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Clinical Trials/NCT05520528
NCT05520528
Active, not recruiting
Not Applicable

Impact of Group Participation on Adults With Aphasia

University of Arkansas1 site in 1 country40 target enrollmentSeptember 6, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Aphasia, Acquired
Sponsor
University of Arkansas
Enrollment
40
Locations
1
Primary Endpoint
Reading Comprehension Battery for Aphasia-2 (RCBA-2; LaPointe & Horner, 1998) Scores
Status
Active, not recruiting
Last Updated
10 months ago

Overview

Brief Summary

The purpose of the study is to examine the impact of group participation on adults with aphasia. Participants will complete a standard pre-and post-assessment of language abilities (speech, comprehension, reading, and/or writing). Then participants will attend 90-minute weekly reading group sessions during an academic semester.

Detailed Description

The objective of this research is to determine if attendance in groups positively impacts language skills, activity/participation, and/or quality of life in persons with aphasia. This study will employ a university-clinic based outpatient group to administer language intervention. The specific aims of this study are to determine if group participation improves (1) life participation as measured by self-report questionnaires, (2) intervention-specific language skills as measured by treatment-related measures (e.g., reading comprehension and written expression), and (3) performance on non-treated language test scores as measured by a language assessment battery. Participants will complete 4-5 individual testing sessions (e.g., initial assessment and pre-/post-testing), 7-12 group sessions (90-minute weekly reading group session), and 7-12 independent sessions at home (e.g., completion of weekly reading assignments). The participants will read through a designated book incrementally across multiple weeks. The activities completed during the group sessions will focus on improving reading comprehension and written expression skills. Participants will read assigned passages at home and during the group sessions. Participants will complete a Copy and Recall Treatment (CART) worksheet independently to facilitate improvements in writing keywords related to the reading materials. CART involves copying target words and progresses to writing words from recall (Beeson, et al.). Participants will complete a reading comprehension worksheet and engage in discussion regarding the assigned book chapter. Reading comprehension and written expression data will be collected and analyzed to compare the pre-treatment baseline performance from the first treatment session to the post-treatment performance from the last treatment session. Pre-and post-testing scores will be analyzed to investigate the change in scores across the 2-time points to determine the relative effectiveness of book club participation for improving reading comprehension, written expression, and life participation.

Registry
clinicaltrials.gov
Start Date
September 6, 2022
End Date
December 15, 2026
Last Updated
10 months ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age 18 years or older
  • Pre-morbid proficient speaker of English
  • Diagnosis of adult-onset aphasia
  • Vision and hearing sufficient to complete assessments

Exclusion Criteria

  • No history of childhood speech or language difficulties
  • No history of major psychiatric illness, cognitive impairment, or neurological disorders such as seizures

Outcomes

Primary Outcomes

Reading Comprehension Battery for Aphasia-2 (RCBA-2; LaPointe & Horner, 1998) Scores

Time Frame: 1-week after intervention

To determine if group participation improves intervention-specific language skills in reading comprehension by comparing baseline score to 1-week post-intervention score

Secondary Outcomes

  • Communication Confidence Rating Scale for Aphasia (CCRSA; Babbitt & Cherney, 2010)(1-week post-intervention)
  • Discourse Production Task(1-week post-intervention)
  • Patient Reported Outcomes Measurement Information System (PROMIS)(1-week post-intervention)
  • Gray Oral Reading Test (GORT; Wiederholt & Bryant, 2012)(1-week post-intervention)
  • Writing of Untrained Control Words (non-standardized).(1-week post-intervention)

Study Sites (1)

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