Publications by authors named "Julie M Orlando"

Purpose: Evaluate the content and variability of infant motor milestone education provided to parents in popular sources.

Methods: Sources were screened for inclusion, and their motor milestone content was coded. Descriptive and inferential analyses were performed.

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Purpose: Containers (eg, strollers, bouncers) are an important part of infants' environment but may negatively impact infant development and health. This study evaluated movement and play opportunities, constraints, and manufacturers' developmental claims for infant containers.

Methods: Containers were identified through Amazon.

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Aim: Systematically evaluate the depth and quality of play recommendations provided in popular sources for parents of infants in the first year of life.

Methods: This represents the second stage of a larger analysis of educational content available to parents. Two coders (>90% agreement) extracted and coded play activities from popular websites, applications, and books screened from a systematic online search.

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Parents commonly seek information about infant development and play, yet it is unclear what information parents find when looking in popular sources. Play, Milestone, and Development Searches in Google identified 313 sources for content analysis by trained researchers using a standardized coding scheme. Sources included websites, books, and apps created by professional organizations, commercial entities, individuals, the popular press, and government organizations/agencies.

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Background: Parents utilize online sources to learn about health information, however few studies have examined where parents look for information about development or play for young children.

Aims: Investigate parents' and early intervention (EI) providers' practices and preferences regarding parent education about infant development and play.

Study Design: Cross-sectional survey design.

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Purpose: Develop and initially evaluate a soft ankle support (SAS) garment for children with ankle impairments.

Description Of Cases: Two participants were evaluated at baseline and interviews with their parent(s) to identify wants and needs for the SAS. The SAS was developed and evaluated via participant report and functional measures in barefoot, ankle-foot orthosis (AFO), and SAS conditions.

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Objective: To systematically review perceptions from adults, children, and caregivers in scientific and open sources to determine how well lower extremity orthotic devices (LEODs) meet users' functional, expressive, aesthetic, and accessibility (FEA2) needs.

Data Sources: Scientific source searches were conducted in the National Library of Medicine (PubMed/MEDLINE) and Web of Science; open source searches were conducted in Google Search Engine in April 2020.

Study Selection: Inclusion criteria were reporting of users' perceptions about a LEOD, experimental or observational study design, including qualitative studies, and full text in English.

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This article presents strategies for reframing clinical paradigms to build better therapeutic relationships with patients and the members of their support network from the unique and important lens of a parent and disability researcher. First, a brief history of the evolution of models of care is presented, and implementation of the current biopsychosocial model is discussed. Then, evidence-based practice and the role of the patient perspective is considered.

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Background: Children with cerebral palsy are less likely to be physically active than their peers, however there is limited evidence regarding self-initiated physical activity in toddlers who are not able, or who may never be able, to walk.

Aims: The aim of this study was to measure self-initiated physical activity and its relationship to gross motor function and participation in non-ambulatory toddlers with cerebral palsy.

Methods And Procedures: Participants were between the ages of 1-3 years.

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