the exam were excluded from the study. The PCL was validated in a sample of 375 individuals: 300 normal, 42 with AACD and 33 with dementia. The sensitivity, specificity, accuracy and likelihood ratios, as well as the ROC curves for dementia and for AACD-dementia, were calculated. The confounding effect of sociodemographic variables was assessed by logistic regression analysis and convergent validity by partial correlations of the PCL with other cognitive tests. Inter-rater reliability was evaluated with the intraclass correlation coefficient. RESULTS: The PCL identified dementia (cut-off < or =22) and AACD-dementia (cut-off < or =26), with the following diagnostic parameters, respectively: sensitivity 93.9%-80%, specificity 94.7%-84.3%, positive likelihood ratio 17.8-5.1, negative likelihood ratio 0.06-0.24, and accuracy 94.6%-83.4%. The areas under the ROC curve were 0.985 (95% Confidence Intervals (CI) 0.967-0.995) and 0.904 (95% CI: 0.870-0.932) respectively. The intraclass correlation coefficient was 0.79 (0.74-0.83). CONCLUSION: The PCL is a simple instrument, which is both valid and reliable, for the screening of dementia in population samples of individuals with low educational level. This instrument could be useful in primary health care.