Perspectives, Directions and New Frontiers for Research and Clinical Practice in Pediatric Psychology

A special issue of Pediatric Reports (ISSN 2036-7503). This special issue belongs to the section "Pediatric Psychology".

Deadline for manuscript submissions: closed (30 April 2023) | Viewed by 3490

Special Issue Editors


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Guest Editor
Department of Psychology, Educational Science and Human Movement (SPPEFF), University of Palermo, 90100 Palermo, Italy
Interests: pediatric psychology; child neglect; pediatric onco-hematology conditions: risk factors and evolutionary resources; parental competence; evolutionary assessment; risk pregnancies; preterm birth: maternal and infant health

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Guest Editor
Department of Psychology, Educational Science and Human Movement (SPPEFF), University of Palermo, 90100 Palermo, Italy
Interests: pediatric psychology and maternal child health; medically assisted procreation; preterm birth; high-risk pregnancies; chronic and acute pathologies; psycho-traumatology; best practices on integrated intervention and psychological support in healthcare organizations; child neglect

Special Issue Information

Dear Colleagues,

This Special Issue—as highlighted on the international level by the scientific contributions of the 54th Division of the American Psychological Association and on the national level by the commitment of the Italian Society of Pediatric Psychology—begins with the consideration that research and intervention in pediatric psychology present numerous aspects of complexity (with respect to focus, perspectives, methods and methodologies, tools, etc.), which are related to the same complexity of the know-how of this discipline and consequently of the same object of study, requiring new openings for an increasing number of interdisciplinary contributions.

Pediatric psychology, as an evolutionary–clinical branch of psychology, assumes the following as objects of study and intervention: evolutionary processes in conditions characterized by the presence of a chronic or rare disease, a congenital malformation, disability, prematurity, etc., from the prenatal period, and conditions of the child/adolescent that constitute real conditions of "evolutionary emergency" with clinical and social implications. In this sense, pediatric psychology is of great interest to researchers, clinicians and the whole reference community of health in the pediatric and maternal–infant field. Shifting according to pediatric psychology implies orienting research towards the study of evolutionary resources even before compromises are oriented by disease/disability, recovering the most innovative perspectives on development, such as that of evolutionary trajectories and the contribution of neuroscience and epigenetic perspective, and not losing sight of the possible relationships between medical, psychological and social variables. Along with these aspects of complexity, the need for functional research to identify best practices for the promotion of well-being, understood as health (including mental health) in pediatric conditions must also be considered. In this sense, it is often research that identifies with assessment; on the level of the intervention, it appears relevant to move according to an integrated cure–care approach, which today is identified in the concept of "taking charge" as a process of care that crosses the dimensions/conditions of listening, welcoming, supporting, etc. Additionally, again, in pediatric psychology, attention to research and intervention with the family and systems of care (a medical team of reference) must be emphasized as the key leaders in the field of relationships that define every pediatric condition. Considering this framework and the complexity indicated, and accounting for the fact that the research contributions of pediatric psychology are often not clearly defined or collocated on the level of the indicated background, this Special Issue aims to promote the knowledge of research and action-research conducted according to this know-how among researchers, clinicians and young people in training interested in pediatric psychology. This is research that can be functional in improving the management of pediatric conditions in healthcare and prevention, hospital and territorial contexts. Through original articles, reviews, short communications and correspondence regarding all the relevant themes and topics of pediatric psychology, the aim is to highlight the richness of the possible directions of this research, but also the possible limits and future perspectives.

Prof. Dr. Concetta Polizzi
Prof. Dr. Giovanna Perricone
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Pediatric Reports is an international peer-reviewed open access quarterly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 1600 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • pediatric oncohematology
  • pediatric pain
  • preterm birth
  • risk pregnancies
  • child neglect
  • parental competence in pediatric condition
  • promotion of psychological well-being for mother and infant
  • children with disability
  • development assessment
  • medically assisted procreation
  • best practices in pediatric psychology

Published Papers (2 papers)

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Research

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11 pages, 255 KiB  
Article
No Child Should Be Left Behind by COVID-19: A Report about the COVID-19 Pandemic Experience in Children and Adolescents with Acute or Chronic Disease Treated at a Pediatric Referral Hospital in Italy
by Giulia Zucchetti, Sabrina Ciappina, Cristiana Risso, Alice Malabaila, Sara Racalbuto, Elena Longo, Margherita Dionisi Vici, Marina Bertolotti, Paola Quarello and Franca Fagioli
Pediatr. Rep. 2023, 15(1), 58-68; https://doi.org/10.3390/pediatric15010008 - 28 Jan 2023
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Abstract
Background: The pandemic of coronavirus disease 2019 (COVID-19) was undoubtedly a stressful experience for everyone. General opinion believed that children with acute or chronic illness could experience additional burden, but this is not confirmed. The aim of this study is to understand how [...] Read more.
Background: The pandemic of coronavirus disease 2019 (COVID-19) was undoubtedly a stressful experience for everyone. General opinion believed that children with acute or chronic illness could experience additional burden, but this is not confirmed. The aim of this study is to understand how children and adolescents already suffering from acute or chronic illness (e.g., cancer, cystic fibrosis, neuropsychiatric disorders) feel about the COVID-19 pandemic, and if the experience is significantly different between these children and children without illness. Methods: Children and adolescents affected by acute or chronic illness (named the “fragile group”) treated at the Regina Margherita Children Hospital in Italy, were enrolled in the study by filling a questionnaire about their pandemic experiences. Also, a group of children and adolescents without acute or chronic illness (named the “low-risk group”) recruited in the emergency department of the hospital, participated in the study in order to compare experiences. Results: The study group was composed of 166 children and adolescents (Median age = 12 yrs; 78% fragile group, 22% low-risk group). Participants experienced a general state of fear of the virus and of a potential infection for both themselves and their families, while feelings and thoughts that interfere with daily functioning were less frequent. The fragile group seems to be more resilient towards the pandemic situation than low-risk group and some differences on the basis of the type of illness were found in the fragile group. Conclusions: Dedicated psychosocial intervention must be proposed in order to support fragile children and adolescents’ well-being during the pandemic, also on the basis of their clinical and mental history. Full article

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11 pages, 596 KiB  
Case Report
Early Introduction of Power Mobility Devices for Children with Fukuyama Congenital Muscular Dystrophy and Its Psychological Impact on Caregivers: A Case Report
by Hitomi Fujita
Pediatr. Rep. 2023, 15(3), 403-413; https://doi.org/10.3390/pediatric15030037 - 05 Jul 2023
Cited by 1 | Viewed by 1445
Abstract
Recently, motorized mobility devices (or power mobility devices (PMDs)) have been introduced for infants and toddlers who lack the means for self-mobility. Previous reports have primarily focused on PMDs for individuals with cerebral palsy. Few have explored PMDs for individuals with neuromuscular diseases [...] Read more.
Recently, motorized mobility devices (or power mobility devices (PMDs)) have been introduced for infants and toddlers who lack the means for self-mobility. Previous reports have primarily focused on PMDs for individuals with cerebral palsy. Few have explored PMDs for individuals with neuromuscular diseases who have intellectual disabilities. This report presents a case study of the early introduction of a PMD for an infant with Fukuyama congenital muscular dystrophy and presents the results of an interview with the father regarding psychological aspects and the child’s manipulative abilities. The PMD was introduced at the age of 1 year and 10 months, and the changes during the 19 months after the introduction were evaluated six times, using the Assessment of Learning Powered mobility use tool (ALP). A semi-structured interview with the father was conducted 19 months after the introduction. The ALP evaluation and the interview were conducted by one physical therapist and two physical therapy students, and the results were shared with the hospital’s physical therapist and nurses at the nursing facility. This report provides a basis for expanding the scope of PMD use and for considering the family’s involvement, especially for the child. Full article
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