Evidence map›Paper›PMID 40332679›Full record

ArticleCerebellum (London, England)2025

Selection of Clinical Outcome Assessments for Trial Readiness in ARSACS - 2-year Progression and Responsiveness to Change Part 2: Mobility, Balance, and Lower Limb Coordination.

Isabelle Lessard, Elise Duchesne, Luc J Hébert, Bernard Brais, Xavier Rodrigue, François Routhier, Krista Best, Jean-Denis Brisson, Florentin Thullier, Sébastien Gaboury and 2 more

Abstract read
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In one paragraph

Article in Cerebellum (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

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

12 authors.

Isabelle LessardCentre ÉCOBES-Recherche Et Transfert, Cégep de Jonquière, Quebec, Canada.
Elise DuchesneGroupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada.
Luc J HébertGroupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada.
Bernard BraisMontreal Neurological Institute and Hospital, McGill University, Quebec, Canada.
Xavier RodrigueCentre Interdisciplinaire de Recherche en Réadaptation Et Intégration Sociale (CIRRIS), Institut de Réadaptation en Déficience Physique de Québec, Quebec, Canada.
François RouthierÉcole Des Sciences de La Réadaptation, Faculté de Médecine, Université Laval, Quebec, Canada.
Krista BestÉcole Des Sciences de La Réadaptation, Faculté de Médecine, Université Laval, Quebec, Canada.
Jean-Denis BrissonGroupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada.
Florentin ThullierDépartement d'informatique Et de Mathématique, Université du Québec À Chicoutimi, Quebec, Canada.
Sébastien GabouryDépartement d'informatique Et de Mathématique, Université du Québec À Chicoutimi, Quebec, Canada.
Isabelle CôtéGroupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada.
Cynthia GagnonGroupe de Recherche Interdisciplinaire Sur Les Maladies Neuromusculaires (GRIMN), Centre intégré universitaire de santé et de services sociaux du Saguenay-Lac-St-Jean, 2230 de L'Hôpital, Cp 1200, Jonquière, Quebec, G7X 7X2, Canada. Cynthia.gagnon4@usherbrooke.ca.

Funding

CIHR PJT 159777
6 · The paper itself

Abstract

Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is among the most prevalent types of recessive ataxia worldwide. Given the accelerated therapeutic advances for many ataxias, there is a need to improve trial readiness. This study aimed to document the progression of balance, lower limb coordination and mobility in adults with ARSACS according to their mobility stage (walker or not) over the trial-relevant time frame of two years, and responsiveness to change of related clinical outcome assessments (COAs). Sixty participants from two neuromuscular clinics (Saguenay and Québec City, Canada) were included. The COAs were the Lower Extremity Motor Coordination Test (LEMOCOT), Co-contraction index, 30-s Chair Stand test (30 s-CST), Timed Up & Go test (TUG), 10-Meter Walk Test (10mWT), Berg Balance Scale (BBS), and Activities-specific Balance Confidence-simplified (ABC-S) scale. Responsiveness was documented using an anchor-based method with self-perception of the progression of related COA outcomes in the previous year. A significant progression above the standard error of measurement was observed for the TUG (+ 7.8 s [24% compared with baseline]), 10mWT (-0.111 to-0.165 m/s [-17 to -20%]), BBS (-4.3 points [-24%]), and ABC-S (-4.3 points [-15%]), with some differences between mobility stages; participants using a walking aid or wheelchair showed greater progression. The TUG, 10mWT, and BBS were the most sensitive to change in COAs, detecting changes specifically in participants who reported getting worse. These results are pivotal for defining inclusion criteria and selecting COAs for future clinical trials.

Indexed as

Lower ExtremityMuscle SpasticityOutcome Assessment, Health CarePostural BalancePsychomotor PerformanceSpinocerebellar AtaxiasAdultDisease ProgressionFemaleHumansMaleMiddle AgedYoung AdultARSACSBalanceLower limb coordinationMobilityResponsiveness to change

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.