Evidence map›Paper›PMID 41627073›Full record

ArticleJournal of neuromuscular diseases2026

Active-NDM: Development of a patient-reported outcome questionnaire to measure the impact of non-dystrophic myotonia on activity of daily living.

Ahmed Amara, Michele Cavalli, Andra Ezaru, Angela Puma, Jérémy Garcia, Sophie Meiran, Aurora Parrotta, Savine Vicart, Yann Péréon, Emmanuelle Salort-Campana and 4 more

Registry-linked trialAbstract read
In one paragraph

Article in Journal of neuromuscular diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06136416 (Pilot Study for the Development of an Activity and Quality of Life Questionnaire for the Follow-up of Patients With Non-dystrophic Myotonia), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

NCT06136416 nacompletednot on this map

Pilot Study for the Development of an Activity and Quality of Life Questionnaire for the Follow-up of Patients With Non-dystrophic Myotonia

TypeinterventionalSponsorCentre Hospitalier Universitaire de NiceRan2024 to 2024Enrolled10ConditionsNon-Dystrophic MyotoniaArmsQuestionnaire for Non-dystrophic myotonias
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Ahmed AmaraPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Michele CavalliPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Andra EzaruPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Angela PumaPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Jérémy GarciaPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Sophie MeiranPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.
Aurora ParrottaPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.ORCID 0009-0002-8176-0679
Savine VicartNational Muscle Channelopathies Reference Center, Service of Neuro-Myology, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Pitié-Salpêtrière University Hospital, Paris, France.ORCID 0000-0002-0101-4098
Yann PéréonDepartment of Clinical Neurophysiology, Reference Centre for Neuromuscular Diseases AOC, Filnemus, Euro-NMD, CHU Nantes, Nantes Université, Place Alexis-Ricordeau, Nantes, France.ORCID 0000-0002-0090-3571
Emmanuelle Salort-CampanaReference Center for Neuromuscular Diseases and ALS, CHU La Timone, Marseille, France.
Martin MoussyHôpital Neurologique Pierre Wertheimer, Service d'ENMG et de Pathologies neuromusculaires, centre de référence des maladies neuromusculaires PACA-Réunion-Rhône Alpes, Hospices Civils de Lyon, Groupement Est, 59 Boulevard Pinel, Bron, France.
Aleksandra Nadaj-PaklezaNeurology Department, Reference Center for Neuromuscular Diseases, Strasbourg University Hospitals, Strasbourg, France.
Rocio Nur Villar-QuilesNational Muscle Channelopathies Reference Center, Service of Neuro-Myology, Assistance Publique-Hôpitaux de Paris, Sorbonne Université, Pitié-Salpêtrière University Hospital, Paris, France.ORCID 0000-0001-6706-3506
Sabrina SacconiPeripheral Nervous System & Muscle Department, Reference Center for Neuromuscular Disorders, Pasteur 2 Hospital, Nice University Hospital, Nice, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a considerable challenge in managing non-dystrophic myotonias (NDM), due to the lack of gold-standard outcome measures to assess NDM burden on activities of daily living and quality of life from the patient's perspective.

objectiveIn this study, we aim to develop and validate a specific NDM patient-reported outcome (PRO) questionnaire.

methodsThe Active-NDM questionnaire was developed through a modified 2-round Delphi procedure integrating feedback from stakeholders and a systematic literature review, with input from 11 national clinical experts. The questionnaire was validated in a pilot study of 10 patients with NDM. Both clinical experts and patients assessed questions for pertinence/relevance and clarity. We excluded questions that were not considered pertinent/relevant, and reformulated any judged to be poorly formulated, by >80% of the experts/patients. We also excluded questions with <80% reproducibility during the pilot study.

resultsBased on feedback from experts and findings of the systematic literature review, we identified 130 questions, of which 100 were unduplicated. During the Delphi process, we removed 66 questions due to lack of pertinence and/or relevance. In the pilot study, patients with NDM evaluated the resulting 34-questions for pertinence, clarity, and reproducibility. Subsequently we removed 9 questions that did not achieve the required level of reproducibility.

conclusionWe developed the Active-NDM questionnaire, composed by 25 questions, figuring as a new NDM-specific measure to determine the impact of the disease on patients' activities of daily living and quality of life. Active-NDM could be a valuable tool in the management of patients with NDM. These findings should be interpreted as preliminary. Larger-scale validation studies are warranted to confirm the tool's psychometric properties and generalizability. CLINICALTRIALS: gov identifier: NCT06136416.

Indexed as

activities of daily livingDelphi processmyotonia congenitanon dystrophic myotoniasparamyotonia congenitapatient reported outcome measuresquality of life

Identifiers

PMID41627073
PMCPMC13438962

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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.