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Purpose Of Review: Parent-implemented autism interventions are considered empirically validated interventions and the use of telepractice in these interventions is reported as effective. However, little is known about the social validity assessments and outcomes of these interventions. The purpose of this review is to explore the current practices of conducting social validity assessment and reporting its outcomes within parent-implemented telepractice autism interventions.
Recent Findings: The 11 reviewed studies included caregivers as participants, telepractice intervention focusing on social communication outcomes of young autistic children, and were published in a peer-reviewed journal within the past five years.
Summary: The researchers in the reviewed articles reported positive outcomes for parent-implemented telepractice autism interventions. Notably, however, information about social validity assessments of the interventions was limited. Researchers are encouraged to evaluate the social validity of interventions using multiple data sources and methods, and report on their findings as they relate to other types of data.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640782 | PMC |
http://dx.doi.org/10.1007/s40474-022-00259-z | DOI Listing |
J Healthc Sci Humanit
January 2024
Bioethics Honors Student.
Efforts to reduce the unequal impacts and generations of systemic disadvantage and inequality in healthcare for black and brown communities became amplified and were made more urgent during the COVID-19 pandemic. Moreover, public health surveillance systems have been challenged to address the vulnerabilities that residents within these environments and experiences. This paper describes the methodology used to develop a public health ethics and bioethics surveillance system grounded in empathy and care ethics.
View Article and Find Full Text PDFAddict Behav Rep
June 2025
Department of Psychiatry, Yale University School of Medicine, New Haven, CT, USA.
This article proposes minimum requirements for reporting efficacy in treatment studies of compulsive sexual behavior (CSB). CSB disorder (CSBD) is a condition whose diagnostic criteria were only recently defined by the World Health Organization. Multiple primary and secondary outcomes have been used in treatment trials of CSB, and possible neuropsychological measures have been considered.
View Article and Find Full Text PDFCancer Manag Res
September 2025
Department of Pain, The First People's Hospital of Zunyi City, Zunyi, Guizhou, 563000, People's Republic of China.
Objective: To evaluate the effects of a comprehensive intervention program on cancer pain and self-efficacy in patients with lung cancer.
Methods: A total of 120 lung cancer patients with cancer pain who received treatment from January 2021 to December 2023 at The First People's Hospital of Zunyi were enrolled in this study. A within-subject design was used, comparing patients' pain and self-efficacy scores before and after a comprehensive intervention.
Front Public Health
September 2025
Department of Health Care Sciences, Marie Cederschiöld University, Stockholm, Sweden.
Purpose: This study investigates how older foreign-born adults in Sweden experience and navigate social connectedness as a determinant of wellbeing.
Methods: Employing Glaser's grounded theory methodology, we collected qualitative data through individual ( = 1) and focus group ( = 5) interviews with 23 participants aged 60 + representing four distinct cultural-linguistic groups: Arabic, Finnish, Spanish, and Chinese speakers.
Results: The analysis identified "" as the core category, encompassing three dimensions: (1) , (2) , and (3) .
Cureus
August 2025
Department of Pediatrics, Mohammed VI University Hospital, Faculty of Medicine and Pharmacy, Mohammed I University, Oujda, MAR.
Objective: Celiac disease (CD) requires a lifelong gluten-free diet, which impacts the health-related quality of life (HRQoL) of children. To better understand this impact, our study evaluated the HRQoL of children diagnosed with CD and followed at the University Hospital Center (CHU) of Oujda using the Arabic-validated version of the Coeliac Disease Dutch Questionnaire (CDDUX).
Methods: A cross-sectional study included 49 children with CD, aged 8 to 18 years, and their parents.