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Word retrieval in primary progressive aphasia

Is a structured therapy programme aimed at improving word retrieval for people with primary progressive aphasia successful in improving naming of treated items and do gains generalize to untreated items?

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000571673
Enrollment
7
Registered
2014-05-28
Start date
2014-05-21
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The proposed research aims to investigate the effects of a self-cueing lexical retrieval therapy on seven individuals with varying language profiles, consistent with the diverse presentation of PPA. All participants will engage in an intervention designed to improve the retrieval of nouns, verbs and adjectives through the incorporation of semantic, phonological and orthographic levels of language production. Changes in accuracy of lexical retrieval of treated and control items, pre-treatment, post treatment and four weeks maintenance, will be determined for each participant. The findings will help Speech Pathologists understand the impact this type of therapy can have on the communication you need in day-to-day life. With this knowledge it is hoped that Speech Pathologists will be better equipped to help people with Primary Progressive Aphasia.

Interventions

The treatment period for each participant will span 4 weeks, in addition to two weeks of initial baseline assessment, involving two 90 minute therapy sessions per week, delivered on an individual basis. The self-cueing approach will consist of a hierarchy of semantic, phonological and orthographic cues intended to train lexical retrieval strategies and will be administered by the student researcher. 120 treatment items will be trained across the intervention period. The stimuli will consist of 1

The treatment period for each participant will span 4 weeks, in addition to two weeks of initial baseline assessment, involving two 90 minute therapy sessions per week, delivered on an individual basis. The self-cueing approach will consist of a hierarchy of semantic, phonological and orthographic cues intended to train lexical retrieval strategies and will be administered by the student researcher. 120 treatment items will be trained across the intervention period. The stimuli will consist of 10 nouns, 10 verbs and 10 adjectives. Items will be controlled across categories for frequency, length and imageability. In addition to two weekly sessions, each participant will be assigned home practice to compliment learning in therapy. This will increase the repetition of lexical retrieval, consistent with the intensity of practice principle of neural plasticity (Kleim & Jones, 2008). Homework will include picture naming of the target items in the category for that particular week. Participants will be required to complete homework for 30 minutes on the days without therapy. Each participant will be required to document on a form their completion of the homework, including details of the time, support required and number of attempts. A spouse/significant other will assist the participant during these sessions to support word retrieval and motivation.

Sponsors

Curtin University
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Individuals are required to have a working diagnosis of Primary Progressive Aphasia (PPA) or progressive language impairment, established from previous diagnostic evaluation by a neurologist. All variants of PPA and language profiles will be accepted into the study. Participants are required to have English as their first language and no significant hearing problems that may impact their participation in the intervention. Participants will be in the early to mid-stages of PPA, as determined by a mild-moderate score on the Mini Mental State Examination (MMSE, Folstein, Folstein, & McHugh, 1975). Participants and their spouse/carer will be required to have capacity to consent themselves to their involvement in the study.

Exclusion criteria

Unable to give informed consent to participate

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026