Evidence map›Paper›PMID 38502672›Full record

ArticlePloS one2024

Feasibility and utility of in-home body weight support harness system use in young children treated for spinal muscular atrophy: A single-arm prospective cohort study.

Megan A Iammarino, Lindsay N Alfano, Natalie F Reash, Brenna Sabo, Sara Conroy, Garey Noritz, Madalynn Wendland, Linda P Lowes

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05715749 (Exploring the Feasibility and Utility of In-home Body Weight Support Harness System Use in Children Treated for Spinal Muscular Atrophy), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.9field-weighted citation impact, top 27% of its field
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.

NCT05715749 nacompletednot on this map

Exploring the Feasibility and Utility of In-home Body Weight Support Harness System Use in Children Treated for Spinal Muscular Atrophy: a Pilot Study

TypeinterventionalSponsorNationwide Children's HospitalRan2018 to 2024Enrolled33ConditionsSpinal Muscular Atrophy Type I, Spinal Muscular Atrophy Type IIArmsIn-home body weight support harness system
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

8 authors at 2 institutions in 1 country.

Megan A IammarinoCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, United States of America.ORCID 0000-0003-2800-3855
Lindsay N AlfanoCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, United States of America.
Natalie F ReashCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, United States of America.
Brenna SaboCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, United States of America.
Sara ConroyCenter for Biostatistics, The Ohio State University Wexner Medical Center, Columbus, Ohio, United States of America.
Garey NoritzDepartment of Pediatrics, Nationwide Children's Hospital, Columbus, Ohio, United States of America.ORCID 0000-0001-7308-3810
Madalynn WendlandDoctor of Physical Therapy Program, Cleveland State University, Cleveland, Ohio, United States of America.ORCID 0000-0003-3897-1315
Linda P LowesCenter for Gene Therapy, Nationwide Children's Hospital, Columbus, Ohio, United States of America.
Nationwide Children's Hospital · USCleveland State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis single-arm prospective cohort study aimed to evaluate the feasibility and utility of in-home body weight support harness system (BWSS) use in children treated for spinal muscular atrophy (SMA).

methodsIndividuals with 2 or 3 copies of SMN2 who received pharmacotherapeutic treatment, had head control, and weight <50lbs were enrolled. Families were provided a BWSS and documented use. Motor outcome assessments were completed at baseline, month 3 and month 6. Families provided feedback in an end of study survey.

resultsAll 32 participants (2.9 (SD 1.9) yrs), improved or remained stable on all outcomes. Average reported frequency of use was 4.1(2.3) hrs/week. Controlling for other covariates, frequency of use explained over 70% of the variability in change scores. Family feedback was overwhelmingly positive.

conclusionUse of in-home BWSS is a safe, feasible and useful option to increase exercise dosage after treatment in SMA and may help optimize motor abilities.

trial registrationStudy registered with: Clinicaltrials.gov Clinicaltrials.gov identifier: NCT05715749.

Indexed as

Muscular Atrophy, SpinalSpinal Muscular Atrophies of ChildhoodBody WeightChildChild, PreschoolExerciseFeasibility StudiesHumansProspective Studies

Identifiers

PMID38502672
PMCPMC10950233
OpenAlexW4392947913

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.