J. Hogrel , R. Muni-Lofra , P. Santmarty , V. Decostre , T. Marques , E. Haf Davies , V. Straub , the DT4RD Project Group
{"title":"211P 跟踪病人在日常生活中的行动能力:EJP-DT4RD 项目","authors":"J. Hogrel , R. Muni-Lofra , P. Santmarty , V. Decostre , T. Marques , E. Haf Davies , V. Straub , the DT4RD Project Group","doi":"10.1016/j.nmd.2024.07.062","DOIUrl":null,"url":null,"abstract":"<div><div>The DT4RD (Digital Tools 4 Rare Diseases) project is dedicated to the development of a non-invasive toolbox that measures patient mobility in daily life. Although tremendous progress has been made in this regard in the last few years, there is still a strong need to obtain disease-related information that generates fundamental clinical and patient-relevant outcomes accepted by regulators. Such data can be harnessed through digitised means using tools such as wearable devices, sensors, videos and smartphone apps. For example, movement sensors in the patient's home, worn on the body, or mobility aid can assess general movements whilst distinguishing between the patient's voluntary and involuntary actions. The development of novel clinical outcome assessments (COA) has the potential to facilitate the drug development process across rare diseases and support the improvement of the quality of life for patient care, clinical outcomes and ability to collect information in the home environment. The remote evaluation of patient movements can also reduce indirect costs, such as travel to study sites and lost wages, thereby increasing the accessibility of research studies for patients. The aim of this study is to compare hospital-based COAs with home-based COAs to validate their use for remote monitoring of patients. The recruitment target is 40 patients with confirmed diagnosis of a neuromuscular condition. Participants will be followed for one year with three hospital visits and regular recordings at home. We will present preliminary results obtained from 12 patients followed for six months. This project gives the possibility to question the classical ways of obtaining information from patients and creates new opportunities for acquiring patient-centred real data in daily life. Home monitoring provides a scientifically advanced approach to mobility assessment in clinical trials. By offering objective, continuous, and real-world monitoring of mobility parameters, it enhances data quality, ecological validity, and patient engagement. The integration of home monitoring technologies in clinical trial designs can revolutionise the assessment of mobility outcomes, leading to more accurate and meaningful insights into patients' mobility abilities, changes, and responses to interventions. The DT4RD program is funded by a grant from the European Joint Programme on Rare Diseases and co-funded by Chiesi and CSL Behring.</div></div>","PeriodicalId":19135,"journal":{"name":"Neuromuscular Disorders","volume":"43 ","pages":"Article 104441.53"},"PeriodicalIF":2.7000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"211P Following patient mobility in daily life: the EJP-DT4RD project\",\"authors\":\"J. Hogrel , R. Muni-Lofra , P. Santmarty , V. Decostre , T. Marques , E. Haf Davies , V. Straub , the DT4RD Project Group\",\"doi\":\"10.1016/j.nmd.2024.07.062\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The DT4RD (Digital Tools 4 Rare Diseases) project is dedicated to the development of a non-invasive toolbox that measures patient mobility in daily life. Although tremendous progress has been made in this regard in the last few years, there is still a strong need to obtain disease-related information that generates fundamental clinical and patient-relevant outcomes accepted by regulators. Such data can be harnessed through digitised means using tools such as wearable devices, sensors, videos and smartphone apps. For example, movement sensors in the patient's home, worn on the body, or mobility aid can assess general movements whilst distinguishing between the patient's voluntary and involuntary actions. The development of novel clinical outcome assessments (COA) has the potential to facilitate the drug development process across rare diseases and support the improvement of the quality of life for patient care, clinical outcomes and ability to collect information in the home environment. The remote evaluation of patient movements can also reduce indirect costs, such as travel to study sites and lost wages, thereby increasing the accessibility of research studies for patients. The aim of this study is to compare hospital-based COAs with home-based COAs to validate their use for remote monitoring of patients. The recruitment target is 40 patients with confirmed diagnosis of a neuromuscular condition. Participants will be followed for one year with three hospital visits and regular recordings at home. We will present preliminary results obtained from 12 patients followed for six months. This project gives the possibility to question the classical ways of obtaining information from patients and creates new opportunities for acquiring patient-centred real data in daily life. Home monitoring provides a scientifically advanced approach to mobility assessment in clinical trials. By offering objective, continuous, and real-world monitoring of mobility parameters, it enhances data quality, ecological validity, and patient engagement. The integration of home monitoring technologies in clinical trial designs can revolutionise the assessment of mobility outcomes, leading to more accurate and meaningful insights into patients' mobility abilities, changes, and responses to interventions. The DT4RD program is funded by a grant from the European Joint Programme on Rare Diseases and co-funded by Chiesi and CSL Behring.</div></div>\",\"PeriodicalId\":19135,\"journal\":{\"name\":\"Neuromuscular Disorders\",\"volume\":\"43 \",\"pages\":\"Article 104441.53\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Neuromuscular Disorders\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0960896624002268\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neuromuscular Disorders","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0960896624002268","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
211P Following patient mobility in daily life: the EJP-DT4RD project
The DT4RD (Digital Tools 4 Rare Diseases) project is dedicated to the development of a non-invasive toolbox that measures patient mobility in daily life. Although tremendous progress has been made in this regard in the last few years, there is still a strong need to obtain disease-related information that generates fundamental clinical and patient-relevant outcomes accepted by regulators. Such data can be harnessed through digitised means using tools such as wearable devices, sensors, videos and smartphone apps. For example, movement sensors in the patient's home, worn on the body, or mobility aid can assess general movements whilst distinguishing between the patient's voluntary and involuntary actions. The development of novel clinical outcome assessments (COA) has the potential to facilitate the drug development process across rare diseases and support the improvement of the quality of life for patient care, clinical outcomes and ability to collect information in the home environment. The remote evaluation of patient movements can also reduce indirect costs, such as travel to study sites and lost wages, thereby increasing the accessibility of research studies for patients. The aim of this study is to compare hospital-based COAs with home-based COAs to validate their use for remote monitoring of patients. The recruitment target is 40 patients with confirmed diagnosis of a neuromuscular condition. Participants will be followed for one year with three hospital visits and regular recordings at home. We will present preliminary results obtained from 12 patients followed for six months. This project gives the possibility to question the classical ways of obtaining information from patients and creates new opportunities for acquiring patient-centred real data in daily life. Home monitoring provides a scientifically advanced approach to mobility assessment in clinical trials. By offering objective, continuous, and real-world monitoring of mobility parameters, it enhances data quality, ecological validity, and patient engagement. The integration of home monitoring technologies in clinical trial designs can revolutionise the assessment of mobility outcomes, leading to more accurate and meaningful insights into patients' mobility abilities, changes, and responses to interventions. The DT4RD program is funded by a grant from the European Joint Programme on Rare Diseases and co-funded by Chiesi and CSL Behring.
期刊介绍:
This international, multidisciplinary journal covers all aspects of neuromuscular disorders in childhood and adult life (including the muscular dystrophies, spinal muscular atrophies, hereditary neuropathies, congenital myopathies, myasthenias, myotonic syndromes, metabolic myopathies and inflammatory myopathies).
The Editors welcome original articles from all areas of the field:
• Clinical aspects, such as new clinical entities, case studies of interest, treatment, management and rehabilitation (including biomechanics, orthotic design and surgery).
• Basic scientific studies of relevance to the clinical syndromes, including advances in the fields of molecular biology and genetics.
• Studies of animal models relevant to the human diseases.
The journal is aimed at a wide range of clinicians, pathologists, associated paramedical professionals and clinical and basic scientists with an interest in the study of neuromuscular disorders.