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StrokeATNCT02768922

Aphasia Telerehabilitation

A study testing Aphasia telerehabilitation and Standard face-to-face aphasia rehabilitation in people with Stroke and Aphasia, run by Sunnaas Rehabilitation Hospital at 1 site in Norway.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This study aims at contributing with scientific evidence to the field of aphasia telerehabilitation. In Norway today, there is an unmet need for language training in post stroke aphasia and not all patients are offered language training. Read more about this study

Who is it for?
Ages 16 years and older
Conditions the study is for
Stroke, Aphasia
What is being tested?
Aphasia telerehabilitation and Standard face-to-face aphasia rehabilitation
Could I receive a placebo?
No, everyone receives an active treatment
How many people
62 participants
Where
1 siteNorway
Study dates
3 May 2016to 31 Dec 2018
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 16 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Patients with aphasia following stroke (all stages of aphasia post stroke)
  • Aphasia including naming impairment (percentile score of 70 or lower on the NGA - subtest naming)

Who cannot join

  • Age: < 16 years
  • Patients who are unable to perform 5 hours of speech and language therapy per week due to medical or cognitive reasons (Including vision and hearing impairment)

Trial locations and contacts

1 site in 1 country.

Norway1 site
  • Sunnaas Rehabilitation Hospital

    Nesoddtangen, 1453

Other trials in Norway

About this study

Official title: Aphasia Telerehabilitation Post Stroke

This study aims at contributing with scientific evidence to the field of aphasia telerehabilitation. In Norway today, there is an unmet need for language training in post stroke aphasia and not all patients are offered language training. Early start of aphasia rehabilitation and satisfying intensity do not seem to be standard clinical practice. Language training by telemedicine could improve this situation, and this study seeks to answer the question whether aphasia rehabilitation delivered by videoconference can improve language function in aphasia post stroke.

Read the detailed description

BACKGROUND:

About 25 % of all stroke cases lead to aphasia. Aphasia can include difficulties with speech production and comprehension, as well as reading and writing impairment. Language impairment affects post stroke rehabilitation in a negative manner. Quality of life is reduced in persons with aphasia compared to stroke victims without aphasia. Speech and language therapy is the main form of aphasia rehabilitation. The most updated Cochrane review indicates that intensive speech and language therapy is more effective than therapy of lower intensity. Current aphasia services in Norway do not seem to be in accordance with the national guidelines for treatment and rehabilitation of stroke. The capacity for aphasia rehabilitation at the community level is too small and there is a lack of speech -language pathologists (SLPs). Language training by videoconference could improve this unmet need for language training in post stroke aphasia. The literature within this field is however sparse and there is a substantial lack of studies showing the effectiveness of telerehabilitation. Financed by the Norwegian Foundation for Health and Rehabilitation, the investigators have earlier performed a feasibility study at Sunnaas Rehabilitation Hospital in cooperation with the Norwegian Centre for Integrated Care and Telemedicine. This feasibility study showed that language training by videoconference is feasible with regard to technical, practical and rehabilitation aspects. The feasibility study laid ground for a larger and controlled study.

OBJECTIVE:

The project aims at contributing with scientific evidence to the field of aphasia telerehabilitation. The objective of this randomized controlled clinical trial is to investigate the feasibility and effectiveness of speech and language training given by videoconference.

DESIGN:

The study will be conducted as a pragmatic exploratory randomized controlled clinical trial (RCT) with an intervention and a control group. The patients will be assessed at inclusion and before randomization (baseline), and at 4 weeks and 4 months post randomization. Testing is blinded.

PARTICIPANTS:

Patients will be recruited from the stroke units at Oslo University Hospital, Akershus University Hospital, Østfold Hospital,and Bærum Hospital. Patients, who are admitted for rehabilitation at Sunnaas Rehabilitation Hospital, will also be included. In addition, patients earlier treated or on the waiting list at Sunnaas Rehabilitation Hospital, will be invited to participate. The investigators will also try to recruit patients from other rehabilitation institutions, and in cooperation with SLPs in the region of Oslo, Østfold and Akershus. The investigators will also invite for participation through the Aphasia Association of Norway (user organization).

The study aims at including 40 participants in each group, with a total number of 80 subjects. The investigators will include patients with aphasia in all stages following stroke including naming impairment. Patients under the age of 16 years and patients, who are unable to perform five hours of speech and language therapy per week due to medical or cognitive reasons, will be excluded.

INTERVENTION:

The intervention group will receive speech and language therapy via videoconference while the control group will not receive any specific therapy as part of this study. Both groups will receive standard aphasia rehabilitation (usual care). The amount of standard aphasia rehabilitation (usual care) will be logged in all participants. Participants in the intervention group will receive speech-language training (SLT) for five hours a week over four consecutive weeks. The SLT will be performed by an SLP using videoconference via internet from Sunnaas Rehabilitation Hospital to the laptop in the patient's home, or rehabilitation/nursing ward. To secure treatment fidelity and replication for future studies, the investigators have used the template for intervention description and replication (TiDieR) checklist and guide to describe the intervention. The investigators will use the technical solution "Cisco Jabber Video/Acano" and the remote control software "LogMeIn", in the telerehabilitation that is given.

PROCEDURES:

The stroke units will inform potential participants about the project and refer them to Sunnaas Rehabilitation Hospital for further investigation. Potential participants, who are patients at Sunnaas Rehabilitation Hospital, receive information about the project and an invitation to take part in the trial. For recruitment from other rehabilitation institutions, local speech and language therapists, and for members of the Aphasia association of Norway, advertising in form of a flyer and a brochure is used. After referral an ambulatory visit by the PhD-fellow or research SLP will be performed. Detailed information about the project will be provided and the research investigator will request an informed consent before carrying out baseline testing. Baseline assessment is blinded as it is performed before group allocation. The four weeks control and follow-up-testing is performed by external SLPs blinded to group allocation. Directly after the intervention period (four weeks), the participant will be visited at home or come to the outpatient clinic at Sunnaas Rehabilitation Hospital. The laptop will be retrieved and assessment performed. The control group will be tested at the corresponding time point. A further follow-up assessment will be performed four months post randomization in all participants. The four weeks control and follow-up-testing is performed by external SLPs blinded to group allocation.

OUTCOME MEASURES:

To investigate the effect of aphasia rehabilitation delivered by telemedicine, the investigators have chosen to look especially on naming as a measure of expressive language function. The investigators want to regard the prolonged effect of aphasia telerehabilitation on language function. Further on the investigators want to see the effect immediately after intervention and on other language functions than naming. The investigators also want to investigate whether SLT by videoconference can affect quality of life, if it is feasible and how persons with aphasia and therapists experience the telerehabilitation.

For the assessment of language functioning, the Norwegian Basic Aphasia Assessment (NGA) with the subtests conversational interview, naming, repetition and comprehension will be used.To assess the ability of sentence production, the investigators will use the Verb and Sentence Test (VAST) subtest sentence production. Functional communication will be assessed using Communicative Effectiveness Index (CETI). Quality of life will be assessed using Stroke and Aphasia Quality of Life scale (SAQOL-39). In addition, the experiences of patients, relatives and therapists with the telerehabilitation services will be assessed using a questionnaire as well as semi-structured interviews with selected patients. There will be an interview with the SLPs performing the telerehabilitation.

Primary endpoint: Naming ability four months post randomization.

Secondary endpoints:

  • Language functions other than naming (repetition, comprehension, sentence production) four months post randomization.
  • Functional communication and quality of life four months post randomization..
  • Naming and other language functions immediately after intervention.
  • How the telerehabilitation is experienced by patients and SLPs.
  • Feasibility of telerehabilitation with regards to ethical, technical, logistic, patient and data safety aspects.

ANALYSES AND STATISTICS:

The investigators will use an intention to-treat (ITT) analysis. The trial is a longitudinal study that will give continuous repeated measurements, and the data will be analyzed using Mixed-models. Data will be examined for differences over time and between groups. Subgroup analysis will be performed to explore factors considered to affect the outcome of the trial like differences in time since onset of stroke or demographic and stroke-related factors. Qualitative data collected from semi-structured interviews will be suitably coded.

Conditions
Stroke, Aphasia
Being tested
Aphasia telerehabilitation, Standard face-to-face aphasia rehabilitation
Keywords
Telemedicine, Telerehabilitation, Speech and language therapy
Medical subject headings
Stroke, Aphasia, Communication Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Aphasia telerehabilitationOther

    Speech and language therapy delivered by speech-language pathologist via computer and telemedicine

  • Standard face-to-face aphasia rehabilitationOther

    Speech and language therapy delivered by speech-language pathologist face-to-face (treatment as usual)

Study groups in NCT02768922
Study groupRoleWhat they receive
Aphasia telerehabilitationExperimentalSpeech and language therapy is given by telemedicine to improve expressive language function. The therapy will include knowledge based tasks of aphasia rehabilitation including training of language forms and overall functional communication. A special emphasis will be put on naming training. The telerehabilitation will be given in a addition to standard face-to-face aphasia rehabilitation
Receives: Other: Aphasia telerehabilitation; Other: Standard face-to-face aphasia rehabilitation
ControlActive comparatorControl Group receives standard face-to-face aphasia rehabilitation
Receives: Other: Standard face-to-face aphasia rehabilitation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Naming ability assessed by NGA

    Will be assessed by the Norwegian Basic Aphasia Assessment (NGA) subtest "naming"

    Measured: four month post randomization

Secondary outcomes (12)
  1. Language function other than naming (repetition) assessed by NGA

    Repetition will be assessment by the Norwegian Basic Aphasia Assessment (NGA) subtest "repetition".

    Measured: four month post randomization

  2. Language function other than naming (comprehension ) assessed by NGA

    Comprehension will be assessment by the Norwegian Basic Aphasia Assessment (NGA) subtest "comprehension".

    Measured: four month post randomization

  3. Sentence Production by VAST

    Sentence production will be assessed by the Verb and sentence test (VAST)

    Measured: four month post randomization

  4. Sentence Production by VAST

    Sentence production will be assessed by the Verb and sentence test (VAST)

    Measured: immediately after intervention (4 weeks)

  5. Functional communication assessed by CETI

    Functional communication will be assessed using Communicative Effectiveness Index (CETI).

    Measured: four month post randomization

  6. Naming immediately after intervention assessed by NGA

    Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "naming"

    Measured: immediately after intervention (4 weeks)

  7. Repetition immediately after intervention assessed by NGA

    Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "repetition"

    Measured: immediately after intervention (4 weeks)

  8. Comprehension immediately after intervention assessed by NGA

    Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "comprehension"

    Measured: immediately after intervention (4 weeks)

  9. Experiences of patients with the telerehabilitation by questionnaire

    Will be assessed by a questionnaire

    Measured: four month post randomization

  10. Experiences of patients with the telerehabilitation by semi-structured interviews.

    Will be assessed by semi-structured interviews with selected patients

    Measured: through study completion, an average of 2 year

  11. Experiences of SLPs with the telerehabilitation by semi-structured interviews

    Will be assessed by semi-structured interviews with selected patients

    Measured: through study completion, an average of 2 year

  12. Quality of life assessed by SAQOL-39.

    Quality of life will be assessed using Stroke and Aphasia Quality of Life scale (SAQOL-39).

    Measured: four month post randomization

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 May 2016 (estimated)
  2. Study start3 May 2016
  3. Primary completion27 Sep 2018
  4. Study completion31 Dec 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
62 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02768922
Sponsor's protocol ID
21524505
Acronym
AT
Status last verified
Mar 2019
First submitted
25 Apr 2016
Last updated
1 Apr 2019
Results posted
No
Data monitoring committee
Yes
Individual data sharing
Yes: The project will result in a Doctor of Philosophy (PhD) -thesis based on articles in international peer-reviewed scientific journals. In addition, the results of the project will be disseminated through national and international conference contributions as well as Norwegian publications in scientific journals, journals of user organizations and media contributions.

Publications

  • Ora HP, Kirmess M, Brady MC, Sorli H, Becker F. Technical Features, Feasibility, and Acceptability of Augmented Telerehabilitation in Post-stroke Aphasia-Experiences From a Randomized Controlled Trial. Front Neurol. 2020 Jul 31;11:671. doi: 10.3389/fneur.2020.00671. eCollection 2020.

    PubMed 32849176
  • Ora HP, Kirmess M, Brady MC, Winsnes IE, Hansen SM, Becker F. Telerehabilitation for aphasia - protocol of a pragmatic, exploratory, pilot randomized controlled trial. Trials. 2018 Apr 2;19(1):208. doi: 10.1186/s13063-018-2588-5.

    PubMed 29606148

Questions about this trial

What is this clinical trial studying?

A study testing Aphasia telerehabilitation and Standard face-to-face aphasia rehabilitation in people with Stroke and Aphasia, run by Sunnaas Rehabilitation Hospital at 1 site in Norway.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Apr 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Naming ability assessed by NGA (time frame: four month post randomization). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02768922, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Apr 2019.

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Aphasia Telerehabilitation (NCT02768922) | AzTrials