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A rehabilitation programme for individuals who have suffered a stroke

The psychosocial Benefits of an Innovative Community-university Rehabilitation programme for Individuals who have suffered a Stroke: a controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN52813039
Enrollment
72
Registered
2014-01-29
Start date
2014-01-15
Completion date
Unknown
Last updated
2017-02-27

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

Conditions

Stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

An independent physiotherapist provides study details and assigns individuals to groups. This study is non-randomised due to resource limitations and access. Control group: no treatment Experimenta
Elsworth et al., 2011).

Sponsors

University of Birmingham (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants: Seventy two (36 in each group) individuals from the community that have been diagnosed as having a stroke will be included. Individuals will be selected from a sample within the Birmingham area including South Birmingham and Solihull borough. Individuals will be referred to the study by different charities including the Stroke Association, Different Strokes Charity, conductive education or referred by another related charitable organisation and local stroke support groups. We will not recruit from NHS sources. Inclusion Criteria 1. Individuals must have been diagnosed with a stroke (DOH, 2010). 2. Either gender, age range 18-100 years old

Exclusion criteria

Exclusion criteria: 1. Individuals who are experiencing acute mental health symptoms or that are medically unstable will also be excluded 2. Individuals who are currently involved in a physical activity, behavioural or nutritional research trial 3. Individuals who are currently undertaking exercise within a group or within the community on more than one day a week.

Design outcomes

Primary

MeasureTime frame
Stroke self-efficacy (Jones et al., 2008), questionnaire measured by a blind assessor at two time points (at baseline and at 11 and 22 weeks).

Secondary

MeasureTime frame
1. Social identification measure (Postmes et al., 2013). 2. A 7-item falls efficacy questionnaire (Kempen et al., 2007) 3. 10-meter walk and reach and grasp Outcomes will be measured by a blind assessor at two time points (at baseline and at 11 and 22 weeks).

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026