Primary Progressive Aphasia G31.0 F02.0
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: PPA diagnosis according to the consensus criteria of Gorno-Tempini (2011), all variants of PPA (logopenic variant, semantic variant and agrammatic variant) Group ability Ability to consent Intact visual acuity / sufficient acoustic comprehension (with hearing aid / visual aid)
Exclusion criteria
Exclusion criteria: Severe depressive symptoms (>35 points in the MADRS) Pronounced cognitive deficits (<10 points in the MMSE)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improving the quality of life: - 39-item version of the Stroke and Aphasia Quality of Life Scale (SAQOL-39, Hilari et al., 2003) Measurement times: t0, t1, t2, t3 | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in cognitive and linguistic functions: - Satisfaction with Life Scale (SWLS, Diener et al., 1985); aim: to measure life satisfaction, also in contrast to quality of life; measurement times: t0, t1, t2, t3 - Montgomery-Asberg Depression Scale (MADRS, Davidson et al., 1986); aim: to measure depression, also in relation to quality of life; measurement times: t0, t1, t2, t3 - Mini-Mental Status Test (MMST, Folstein et al., 1975); aim: to assess cognitive abilities; measurement times: t0, t1, t2, t3 - Scenario Test (ST, Nobis-Bosch, 2020); aim: to assess communicative-pragmatic abilities; measurement times: t0, t1, t2, t3 - Visual Analogue Scale (VAS, Ushijima et al., 2006); aim: to assess the mood of the participants; measurement times: before and after the 1st and 5th individual therapy sessions; after the 1st and 7th group therapy sessions - Semi-structured interview after the intervention; aim: to record attitudes towards / experiences with the intervention provided; measurement time: after the intervention - Fidelity checklist (self-rating); objective: self-reflection with regard to adherence to the customised Narraktiv® protocol after each individual and group therapy session - Fidelity checklist (independent rating); objective: quality assurance; evaluation of treatment adherence to the adapted Narraktiv® protocol after completion of the study in a randomised sample of 10% of the video recordings; measurement time: after completion of the study | — |
Countries
Germany
Contacts
Universitätsmedizin