Evidence map›Paper›PMID 42174309›Full record

ArticleCerebellum (London, England)2026

A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

Maresa Buchholz, Victoire Monier, Claire Ewenczyk, Anna Heinzmann, Lucie Pierron, Sabrina Sayah, Rania Hilab, Mariana Atencio, Elodie Petit, Fanny Bertrand and 23 more

Registry-linked trialAbstract read
In one paragraph

Article in Cerebellum (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05943002 (Patient-reported, Health Economic and Psychosocial Outcomes in Friedreich Ataxia), which is not on this map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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.

NCT05943002 recruitingnot on this map

Patient-reported, Health Economic and Psychosocial Outcomes in Friedreich Ataxia

TypeobservationalSponsorGerman Center for Neurodegenerative Diseases (DZNE)Ran2023 to 2028Enrolled200ConditionsFriedreich Ataxia
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

33 authors.

Maresa BuchholzGerman Center for Neurodegenerative Diseases, Patient-reported Outcomes & Health Economics Research, Site Rostock/Greifswald, Greifswald, Germany.ORCID http://orcid.org/0000-0002-4486-8632
Victoire MonierSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.
Claire EwenczykSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-4864-6287
Anna HeinzmannSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0001-8522-7199
Lucie PierronSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-2888-3226
Sabrina SayahSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-0382-9995
Rania HilabSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0009-0002-6310-2066
Mariana AtencioSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0009-0000-3574-0728
Elodie PetitSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0009-0008-7016-9908
Fanny BertrandSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.
Alix VallancienSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.
Chloé DiotSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.
Stéphan RouillonAssociation Française de l'Ataxie de Friedreich, Hirson, France.
Andreas NadkeDeutsche Heredo-Ataxie-Gesellschaft, Stuttgart, Germany.
Katrin FeldmannGerman Center for Neurodegenerative Diseases, Bonn, Germany.
Vivian MaasGerman Center for Neurodegenerative Diseases, Bonn, Germany.
Jennifer FaberGerman Center for Neurodegenerative Diseases, Bonn, Germany.ORCID http://orcid.org/0000-0003-3265-0262
Dorota SarwinskaGerman Center for Neurodegenerative Diseases, Patient-reported Outcomes & Health Economics Research, Site Rostock/Greifswald, Greifswald, Germany.ORCID http://orcid.org/0000-0002-7592-0544
Sylvia M BoeschCenter for rare Movement Disorders Innsbruck, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-1657-7368
Elisabetta IndelicatoCenter for rare Movement Disorders Innsbruck, Department of Neurology, Medical University Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-0217-8630
Almut T BischoffDepartment of Neurology, Friedrich-Baur-Institute, LMU University Hospital, Ludwig- Maximilians-Universität (LMU), Munich, Germany.
Thomas KlopstockDepartment of Neurology, Friedrich-Baur-Institute, LMU University Hospital, Ludwig- Maximilians-Universität (LMU), Munich, Germany.ORCID http://orcid.org/0000-0003-2805-4652
Jörg B SchulzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Kathrin ReetzDepartment of Neurology, RWTH Aachen University, Aachen, Germany.
Zofia FleszarDepartment of Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.
Audrey IskandarGerman Center for Neurodegenerative Diseases, Patient-reported Outcomes & Health Economics Research, Site Rostock/Greifswald, Greifswald, Germany.ORCID http://orcid.org/0009-0007-6400-507X
Thomas KlockgetherGerman Center for Neurodegenerative Diseases, Bonn, Germany.ORCID http://orcid.org/0000-0001-6174-5442
Marcus Grobe-EinslerGerman Center for Neurodegenerative Diseases, Bonn, Germany.
Feng XieDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
Brittany HumphriesDepartment of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Ontario, Canada.
Bernhard MichalowskyGerman Center for Neurodegenerative Diseases, Patient-reported Outcomes & Health Economics Research, Site Rostock/Greifswald, Greifswald, Germany.ORCID http://orcid.org/0000-0002-3425-0089
Alexandra DurrSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France.ORCID http://orcid.org/0000-0002-8921-7104
Stéphanie BorelSorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, CNRS, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université, Paris, France. stephanie.borel@icm-institute.org.ORCID http://orcid.org/0000-0002-8597-9937

Funding

Agence Nationale de la Recherche ANR21-RAR4-0003-04);Bundesministerium für Ernährung und Landwirtschaft 01GM2110EJP RD 825575
6 · The paper itself

Abstract

BACKGROUND AND

objectivesFriedreich ataxia (FA) causes progressive impairment of communication due to gradual deterioration of speech, associated with impaired hearing, socio-cognitive and language skills. There is an urgent need to investigate the impact of this multiparametric alteration on patients' lives. Therefore, the COMunication and ATAXia measure (COMATAX) was developed and validated in French and German.

methodsIn the PROFA study (NCT05943002), we conducted focus groups and cognitive interviews with patients with FA, professionals and caregivers to elaborate relevant items of communication disabilities. Subsequently, the measure was validated in 93 patients with FA via a mobile health app. For validation, distribution properties, reliability (Cronbach's alpha) and validity (correlations with VHI-30, SSQ-12, SARA total score, SARA speech item, Speech rate and GAA repeats; known-groups validity by age, sex, and self-rated health/wellbeing, disease-severity, hearing function, daily activities, and exploratory factor analysis) were calculated. An IRT analysis was performed to assess item characteristics.

resultsCOMATAX consists of 17 items (five response options each) and an 18th question asking about the most bothersome symptom. We observed high internal consistency for the total COMATAX scale (α = 0.897), strong correlations with VHI-30 (r=.894), SSQ-12 (r = -.531), moderate with SARA score (r=.498), SARA speech item (r=.416), Speech rate (r=-.354), weak with GAA repeat length (r

conclusionThe COMATAX is a valid and reliable patient-reported communication disability measure, useful in future therapeutic trials in FA.

Indexed as

Communication DisordersFriedreich AtaxiaPatient Reported Outcome MeasuresAdolescentAdultFemaleHumansMaleMiddle AgedReproducibility of ResultsYoung AdultAtaxiaCerebellar cognitive affective syndromeCommunicationHearingPatient-related outcome measureSpeech

Identifiers

PMID42174309
PMCPMC13197451

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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.