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Reducing the impact of aphasia in stroke patients and their caregivers a year post onset via a brief early intervention: a cluster randomised control trial of the Aphasia Action Success Knowledge (ASK) program.

Reducing the psychosocial impact of aphasia on mood and quality of life in people with aphasia and the impact of caregiving in family members through the Aphasia Action Success Knowledge (Aphasia ASK) program: study protocol for a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000979651
Acronym
The ASK study
Enrollment
148
Registered
2014-09-11
Start date
2015-11-24
Completion date
2019-05-30
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 overarching aim of this study is to decrease the incidence of depressive symptoms for people with aphasia and their caregivers. The specific aims are to determine whether a tailored, early intervention program (Aphasia ASK) leads to better mood and overall quality of life outcomes than an attention control (a secondary stroke prevention intervention) at 12 months post-stroke in both patients with aphasia and their caregivers.

Interventions

The Aphasia ASK intervention consists of a face to face intervention and follow-up phone calls provided by a speech pathologist up until 12 months post stroke. The intervention is for 6 to 8 weeks for an hour each week. The topics in the intervention include a number of modules and cover a range of areas including: caregiver training (e.g. communication partner training), education (on aphasia, successful coping strategies and support services) stress management, positive adaptive strategies, sh

The Aphasia ASK intervention consists of a face to face intervention and follow-up phone calls provided by a speech pathologist up until 12 months post stroke. The intervention is for 6 to 8 weeks for an hour each week. The topics in the intervention include a number of modules and cover a range of areas including: caregiver training (e.g. communication partner training), education (on aphasia, successful coping strategies and support services) stress management, positive adaptive strategies, sharing of personal stories and developing peer-based support. The participants will be able to prioritise the order of modules based on their personal interest and needs. The prioritisation occurs during the module “getting started”. Each module is colour coded rather than numbered to assist with this process. The first session establishes the goals for the program using collaborative goal setting techniques. The goals form the basis for prioritising the modules that are covered in future weeks. For example, if the participant’s goal is to stay positive, there is a module on positive thinking that includes information about and practice on exercises for strategies which were drawn from the counselling literature. At the end of each module, further resources are recommended including community based options/programmes/resources. Goals are revisited each session. The modules are designed as a guide and should be incorporated with clinical skill and knowledge to ensure the program is person-centred. Aphasia ASK is to be delivered as individual sessions with only one participant with aphasia and their family member(s) involved at any one time. Follow-up monthly phone calls or visits (which ever method is suitable for the participants) will be made until 12 months post stroke. The follow up calls with revisit the participant goals set during the program and provide additional information and resources where necessary. An Aphasia ASK program manual has been written for the provider therapist and a separate aphasia friendly workbook has been written for the recipients. Recipients will receive the written materials prior to each session.

Sponsors

The University Of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

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

Inclusion criteria

Inclusion criteria for aphasia patients include: Onset of first stroke in the past 6 months and diagnosis of aphasia 18 years Inclusion criteria for nominated family members if able to be involved include: > 18 years Sufficient hearing level and English language skills to participate

Exclusion criteria

People with aphasia and their family member(s) will be excluded if they have concomitant progressive neurological conditions (for example, dementia) or a concurrent medical condition impacting on their mental health (for example, cancer) as confirmed by self-report. There are no other inclusion or exclusion criteria for family member participants. People with aphasia must present with their first incidence of post stroke aphasia and will be excluded for the following reasons: 1) aphasia as an etiology other than stroke, 2) a current psychiatric diagnosis (for example, depressive disorder or anxiety disorder confirmed by medical record), 3) current depressive symptoms upon screening with the Stroke Aphasic Depression Questionnaire Hospital Version-10 (score of 12 or more) or The Depression Intensity Scale Circles (score of 3 or more), 4) receiving treatment in a psychiatric setting, or 5) enrolled in other aphasia or depression treatment studies.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 13, 2026