ORACLE: Efficacy of a Combined Linguistic/Communication Therapy in Acute Aphasia After Stroke

Sponsor
University Hospital, Toulouse (Other)
Overall Status
Recruiting
CT.gov ID
NCT03287544
Collaborator
(none)
18
1
2
57
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Study Details

Study Description

Brief Summary

Linguistic training is traditionally the gold standard for rehabilitation of aphasia after stroke and efficacy criteria count early stage, intensity as well as personalized treatment. To date, no clear evidence showed a specific effect of any therapy in the acute phase of aphasia after stroke. This study aims to compare the effect of a combined therapy (linguistic/communication) versus a linguistic therapy on communication performance in patients in the acute phase of aphasia after a first stroke.

Condition or Disease Intervention/Treatment Phase
  • Other: Combined rehabilitation
  • Other: Linguistic rehabilitation
N/A

Detailed Description

Twenty to 25% of strokes cause aphasia. Speech and language therapy is the well-known standard treatment of aphasia after stroke although it is based on weak scientific evidence. To date, the efficacy criteria of aphasia rehabilitation are early stage, intensity as well as personalized treatment. Usually these patients receive in acute phase a linguistic training focused on the linguistic impairment. This approach is based on the cerebral plasticity postulate. However the superiority of this practice compared to other methods has never been shown. Moreover the benefit of the combination gathering linguistic treatment with communication treatment has to our knowledge never been studied.

In the present study investigators propose to compare the effect of a combined linguistic/communication rehabilitation versus a linguistic treatment. To do so, investigators will recruit patients with aphasia after a first stroke, in the acute phase. After a allocation to the " combined " and " linguistic " groups, all the patients will have a comprehensive language and neuropsychological assessment before and after 3 months of rehabilitation, and finally 6 months after the onset.

The "linguistic" group will have a rehabilitation only focused on linguistic processes whereas the "combined" group will have a linguistic training as well as communication training. The therapy will be personalized and the therapists will exclusively use standardized linguistic and/or communication toolboxes of rehabilitation containing dedicated activities.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
18 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
There are two arms in the protocol: one experimental arm corresponding to the "combined" rehabilitation (linguistic/communication) compared with another arm corresponding to the "linguistic" rehabilitation. All included patients, after allocation based on aphasia severity to the " combined " and " linguistic " groups, will have a first evaluation (E1: language, neurologic and neuropsychological exams) within 7 days after the onset. Then after a 3 months rehabilitation period they will be assessed (E2: language, neurologic and neuropsychological exams). At 6 months after the onset they will finally have the last assessment (E3: language, neurologic and neuropsychological exams).There are two arms in the protocol: one experimental arm corresponding to the "combined" rehabilitation (linguistic/communication) compared with another arm corresponding to the "linguistic" rehabilitation. All included patients, after allocation based on aphasia severity to the " combined " and " linguistic " groups, will have a first evaluation (E1: language, neurologic and neuropsychological exams) within 7 days after the onset. Then after a 3 months rehabilitation period they will be assessed (E2: language, neurologic and neuropsychological exams). At 6 months after the onset they will finally have the last assessment (E3: language, neurologic and neuropsychological exams).
Masking:
Single (Outcomes Assessor)
Masking Description:
After the allocation in the groups, rehabilitation is not done blindly since the speech therapist knows what activities he offers to patients. However, the evaluations carried out by a speech therapist, are done without the knowledge of the rehabilitation group.
Primary Purpose:
Supportive Care
Official Title:
Effect of a Combined Language Therapy (Linguistic/Communication) on Aphasia After Stroke in Acute Phase: A Prospective, Controlled, Monocentric Pilot Study
Actual Study Start Date :
Mar 1, 2018
Actual Primary Completion Date :
Jun 30, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Combined rehabilitation

Linguistic training as well as communication training.

Other: Combined rehabilitation
Linguistic training as well as communication training.

Active Comparator: Linguistic rehabilitation

Rehabilitation only focused on linguistic processes.

Other: Linguistic rehabilitation
Rehabilitation only focused on linguistic processes.

Outcome Measures

Primary Outcome Measures

  1. Assessment of the communication performance. [Month 3]

    Assessed by the Lillois communication test

Secondary Outcome Measures

  1. Assessment of the communication performance. [Month 6]

    Assessed by the Lillois communication test

  2. Assessment of the linguistic performance. [Month 3; Month 6]

    Assessed by the "Score at understanding task".

  3. Assessment of the quality of life. [Month 3; Month 6]

    Assessed by the "Score at a specific quality of life scale ".

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • First stroke

  • Inclusion at the acute phase (< 7 days)

  • Patient registered at the social security system

  • French as usual language

  • Aphasia severity score measured by the Boston Diagnostic Aphasia Examination (BDAE) scale ≥ 1 and ≤ 4

  • Consent signed by the patient or if not, by the caregiver

Exclusion Criteria:
  • Cognitive impairment before the onset (IQCode > 3.4)

  • Alcohol or drug addiction

  • Untreated psychiatric disease,

  • Uncorrected sensory impairment

  • Evolutive pathology

  • Adults protected by Law

  • Participation to another research

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hôpital Pierre Paul Riquet Toulouse Midi-Pyrénées France 31059

Sponsors and Collaborators

  • University Hospital, Toulouse

Investigators

  • Principal Investigator: Lola Danet, Phd, University Hospital, Toulouse

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Toulouse
ClinicalTrials.gov Identifier:
NCT03287544
Other Study ID Numbers:
  • RC31/16/0018
  • 2017-A02163-50
First Posted:
Sep 19, 2017
Last Update Posted:
Aug 18, 2022
Last Verified:
Aug 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by University Hospital, Toulouse
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 18, 2022