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DUbbing Language-therapy CINEma-based in Aphasia Post-Stroke

Primary Purpose

Aphasia, Post-Ictal

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Language and functional communication therapy
Sponsored by
Instituto de Investigación Hospital Universitario La Paz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Aphasia, Post-Ictal focused on measuring Rehabilitation, Word dubbing, Functional communication

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • nonfluent aphasia due to unilateral stroke in the left hemisphere without neuroimaging evidence of lesions in the right hemisphere.
  • the patient should have received a standard program of conventional speech therapy after stroke, remaining with aphasia with the following characteristics: severely restricted language, poor repetition (even for single words), not exceeding the 70th percentile in the Boston Diagnostic Aphasia Examination (BDAE) for repetition. Moderately preserved language comprehension: listening comprehension exceeding the 15th percentile of BDAE (average score obtained in three areas: word comprehension, commands and complex ideational material).
  • Signed informed consent.

Exclusion Criteria:

  • Any clinical condition (short life expectancy, coexisting disease) or other characteristics that precluded appropriate follow-up.
  • Participation in any therapeutic trial evaluating poststroke recovery.

Sites / Locations

  • La Paz University HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Group 1: first to receive therapy

Group 2: second to receive therapy

Arm Description

27 patients that will receive study specific speech therapy in the first 3 months since study inclusion. From months 3-6 they will be group 2 controls.

27 patients that will receive study specific speech therapy during months 3-6 since study inclusion. During the first 3 months of the study period, they will be group 1 controls.

Outcomes

Primary Outcome Measures

Communicative Activity Log (CAL) questionnaire
Questionnaire that evaluates quantity and quality of aphasic patient communication, with 18 different questions in each item. Each question belonging to these two items is answered as a 6 point scale, where 0 is the worst and 5 is the best score.
Boston Diagnostic Aphasia Examination (BDAE)
Neuropsycological battery that evaluates language skills based on perceptual modalities (auditory, visual, and gestural), processing functions (comprehension, analysis, problem-solving), and response modalities (writing, articulation, and manipulation). There are five subtests which include: conversational and expository speech, auditory comprehension, oral expression, reading, and writing. Its results can be used to classify patient's language profiles into one of the localization based classifications of aphasia, and it also provides a severity rating.

Secondary Outcome Measures

General Health Questionnaire (GQH-12)
The General Health Questionnaire (GHQ) is a psychometric screening tool to identify common psychiatric conditions. It comprises 12 questions, each one with a four point scale answer.
Stroke and aphasia Quality of Life Scale (SAQOL-39)
SAQOL-39 is an interview-administered self-report scale that comprises the 49 items of the SS-QOL (modified to be communicatively accessible to people with aphasia) and 4 additional items that measure speech comprehension, difficulties with decision-making and and impact of language problems on family and social life. Questions are answered with a five point scale.
Western Aphasia Battery Revised (WAB-R)
This neuropsycological test assesses linguistic and non-linguistic skills comprised of 8 subtest (32 short tasks). It identifies aphasia and classifies the type and severity of aphasia disorders.
Stroke Aphasic Depression Questionnaire (SADQ10)
This is a brief questionnaire with 10 items testing depression symptoms within the last week in aphasic patients. Each item scores in a four point scale.

Full Information

First Posted
February 20, 2020
Last Updated
November 22, 2021
Sponsor
Instituto de Investigación Hospital Universitario La Paz
Collaborators
Universidad Pontificia Comillas, Asociación Afasia Activa, La Caixa Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT04289493
Brief Title
DUbbing Language-therapy CINEma-based in Aphasia Post-Stroke
Official Title
DUbbing Language-therapy CINEma-based in Aphasia Post-Stroke (DULCINEA). A Feasibility Cross-over Pilot-trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
December 18, 2020 (Actual)
Primary Completion Date
February 2023 (Anticipated)
Study Completion Date
February 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Instituto de Investigación Hospital Universitario La Paz
Collaborators
Universidad Pontificia Comillas, Asociación Afasia Activa, La Caixa Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The DULCINEA study aims to develop and validate a new therapy that integrates essential language characteristics and functional communication by dubbing scenes from television series that represent daily situations. It will be a randomized, crossed over, interventional pilot study recruiting 54 patients with poststroke nonfluent aphasia. Patients will be treated individually in 40-minute sessions twice a week for 8 weeks. In each session, a speech therapist and an actor will select the clips with muted words or sentences that have been detected as functionally meaningful for each patient. Outcomes will be assessed as significant differences in two aphasia tests.
Detailed Description
The DULCINEA study aims to develop and validate a new therapy that integrates essential language characteristics and functional communication by dubbing scenes from TV series that represent daily situations. It will be a randomized, crossed over, interventional pilot study recruiting 54 patients with poststroke nonfluent aphasia from the departments of Neurology and Rehabilitation from La Paz University Hospital and also from the "Afasia Activa" association. After meeting all inclusion and none of the exclusion criteria and signing informed consent, patients will be randomised (1:1) in two different treatment groups. The first group will receive therapy within the first 3 months of their inclusion with a subsequent period of another 3 months without therapy (thus, serving as group 2 controls). Group 2 will initiate therapy after 3 months since their inclusion (serving as group 1 controls during the first 3 months). Therapy consists of 17 sessions performed in a eight week period (1 baseline session and 16 dubbing sessions), each lasting 40 minutes, in which the patient will be asked to dubb words or sentences previously selected and considered as functionally meaningful for them. These words will be chosen through an online survey performed by a representative group of aphasic patients and the study patients´own relatives in the baseline treatment session. Outcomes will be assessed as significant differences in two aphasia tests (CAL questionnaire and the BDAE).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Aphasia, Post-Ictal
Keywords
Rehabilitation, Word dubbing, Functional communication

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Two groups with 27 patients in each one. Group 1 starts therapy in the first 3 months since study inclusion and from months 3-6 is group 2 control. Group 2 starts language therapy from months 3-6, serving previously as group 1 control.
Masking
Outcomes Assessor
Masking Description
A psychologist blinded to the patient´s clinical characteristics and study groups performs the outcome questionnaires three times for each patient during the study period.
Allocation
Randomized
Enrollment
54 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1: first to receive therapy
Arm Type
Experimental
Arm Description
27 patients that will receive study specific speech therapy in the first 3 months since study inclusion. From months 3-6 they will be group 2 controls.
Arm Title
Group 2: second to receive therapy
Arm Type
Experimental
Arm Description
27 patients that will receive study specific speech therapy during months 3-6 since study inclusion. During the first 3 months of the study period, they will be group 1 controls.
Intervention Type
Other
Intervention Name(s)
Language and functional communication therapy
Intervention Description
17 therapy sessions in which the patients will be asked to dubb words or sentences from television series previously considered functionally meaningful for them.
Primary Outcome Measure Information:
Title
Communicative Activity Log (CAL) questionnaire
Description
Questionnaire that evaluates quantity and quality of aphasic patient communication, with 18 different questions in each item. Each question belonging to these two items is answered as a 6 point scale, where 0 is the worst and 5 is the best score.
Time Frame
Changes in score at six months
Title
Boston Diagnostic Aphasia Examination (BDAE)
Description
Neuropsycological battery that evaluates language skills based on perceptual modalities (auditory, visual, and gestural), processing functions (comprehension, analysis, problem-solving), and response modalities (writing, articulation, and manipulation). There are five subtests which include: conversational and expository speech, auditory comprehension, oral expression, reading, and writing. Its results can be used to classify patient's language profiles into one of the localization based classifications of aphasia, and it also provides a severity rating.
Time Frame
Changes in score at six months
Secondary Outcome Measure Information:
Title
General Health Questionnaire (GQH-12)
Description
The General Health Questionnaire (GHQ) is a psychometric screening tool to identify common psychiatric conditions. It comprises 12 questions, each one with a four point scale answer.
Time Frame
Changes in score at six months
Title
Stroke and aphasia Quality of Life Scale (SAQOL-39)
Description
SAQOL-39 is an interview-administered self-report scale that comprises the 49 items of the SS-QOL (modified to be communicatively accessible to people with aphasia) and 4 additional items that measure speech comprehension, difficulties with decision-making and and impact of language problems on family and social life. Questions are answered with a five point scale.
Time Frame
Changes in score at six months
Title
Western Aphasia Battery Revised (WAB-R)
Description
This neuropsycological test assesses linguistic and non-linguistic skills comprised of 8 subtest (32 short tasks). It identifies aphasia and classifies the type and severity of aphasia disorders.
Time Frame
Changes in score at six months
Title
Stroke Aphasic Depression Questionnaire (SADQ10)
Description
This is a brief questionnaire with 10 items testing depression symptoms within the last week in aphasic patients. Each item scores in a four point scale.
Time Frame
Changes in score at six months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: nonfluent aphasia due to unilateral stroke in the left hemisphere without neuroimaging evidence of lesions in the right hemisphere. the patient should have received a standard program of conventional speech therapy after stroke, remaining with aphasia with the following characteristics: severely restricted language, poor repetition (even for single words), not exceeding the 70th percentile in the Boston Diagnostic Aphasia Examination (BDAE) for repetition. Moderately preserved language comprehension: listening comprehension exceeding the 15th percentile of BDAE (average score obtained in three areas: word comprehension, commands and complex ideational material). Signed informed consent. Exclusion Criteria: Any clinical condition (short life expectancy, coexisting disease) or other characteristics that precluded appropriate follow-up. Participation in any therapeutic trial evaluating poststroke recovery.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Blanca Fuentes Gimeno
Phone
917277444
Ext
+34
Email
blanca.fuentes@salud.madrid.org
First Name & Middle Initial & Last Name or Official Title & Degree
Elena de Celis Ruiz
Phone
917277444
Ext
+34
Email
elena.decelis.ruiz@idipaz.es
Facility Information:
Facility Name
La Paz University Hospital
City
Madrid
ZIP/Postal Code
28046
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Blanca Fuentes Gimeno
Phone
917277444
Ext
+34
Email
blanca.fuentes@salud.madrid.org
First Name & Middle Initial & Last Name & Degree
Elena de Celis Ruiz
Phone
917277444
Ext
+34
Email
elena.decelis.ruiz@idipaz.es
First Name & Middle Initial & Last Name & Degree
Blanca Fuentes Gimeno
First Name & Middle Initial & Last Name & Degree
Lydia de la Fuente Gómez
First Name & Middle Initial & Last Name & Degree
Cristian Sempere Iborra
First Name & Middle Initial & Last Name & Degree
María Alonso de Leciñana
First Name & Middle Initial & Last Name & Degree
Elena de Celis Ruiz
First Name & Middle Initial & Last Name & Degree
Raquel Gutiérrez Zúñiga
First Name & Middle Initial & Last Name & Degree
José López Tàppero
First Name & Middle Initial & Last Name & Degree
Marta Martín Alonso
First Name & Middle Initial & Last Name & Degree
Silvia Pastor Yvorra
First Name & Middle Initial & Last Name & Degree
Ricardo Riguel Bobillo
First Name & Middle Initial & Last Name & Degree
Gerardo Ruiz Ares
First Name & Middle Initial & Last Name & Degree
Jorge Rodríguez Pardo
First Name & Middle Initial & Last Name & Degree
Paloma Blanco
First Name & Middle Initial & Last Name & Degree
Nereida Bueno

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34991688
Citation
Fuentes B, de la Fuente-Gomez L, Sempere-Iborra C, Delgado-Fernandez C, Tarifa-Rodriguez A, Alonso de Lecinana M, de Celis-Ruiz E, Gutierrez-Zuniga R, Lopez-Tappero J, Martin Alonso M, Pastor-Yborra S, Rigual R, Ruiz-Ares G, Rodriguez-Pardo J, Virues-Ortega J, Borobia AM, Blanco P, Bueno-Guerra N. DUbbing Language-therapy CINEma-based in Aphasia post-Stroke (DULCINEA): study protocol for a randomized crossover pilot trial. Trials. 2022 Jan 6;23(1):21. doi: 10.1186/s13063-021-05956-5.
Results Reference
derived

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DUbbing Language-therapy CINEma-based in Aphasia Post-Stroke

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