ArticleMuscle & nerve2021
Walking activity in a large cohort of boys with Duchenne muscular dystrophy.
Article in Muscle & nerve, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01484678 (Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy), which is not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy
Who cites it
13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.
- The use of digital outcome measures in clinical trials in rare neurological diseases: a systematic literature review.Orphanet journal of rare diseases · 2023Pooled it
- Advancements from the EVOLVE study for assessing real-world experience with eteplirsen, golodirsen and casimersen for the treatment of DMD.Journal of comparative effectiveness research · 2026Trial
- Home-based exercise training in boys with Duchenne muscular dystrophy: A 12-month intervention study.Journal of pediatric rehabilitation medicine · 2026Article
- Using wearable sensors during the timed up and go and 6-minute walk test in Spinal Bulbar Muscular Atrophy.PLOS digital health · 2026Article
- Digital outcome measures in Duchenne muscular dystrophy: Lessons learnt from clinical trials.Journal of neuromuscular diseases · 2026Review
- Evaluation of a control paradigm allowing heart rate guided rehabilitative exercise for boys with Duchenne muscular dystrophy.Journal of neuroengineering and rehabilitation · 2025Article
- Wearable sensors in paediatric neurology.Developmental medicine and child neurology · 2025Review
- Cardiopulmonary exercise testing as an integrative approach to explore physiological limitations in Duchenne muscular dystrophy.Journal of neuromuscular diseases · 2025Article
- Unveiling the Respiratory Muscle Strength in Duchenne Muscular Dystrophy: The Impact of Nutrition and Thoracic Deformities, Beyond Spirometry.Children (Basel, Switzerland) · 2024Article
- Gait Characterization in Duchenne Muscular Dystrophy (DMD) Using a Single-Sensor Accelerometer: Classical Machine Learning and Deep Learning Approaches.Sensors (Basel, Switzerland) · 2024Article
- Spirometry correlates with physical activity in patients with Duchenne muscular dystrophy.Pediatric pulmonology · 2023Article
- How is Physical Activity Measured in Spinal Muscular Atrophy and Duchenne Muscular Dystrophy?Journal of neuromuscular diseases · 2023Review
- Step Activity Monitoring in Boys with Duchenne Muscular Dystrophy and its Correlation with Magnetic Resonance Measures and Functional Performance.Journal of neuromuscular diseases · 2022Article
Corrections and comments
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Authors and funding
12 authors at 6 institutions in 1 country.
Funding
Abstract
introductionIn this study we explored walking activity in a large cohort of boys with Duchenne muscular dystrophy (DMD).
methodsStep activity (monitored for 7 days), functional ability, and strength were quantified in ambulatory boys (5-12.9 years of age) with DMD and unaffected boys. Ambulatory status was determined 2 years later.
resultsTwo to 5 days of activity monitoring predicted weekly step activity (adjusted R DISCUSSION: Step activity for DMD is related to and predictive of functional declines, which may be useful for clinical trials.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.