Evidence map›Paper›PMID 28748108›Full record

ArticlePilot and feasibility studies2018

ReaDySpeech for people with dysarthria after stroke: protocol for a feasibility randomised controlled trial.

Claire Mitchell, Audrey Bowen, Sarah Tyson, Paul Conroy

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Pilot and feasibility studies, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.3field-weighted citation impact, top 19% 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.

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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Stroke-associated dysarthria.Frontiers in neurology · 2025
    Review
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Claire MitchellDivision of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, University of Manchester MAHSC, Manchester, UK.ORCID 0000-0002-2445-8468
Audrey BowenDivision of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, University of Manchester MAHSC, Manchester, UK.
Sarah TysonDivision of Nursing, Midwifery & Social Work, University of Manchester, MAHSC, Manchester, UK.
Paul ConroyDivision of Neuroscience and Experimental Psychology, Faculty of Biology, Medicine and Health, University of Manchester MAHSC, Manchester, UK.
Manchester Academic Health Science Centre · GB

Funding

Department of Health DRF-2014-07-043
6 · The paper itself

Abstract

backgroundDysarthria, a disordered speech production resulting from neuro-muscular impairment, is a common symptom after stroke. It causes significant problems for patients' speech intelligibility, communication, psychological well-being, social engagement and stroke recovery. Rehabilitation for dysarthria is variable in quality, intensity and duration, which may be, in part, due to the lack of good quality evidence. An online therapy programme, ReaDySpeech, has the potential to improve quality, intensity and duration of speech rehabilitation and was considered in a proof-of-concept study to be acceptable to speech and language therapists and patients which warranted further evaluation. The present study aims to examine the feasibility of running a trial using the ReaDySpeech intervention. METHODS/

designA feasibility, randomised controlled trial, will recruit a minimum of 36 people with post-stroke dysarthria who are more than 1 week post stroke. Participants will be externally randomised in a 2:1 ratio to receive either ReaDySpeech and usual care (24 participants) or usual care only (12 participants). This study is single blind with the researcher carrying out the baseline and outcome measures while blinded to treatment allocation. The primary objective is to assess the feasibility of conducting a larger Phase III trial. The specific objectives are to determine the following: recruitment rate and reasons for non-recruitment; loss of participants to follow-up; acceptability of randomisation; adherence to the intervention; delivery of ReaDySpeech and content; acceptability of outcome measures; success of blinding strategies; defining 'usual' care; and the implications of the intervention for the patient/family/carer. DISCUSSION: This study will involve a regional, multi-centre, randomised controlled feasibility trial of a complex intervention in order to evaluate whether a Phase III randomised controlled trial is feasible.

trial registrationCurrent Controlled Trials, ISRCTN84996500.

Indexed as

DysarthriaFeasibilityRandomised controlled trialSpeech/language therapy (SLT)Stroke

Identifiers

PMID28748108
PMCPMC5520339
OpenAlexW2734007221

What OpenQuestion holds

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LicenceCC BY
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.