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.
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
- 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.
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.
- 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 group | Role | What they receive |
|---|---|---|
| Aphasia telerehabilitation | Experimental | Speech 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 |
| Control | Active comparator | Control 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.
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)
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
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
Sentence Production by VAST
Sentence production will be assessed by the Verb and sentence test (VAST)
Measured: four month post randomization
Sentence Production by VAST
Sentence production will be assessed by the Verb and sentence test (VAST)
Measured: immediately after intervention (4 weeks)
Functional communication assessed by CETI
Functional communication will be assessed using Communicative Effectiveness Index (CETI).
Measured: four month post randomization
Naming immediately after intervention assessed by NGA
Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "naming"
Measured: immediately after intervention (4 weeks)
Repetition immediately after intervention assessed by NGA
Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "repetition"
Measured: immediately after intervention (4 weeks)
Comprehension immediately after intervention assessed by NGA
Assessed by Norwegian Basic Aphasia Assessment (NGA) subtest "comprehension"
Measured: immediately after intervention (4 weeks)
Experiences of patients with the telerehabilitation by questionnaire
Will be assessed by a questionnaire
Measured: four month post randomization
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
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
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.
- First posted11 May 2016 (estimated)
- Study start3 May 2016
- Primary completion27 Sep 2018
- Study completion31 Dec 2018
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for StrokeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Sunnaas Rehabilitation Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- South-Eastern Norway Regional Health Authority
- Responsible party
- Principal investigator, Frank Becker, Sunnaas Rehabilitation Hospital
- Investigators
- Frank Becker, PhD, Study director, Sunnaas Rehabilitation Hospital
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 32849176Ora 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
Study at a glance
From the registry record, last updated by the sponsor on 1 Apr 2019. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Aphasia Telerehabilitation Post Stroke
- ClinicalTrials.gov ID
- NCT02768922
- Acronym / sponsor ID
- AT / 21524505
- Keywords
- Telemedicine, Telerehabilitation, Speech and language therapy
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 62 participants (actual)
- Lead sponsor
- Sunnaas Rehabilitation HospitalUniversity, hospital or other
- Collaborators
- South-Eastern Norway Regional Health Authority
- Study start
- 3 May 2016 (actual)
- Primary completion
- 27 Sep 2018 (actual)
- Study completion
- 31 Dec 2018 (actual)
- First posted
- 11 May 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Aphasia telerehabilitation | Experimental | Other: Aphasia telerehabilitation, Other: Standard face-to-face aphasia rehabilitationSpeech 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 |
| Control | Active comparator | Other: Standard face-to-face aphasia rehabilitationControl Group receives standard face-to-face aphasia rehabilitation |
Who may qualify
- Ages
- 16 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (2 listed)
- 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)
Key exclusion criteria (2 listed)
- 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)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Aphasia telerehabilitationSpeech and language therapy delivered by speech-language pathologist via computer and telemedicine | Other | Aphasia telerehabilitation |
| Standard face-to-face aphasia rehabilitationSpeech and language therapy delivered by speech-language pathologist face-to-face (treatment as usual) | Other | Aphasia telerehabilitation, Control |
Primary outcome
Naming ability assessed by NGA
Time frame: four month post randomization
Will be assessed by the Norwegian Basic Aphasia Assessment (NGA) subtest "naming"
12 secondary outcomes
Language function other than naming (repetition) assessed by NGA
Time frame: four month post randomization
Language function other than naming (comprehension ) assessed by NGA
Time frame: four month post randomization
Sentence Production by VAST
Time frame: four month post randomization
Sentence Production by VAST
Time frame: immediately after intervention (4 weeks)
Functional communication assessed by CETI
Time frame: four month post randomization
Naming immediately after intervention assessed by NGA
Time frame: immediately after intervention (4 weeks)
Repetition immediately after intervention assessed by NGA
Time frame: immediately after intervention (4 weeks)
Comprehension immediately after intervention assessed by NGA
Time frame: immediately after intervention (4 weeks)
Experiences of patients with the telerehabilitation by questionnaire
Time frame: four month post randomization
Experiences of patients with the telerehabilitation by semi-structured interviews.
Time frame: through study completion, an average of 2 year
Experiences of SLPs with the telerehabilitation by semi-structured interviews
Time frame: through study completion, an average of 2 year
Quality of life assessed by SAQOL-39.
Time frame: four month post randomization
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 Apr 2019.
- Derived from this study: PubMed 32849176Ora 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.
- Derived from this study: PubMed 29606148Ora 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.
- pdf-file of Norwegian publication presenting the pilot study that led to this RCTLink provided by the sponsor.
- pdf-file of full report from the pilot study (Norwegian)Link provided by the sponsor.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Frank Becker, PhD study director
Sunnaas Rehabilitation Hospital
1 site in 1 country: see every site and its status.
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.