ClinicalTrials.gg
CompletedNCT04566081Updated Mar 10, 2026Results posted

Digital Interventions in Neurorehabilitation: iTALKbetter

An interventional study of iTalkBetter Trained Items and iTalkBetter Untrained Items in Stroke, Aphasia and Anomia, sponsored by University College, London. Completed at 1 site in United Kingdom. Per ClinicalTrials.gov, last updated 2026-03-10.

Sponsored by University College, London · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Not applicable
Sex
All
01

Study summary

iTALKBetter will provide an app-based therapy for people with word retrieval difficulties who have had a stroke.

This study aims to test the therapy application for people with naming difficulties through a small scale item-randomized controlled trial.

Read the detailed description

Mortality from stroke in the UK has reduced from 21% in 1999 to 12% in 2008. However, stroke prevalence has been increasing, the consequence of socioeconomic and scientific advances that have improved survival; which means that more people are surviving with long-standing disability. Language impairment (aphasia) is the second most common major impairment after stroke, with a prevalence of 250,000 in the UK. Aphasia may respond to therapy many months and years after the stroke occurs, but provision of specialist therapy (speech and language therapy - SALT) is far below that needed to provide optimal rehabilitation.

The investigators will address this by targeting a common symptom of post-stroke aphasia: impaired word retrieval problems. This is particularly important in patients receiving rehabilitation for associated disabilities as poor speech production can impair participation/compliance with treatment programmes. The study is designed to improve word retrieval in patients with post-stroke aphasia, who are in the chronic phase (>6 months post-stroke).

The main aim is to test the clinical efficacy of a novel, web-based, DNI. iTALKbetter will provide an effective training tool that patients can use to practice independently. This will free-up SALT time to provide additional assessment, supervision and functional intervention in a highly cost effective manner.

iTALKbetter will provide an app-based therapy for people with word retrieval difficulties who have had a stroke (naming app for a wide variety of common words and phrases).

This Digital Neuro Intervention (DNI) will provide the opportunity for the necessary increased rehabilitation to help people recover lost naming function. This will alleviate NHS Speech and Language Therapist (SALT) time and put users in control of when and where they carry out practice-based language therapy.

Purpose iTALKbetter will provide an app-based therapy for people with word retrieval difficulties who have had a stroke (naming app for a wide variety of common words and phrases).

What does it do? The DNI works via mass practice and feedback to the users on a trial-by-trial basis. The DNI is very simple in a way; it just presents a long series of pictures for users to name. The DNI will use speech recognition (SR) software in order to make a binary decision as to whether the user said the correct word or not. This affects what the next trial (object to name) is and what auditory cue (if any) is provided the next time the user has to name the same item.

What is the clinical trial design? A small, well-defined sample of patients with the potential to benefit from the DNI will be recruited. The main outcome measure is whether the DNI is effective at improving naming impairments on trained vs. untrained items. This comparison is within-subject and is achieved by comparing post-therapy measures to multiple baseline measures.

Outcome measures will be collected by the research team using a variety of standardized and non-standardized tests of language and cognition. These outcome measures are not built into the DNI at this point.

The DNI will be introduced to the participant when attending a testing session. One of the research team will explain how to use the DNI, provide instructions for the user, and give some time for practice items. When confident that the participant can use the DNI independently, the participant will take the device home and continue their therapy (suggested therapy time is 5-10 hours per week) which will be simultaneously monitored by the research team. The research team will also check in on the participant weekly to trouble shoot any difficulties they may have (whether motivational or technical). When the participant has completed the therapy block, they will be invited in again for testing and they will return the mobile device with the DNI on it. The participants who continue to receive standard care during the therapy block will be asked to record and submit details to the research team

Why is the research considered worth doing? Standard (face to face) Speech and Language Therapy (SALT) has a huge evidence-base but patients in the NHS have unmet therapy needs due to a lack of resources. The evidence from speech-therapy highlights the amount of time-on-task required to improve patients' ability to communicate. Naming problems are common and impact on the patients' wellbeing and social inclusion. There is also good evidence that current existing therapeutic approaches work.

A Cochrane review of 39 RCT's involving 2518 participants concluded that speech-therapy results in significant benefits to patients' functional communication. Many of these studies involve high doses of therapy. A meta-analysis examining dose found that positive therapy studies averaged 98 hours of speech therapy in total, while negative studies averaged 43. In the NHS a patient with aphasia can expect a total average of 6-10 hours of SALT. When the intervention takes place or how intensely seems less relevant to recovery. The solution to the lack of available SALT therapy is to produce digital neuro-interventions that give patients the opportunity to practice scientifically validated, impairment based therapy when and where it suits them which gives them access to optimum therapy dose.

Recent improvements in acute stroke care means that demand for already limited NHS resources will increase. Commissioners will need to address this growing unmet need and innovative relatively cheap interventions like this one will provide necessary rehabilitation.

Therapy can be effortful for patients who can sometimes be too fatigued when the therapist comes to do their session. This digital neuro-intervention will provide optimum availability of therapy and therefore place the patient in control of how much they do. The investigators aim to combat this by creating an engaging and adaptive therapy. The adaptiveness will serve to reward the patients for their efforts without ever making them feel like they are failing. This will hopefully boost how long they spend in therapy and therefore make greater gains.

There are therapy 'apps" available for patients with aphasia but the scientific basis for them is lacking and none are targeted for speech production. By using voice recognition software the intervention will be uniquely designed to be used by patients with word retrieval impairments.

What new information will the research provide? The concept of the therapy component is based on standard SALT practice and thus has a strong proof of concept basis, as do the proposed outcome measures. The novel component is packaging it in a user- friendly web-app that is designed for and by people with word-retrieval problems. This is ambitious and yet realistic goal to provide a world-wide evidence-based therapy that can benefit many. This digital neuro-intervention will be in contrast to the plethora of apps available online claiming cognitive training without having scientific proof.

The iTALKbetter research study is a small-scale, randomised, clinical trial for participants with word retrieval impairments post-stroke. The main research question is whether iTALKbetter improves patients' naming ability for trained items. This hypothesis is tested by assessing participants naming abilities on two matched lists of items, half are trained items and half are untrained.

Participants practice with the therapy for set periods of time (therapy block) following a series of (three) baseline measures split over a single, pre-therapy block. The main outcome measure will be a clinically relevant improvement on the naming ability of the trained items (compared to untrained control items).

The investigators also plan to capture brain-based data (structural MRI) in order to test a series of secondary hypotheses relating to both how and why the therapy may work in some participants but not others. All brain imaging will be outside of standard care for the participants and take place at UCL by trained staff.

Hypotheses and Objectives H1-Primary: Does iTB improve naming performance on trained items?

This is a within-subject comparison. The criteria for success is a 10% (raw, or unstandardized) relative improvement in performance. This effect size was used in the recent Big Cactus study.

Primary Objective: Does iTB improve naming performance on trained items?

Secondary Objective(s):

The investigators believe that using this DNI will improve word retrieval on trained items by providing a known therapy used by SLT's through a digital app and by enabling an increased dose of therapy. However, another objective is that by using this DNI and practicing every day, there will be changes in participants' brain structure and in the health of the participants and their carers.

  • Are the therapy effects item-specific or do is there generalization to untrained items?
  • Are the effects of the DNI therapy limited to the language domain alone or do they improve in other cognitive domains (e.g. sustained attention)?
  • Does the DNI improve participant's social activity and participation?
  • Is the DNI acceptable to participants (can they use it easily)?
  • Is the DNI acceptable to participants' carers?
  • Does the DNI improve carer health/well-being?
  • Does the DNI have any economic benefits?
  • Can baseline structural brain imaging explain participants' responses to the DNI?
  • Can baseline structural brain imaging be used to predict incoming participants' response to the DNI?
  • Can repeated-measures structural brain imaging identify participants' brain areas that change in response to the DNI?
02

Conditions studied

  • Stroke
  • Aphasia
  • Anomia

Keywords

  • Anomia
  • Word Retrieval
  • Digital Therapy
03

In context

Stroke

8,255 studies on the registry are indexed under Stroke; 2,056 are open to participants now.

This study's enrollment of 31 is below the median of 49 across 6,024 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

University College, London is the lead sponsor of 651 studies on the registry; 149 are open to participants now.

Of its 6 completed or terminated interventional studies of FDA-regulated products, 2 (33%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Any type of stroke but at least 6 months after onset.
  • Evidence of aphasia on the Comprehensive Aphasia Test
  • English as their dominant language
  • Able to tolerate MRI brain scan
  • Able to give
  • Able to use the DNI (app)

Exclusion criteria

Exclusion Criteria:

  • No diagnosis of developmental language disorders
  • No diagnosis of severe dementia or primary progressive aphasia
  • No major co-existing neurological or psychiatric diagnosis
  • No to brain scanner (e.g. the presence of ferromagnetic implants or other metallic or electronic objects in the body, weight over 24 stone, claustrophobia or pregnancy).
Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Contraindication

A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
31 participants (actual)

Study arms

  • Experimental
    iTALKbetter

    There is only one arm (iTalkBetter), but within this arm there are two conditions, trained and untrained items. These are the therapy items (words). Half are trained and half are untrained. Each participant gets a different mix of trained or untrained items. Participants received iTALKbetter therapy for 6 weeks. Participants are required to use the therapy for 1.5 hours everyday to reach the required dose of 60 hours over the 6 week period.

    Behavioral: iTalkBetter Trained Items · Behavioral: iTalkBetter Untrained Items

Interventions

  • BehavioraliTalkBetter Trained Items

    These are the linguistic items to-be-trained

  • BehavioraliTalkBetter Untrained Items

    These are the psycholinguistically matched untrained items

06

What researchers measure

Primary outcomes

  1. Accuracy Performance (%) on a Bespoke Word Retrieval Test: WRT. Two Conditions: 1. Trained Items 2. Untrained Items

    The WRT is custom test of word retrieval comprised of a subset of the trained and untrained items form the iTALKbetter therapy. Participants accuracy on the word retrieval test is measured at two timepoints: pre intervention (T3), and post intervention (T4). There are 110 trained and 110 untrained items. Accuracy is reported as a percentage score (min = 0%, max = 100%) for each of the four conditions. The outcome is the percentage change in performance on the WRT. To investigate the efficacy of iTalkBetter in improving the retrieval of trained single words on the WRT, a repeated measures ANOVA was used which compared change in accuracy over the pre-therapy block and the therapy block. There were two factors, each with two levels: time (pre-therapy (Baseline to T3) and therapy (T3 to T4)); and item (trained and untrained lexical items).

    Time frame: Two time points: 1. Pre- intervention (T3 = 6 weeks post baseline) 2. Post-intervention (T4 = 12 weeks post baseline)

Secondary outcomes

  1. Qualitative Interviews

    Semi-structured interviews were carried out with partcipants to better understand why they took part in the study, and what they hoped to gain (baseline) and then reflections on what it was like taking part in the study (Last time point)

    Time frame: Baseline and Post-intervention (T4 = 12 weeks post Baseline)

07

Results

Posted Mar 10, 2026

Participant flow

31 PWA were recruited for the study. Recruitment was from the Predicting Language Outcome and Recovery After Stroke (PLORAS) database and from a local outpatient clinic. Between Sep 7, 2020 and Mar 1, 2022.

Participant flow — Overall Study
MilestoneiTalkBetter Therapy Group
Started31
Completed27
Not completed4
Withdrew: Death1
Withdrew: Withdrawal by subject3

Outcome measures

PrimaryAccuracy Performance (%) on a Bespoke Word Retrieval Test: WRT. Two Conditions: 1. Trained Items 2. Untrained Items

The WRT is custom test of word retrieval comprised of a subset of the trained and untrained items form the iTALKbetter therapy. Participants accuracy on the word retrieval test is measured at two timepoints: pre intervention (T3), and post intervention (T4). There are 110 trained and 110 untrained items. Accuracy is reported as a percentage score (min = 0%, max = 100%) for each of the four conditions. The outcome is the percentage change in performance on the WRT. To investigate the efficacy of iTalkBetter in improving the retrieval of trained single words on the WRT, a repeated measures ANOVA was used which compared change in accuracy over the pre-therapy block and the therapy block. There were two factors, each with two levels: time (pre-therapy (Baseline to T3) and therapy (T3 to T4)); and item (trained and untrained lexical items).

Time frame:
Two time points: 1. Pre- intervention (T3 = 6 weeks post baseline) 2. Post-intervention (T4 = 12 weeks post baseline)
Reported as:
Mean · percentage
Accuracy Performance (%) on a Bespoke Word Retrieval Test: WRT. Two Conditions: 1. Trained Items 2. Untrained Items
percentageiTALKbetter
Trained items (T3)38.3 ± 0.85
Untrained items (T3)38.4 ± 0.95
Trained items (T4)50.6 ± 1.8
Untrained items (T4)43 ± 1.95
Statistical analysis
  • iTALKbetter · ANOVA · p = 0.003 · F value: 10.41
SecondaryQualitative Interviews

Semi-structured interviews were carried out with partcipants to better understand why they took part in the study, and what they hoped to gain (baseline) and then reflections on what it was like taking part in the study (Last time point)

Time frame:
Baseline and Post-intervention (T4 = 12 weeks post Baseline)

Results for this outcome have not been posted.

Adverse events

Collected over From T1 to T5 (~30 weeks). Non-serious events are listed at a 0% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
iTALKbetter1/31 (3.2%)0/31 (0%)0/31 (0%)

Baseline characteristics

Age, Continuous
Age, Continuous(Years)iTALKbetter
Mean62 ± 12
Sex: Female, Male
Sex: Female, Male(Participants)iTALKbetter
Female7
Male20
Race and Ethnicity Not Collected
Race and Ethnicity Not Collected(Participants)iTALKbetter
Word Retrieval Test (WRT)
Word Retrieval Test (WRT)(Percentage)iTALKbetter
Mean32 ± 15.77
08

Study locations

1 site
  • University College London
    London, WC1E6BT, United Kingdom
09

References and documents

Publications

  • Upton E, Doogan C, Fleming V, Leyton PQ, Barbera D, Zeidman P, Hope T, Latham W, Coley-Fisher H, Price C, Crinion J, Leff A. Efficacy of a gamified digital therapy for speech production in people with chronic aphasia (iTalkBetter): behavioural and imaging outcomes of a phase II item-randomised clinical trial. EClinicalMedicine. 2024 Feb 21;70:102483. doi: 10.1016/j.eclinm.2024.102483. eCollection 2024 Apr. PubMed 38685927 ↗

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Sep 2020 to primary completion in Feb 2022, 17 months.

Results were first posted in Mar 2026, 4 years after primary completion.

Of 3,108 non-industry interventional studies with no phase under Stroke, half reached primary completion within 23 months of starting (the median), counting those still running; a quarter within 10 and three quarters within 46. This study's 17 months is below that.

Counting every sponsor, half of 3,252 studies reached it within 23 months; a quarter within 10 and three quarters within 46.

How these figures are worked out, and which studies are left out of them.

Registered
May 29, 2020
First posted
Sep 28, 2020
StartActual
Sep 7, 2020
Primary completionActual
Feb 25, 2022
CompletionActual
Feb 25, 2022
Results first posted
Mar 10, 2026
Last update
Mar 10, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Mar 10, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT04566081
Responsible party
Sponsor
First posted
Sep 28, 2020
Start date
Sep 7, 2020
Primary completion
Feb 25, 2022
Completion
Feb 25, 2022
Results posted
Mar 10, 2026
Last update
Mar 10, 2026

Study contacts

Alexander P Leff, Professor
principal investigator · University College, London

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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