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Delivering Group Support for People With Aphasia Through Eva Park

Delivering Group Support for People With Aphasia Through Eva Park

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03115268
Enrollment
32
Registered
2017-04-14
Start date
2017-05-16
Completion date
2019-04-15
Last updated
2019-08-06

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

Conditions

Aphasia

Keywords

social support

Brief summary

The project will investigate the feasibility and acceptability of a remote support group intervention for people with aphasia, and will investigate the impact of that intervention on measures of wellbeing, quality of life and communication. The intervention will be delivered to 32 participants in Eva Park, a virtual island specifically designed for people with aphasia.

Interventions

BEHAVIORALSocial support groups delivered in EVA Park

Intervention will comprise support group meetings delivered in EVA Park, a virtual island created for people with aphasia. Scheduled meetings will be held every two weeks, led by the group co-ordinator and volunteers. Participants will have unlimited access to EVA Park, so will be able to meet up with other group members between meetings.

Sponsors

The Stroke Association, United Kingdom
CollaboratorOTHER
City, University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

* Stroke survivor with aphasia; Score within the aphasic range on the Frenchay Aphasia Screening Test (FAST); Fluent pre-stroke user of English.

Exclusion criteria

* Co-morbidity affecting cognition; Severe hearing or visual impairments

Design outcomes

Primary

MeasureTime frameDescription
Pre to post intervention change on the Warwick Edinburgh Mental Well-being Scale (WEMWBS)At randomisation and at 7 and 14 months post randomisationA 14 item questionnaire about feelings of wellbeing
Pre to post intervention change on the Communication Activities of Daily Living test (CADL-2)At randomisation and at 7 and 14 months post randomisationA 50 item standardized test of everyday communication activities, designed for people with aphasia

Secondary

MeasureTime frameDescription
Pre to post intervention change on the Social Connectedness Scale - Revised (Lee et al. 2001)At randomisation and at 7 and 14 months post randomisationA 20 item questionnaire about feelings of social connectedness
Pre to post intervention change on The Western Aphasia Battery - Revised (Kertesz, 2007)At randomisation and at 7 and 14 months post randomisationA standardized assessment of language impairment designed for people with aphasia
Pre to post intervention change on the Stroke and Aphasia Quality of Life measure (SAQOL-39) (Hilari et al, 2003)At randomisation and at 7 and 14 months post randomisationA self reporting questionnaire about health related quality of life designed for people with stroke and aphasia

Other

MeasureTime frameDescription
Participant recruitment and attrition ratesThroughout recruitment, intervention and follow up period, up to 14 monthsThe number of participants referred to the project and the proportion who consent; the number of individuals lost to follow up
Treatment costThroughout intervention periods; Months 1 - 6 for the immediate arm; Months 8 - 13 for the waitlist control arm.Logs of all costs associated with the intervention, relating to: Human Resources, Technical costs, Materials, Capital costs and Travel
Participant views about interventionInterviews conducted up to 4 weeks post intervention (Month 7 for immediate arm; month 14 for waitlist control arm)Responses to in-depth semi-structured interviews conducted with all participants post intervention
Group coordinators' and volunteers' views about interventionAt month 7 for the immediate arm; at month 14 for the waitlist control armResponses to in-depth semi-structured interviews conducted with all coordinators and 8 purposefully selected volunteers
Qualitative findings from Human Computer Interaction AssessmentsConducted in the first and last week of intervention; Months 1 and 6 for the immediate arm; Months 8 and 13 for the waitlist control arm.Structured observations and interviews conducted with 8 randomly selected participants from each arm, aiming to determine the suitability of EVA Park for delivering support group meetings
Time spent using EVA Parkthroughout intervention periods; Months 1 - 6 for the immediate arm; Months 8 - 13 for the waitlist control armAutomatic log data of each participant's usage of EVA Park

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026