Evidence map›Paper›PMID 33957997›Full record

ArticlePilot and feasibility studies2021

Feasibility, safety and acceptability of select outcome measures in a physiotherapy study protocol for boys with haemophilia.

Nicola Thorpe, Phillip Harniess, Eleanor Main, Nicola Hubert, Sarah Rand, David Stephensen, Ri Liesner, Melanie Bladen

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Pilot and feasibility studies, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04076306 (What is the Feasibility, Acceptability and Sensitivity of the iSTEP Exercise Test in Boys With Haemophilia?), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT04076306 nacompletednot on this map

What is the Feasibility, Acceptability and Sensitivity of the iSTEP Exercise Test in Boys With Haemophilia?

TypeinterventionalSponsorGreat Ormond Street Hospital for Children NHS Foundation TrustRan2018 to 2018Enrolled43ConditionsHemophiliaArmsiSTEP exercise testing
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. 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 3 institutions in 1 country.

Nicola ThorpeGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK. nicola.thorpe@gosh.nhs.uk.ORCID http://orcid.org/0000-0002-1709-7756
Phillip HarniessGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Eleanor MainUCL Great Ormond Street Institute of Child Health, London, UK.
Nicola HubertGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Sarah RandUCL Great Ormond Street Institute of Child Health, London, UK.
David StephensenKent Haemophilia Centre, Kent and Canterbury Hospital, Canterbury, UK.
Ri LiesnerGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Melanie BladenGreat Ormond Street Hospital for Children NHS Foundation Trust, London, UK.
Great Ormond Street Hospital for Children NHS Foundation Trust · GBGreat Ormond Street Hospital · GBKent and Canterbury Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is a lack of functional performance measures for children and young people with haemophilia (CYPwH) with associated control data from typically developing boys (TDB). The literature advocates development of a core set of outcome measures for different chronic conditions. As medical treatment improves, CYPwH are experiencing better outcomes; therefore, more challenging measures are required to monitor physical performance. Such testing is not performed routinely, due to practical and safety concerns.

aimEvaluate the feasibility, safety and acceptability of select outcome measures as part of a study protocol testing CYPwH; including myometry, 10 metre incremental shuttle walk test (10-m ISWT), iSTEP (an incremental step test, with data from TDB), and 1 week of accelerometry-wear at home.

methodsSixty-six boys aged 6-15 years with mild, moderate or severe haemophilia A or B (including inhibitors) attending routine clinics at Great Ormond Street Hospital were approached to participate. Descriptive statistics and content analysis were used to assess outcomes of feasibility, safety and acceptability, which included recruitment/retention rates, protocol completion within routine appointment timeframes, performance testing without serious adverse events/reactions (SAE/SARs), and acceptability to CYPwH of high-level performance measures.

resultsOutcomes were met: 43 boys completed testing at clinic review (Jan-Nov 2018) within a 10-month timeframe, retention was 95% at completion of protocol and no SAE/SARs were reported throughout testing.

conclusionFeasibility, safety and acceptability of the study protocol have been established in this population. Both high-level performance tests, iSTEP and 10-m ISWT, were an acceptable addition to boys' routine clinic appointments and could be safe, acceptable choices of outcome measure as part of a core set of tests for CYPwH. Further investigation of the psychometric properties for the iSTEP is now justified, in order for it to be used as a standardised, validated, reliable outcome measure in clinical or research settings.

trial registrationRetrospectively registered on September 3, 2019, on ClinicalTrials.gov (ID: NCT04076306 ).

Indexed as

10-m ISWTChildrenFeasibilityHaemophiliaiSTEPMyometryOutcomes

Identifiers

PMID33957997
PMCPMC8099992
OpenAlexW3158099711

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.