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ReaDySpeech: clinical testing

ReaDySpeech for people with dysarthria after stroke: initial clinical testing prior to feasibility study

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN90031373
Enrollment
12
Registered
2015-02-05
Start date
2015-03-01
Completion date
Unknown
Last updated
2019-02-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Stroke

Interventions

This is an initial clinical testing of ReaDySpeech, a computer based programme to deliver speech therapy exercises to patients. Patients will be set up with a programme in ReaDySpeech to test it out f

Sponsors

University of Manchester
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria for clinicians: Clinicians will be recruited from 4 North West NHS sites that have already agreed to be involved in both the preliminary testing phase of the study and the future feasibility study. These clinicians will have a stroke caseload. Inclusion criteria for patient participants: 1. Patients with dysarthria as a result of stroke as diagnosed by a speech and language therapist 2. Patients more than 12 weeks post stroke with no upper limit post stroke 3. Patients who are willing to trial the computer based programme ReaDySpeech. 4. Participants will present with dysarthria, willing and able to undertake communication therapy (in clinicians' opinion) 5. Sufficient ability in English to participate in therapy without a translator 6. Medically stable 7. Able to give informed consent to participate

Exclusion criteria

Exclusion criteria: There is no clinician exclusion criteria. Patient participant exclusion criteria: 1. Patients with cognitive or language difficulties that will prevent them giving informed consent or using a computer 2. Patients with insufficient grasp of English

Design outcomes

Primary

MeasureTime frame
Structured and open questions following testing phase of the intervention. The questions intend to find out training needs for patients and clinicians as well as support needs for patients and clinician.

Secondary

MeasureTime frame
Adherence to the online programme. Measured by online history of interaction.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026