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Objectives: To determine whether videos taken by parents of their infants' spontaneous movements were in accordance with required standards in the In-Motion-App, and whether the videos could be remotely scored by a trained General Movement Assessment (GMA) observer. Additionally, to assess the feasibility of using home-based video recordings for automated tracking of spontaneous movements, and to examine parents' perceptions and experiences of taking videos in their homes.
Design: The study was a multi-centre prospective observational study.
Setting: Parents/families of high-risk infants in tertiary care follow-up programmes in Norway, Denmark and Belgium.
Methods: Parents/families were asked to video record their baby in accordance with the In-Motion standards which were based on published GMA criteria and criteria covering lighting and stability of smartphone. Videos were evaluated as GMA 'scorable' or 'non-scorable' based on predefined criteria. The accuracy of a 7-point body tracker software was compared with manually annotated body key points. Parents were surveyed about the In-Motion-App information and clarity.
Participants: The sample comprised 86 parents/families of high-risk infants.
Results: The 86 parent/families returned 130 videos, and 121 (96%) of them were in accordance with the requirements for GMA assessment. The 7-point body tracker software detected more than 80% of body key point positions correctly. Most families found the instructions for filming their baby easy to follow, and more than 90% reported that they did not become more worried about their child's development through using the instructions.
Conclusions: This study reveals that a short instructional video enabled parents to video record their infant's spontaneous movements in compliance with the standards required for remote GMA. Further, an accurate automated body point software detecting infant body landmarks in smartphone videos will facilitate clinical and research use soon. Home-based video recordings could be performed without worrying parents about their child's development.
Trials Registration Number: NCT03409978.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934716 | PMC |
http://dx.doi.org/10.1136/bmjopen-2020-042147 | DOI Listing |
Cureus
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Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, JPN.
Pharyngeal myoclonus is a rare movement disorder characterized by rhythmic pharyngeal contractions, typically reported in adults with neurological lesions and rarely in children. We report a seven-year-old girl who experienced involuntary clicking sounds localized to the right ear. Nasopharyngoscopy revealed pharyngeal myoclonus without structural abnormalities, and brain and laryngeal MRI were unremarkable.
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September 2025
Department of Medicine, Huddinge, Karolinska Institutet, 141 83, Huddinge, Sweden.
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Carotid-cavernous fistulas (CCF) are indirect or direct vascular shunts between vessels of the cavernous sinus and the carotid artery. While indirect CCFs have high rates of spontaneous resolution, direct CCF cases can result in significant orbital and neurological sequelae. This case describes a 75-year-old male patient presenting with acute subarachnoid hemorrhage secondary to a Barrow type-D CCF.
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September 2025
Department of Rehabilitation, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center; Nijmegen, the Netherlands; Department of Research, Sint Maartenskliniek, Nijmegen, the Netherlands.
Introduction: Multi Sensory Stimulation And Priming (MuSSAP) is an early upper limb training for infants at high risk of unilateral cerebral palsy (CP). MuSSAP is designed to enhance awareness of the affected upper limb facilitating initiation of goal-directed movements. This study assesses the effectiveness of an 8-week MuSSAP training on manual ability in a clinical setting.
View Article and Find Full Text PDFClin Transl Gastroenterol
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Lynda K and David M Underwood Center for Digestive Health, Houston Methodist, Houston, TX, USA.
Introduction: Pharmacological therapies for chronic idiopathic constipation (CIC) are useful, but many patients report dissatisfaction from a lack of efficacy and occurrence of adverse events. The vibrating capsule (VC) is an FDA approved non-pharmacologic, treatment for CIC. However, its long-term usefulness in a community setting is unknown.
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