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Regaining Confidence After Stroke a Feasibility Randomised Controlled Trial

Evaluating the Feasibility of a Regaining Confidence After Stroke Course (RCAS) to Facilitate Adjustment for People With Stroke Discharged From Rehabilitation.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03807284
Acronym
RCAS
Enrollment
51
Registered
2019-01-16
Start date
2013-04-01
Completion date
2016-08-31
Last updated
2019-01-25

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

Conditions

Stroke

Keywords

Feasibility, Confidence, group intervention, Psycho-social intervention, Stroke recovery

Brief summary

The Regaining Confidence after Stroke Course (RCAS) is a group therapy intervention to evaluate the feasibility of conducting a definitive trial, aimed to facilitate adjustment for people with stroke discharged from rehabilitation, compared with usual care. The study also aimed to evaluate the feasibility of improving mood and coping in carers of the course participants.

Detailed description

The Regaining Confidence after Stroke Course (RCAS) is an is an eleven week group intervention that is designed to help stroke survivors when they have finished rehabilitation to improve confidence in daily life. This feasibility study aimed to evaluate the acceptability of the course in improving confidence, mood, adjustment and increasing activity levels in stroke survivors as well as improving mood and coping in their carers.

Interventions

BEHAVIORALA group psychosocial course

A 2 hour, weekly group psychosocial therapy RCAS course that aims to improve confidence and help adjustment after a stroke.

Sponsors

National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
University of Nottingham
Lead SponsorOTHER

Study design

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

Masking description

The outcome assessor was masked to the intervention until the outcomes were complete.

Intervention model description

A parallel group two arm feasiblity randomised controlled trial with 1:1 allocation in a single centre, comparing eleven week RCAS Course in addition to usual care, to usual care alone.

Eligibility

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

Inclusion criteria

* A clinical diagnosis of stroke within two years * Discharged from all other rehabilitation therapies * Not involved in trials of other psychological interventions * Not previously attended an RCAS course

Exclusion criteria

* Score of \<10 on the Barthel Index (sufficiently independent to cope in a group setting) * Score \<8 on the Sheffield Screening test for Acquired Language Disorders so that participants would be able to understand the materials being presented * Unable to speak English * Unable to give informed consent

Design outcomes

Primary

MeasureTime frameDescription
Number of participants recruited to the trialOne year recruitment periodNumber of participants recruited to the trial
Number of participants who completed the trialEnd of StudyNumber of participants who completed the trial

Secondary

MeasureTime frameDescription
Level of ConfidenceBaseline, 3 and 6 months follow upA Confidence after Stroke (53 item) measure. This measure uses a Likert type format with four 'Likert type' responses, from zero to three depending on a positive or negative worded item. The highest achievable score of 159 indicating a high level of confidence.
MoodBaseline, 3 and 6 months follow upGHQ-30. Mood is measured using 30 questions, each with four response scores (0=better than usual) (1= about the same) (2 =Less well than usual) (3=Much less well than usual) maximum score is 90.
Carers strainBaseline, 3 and 6 monthsCarer Strain Index. The measure consists of 13 questions with yes or no answers. Highest score of 13 is achievable, where a high score indicates increased carer strain
CopingBaseline, 3 and 6 months follow upThe COPE inventory (Coping Orientation for Problem Orientated Experiences) a 60 question measure which asks how participants deal with stress and what they do in stressful events. The inventory has 15 domains and a maximum score of 16 is achievable. A high score indicates more frequent use of the described coping strategy
ActivityBaseline, 3 and 6 months follow upNottingham Extended Activity of Daily Living Scale. A ranked self-assessment of important activities after following a stroke. Scale is ranked from 0-22.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026