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Getting Out of The House: a multicentre trial to evaluate an outdoor mobility intervention for people who have had a stroke

A multicentre randomised controlled trial of rehabilitation aimed at improving outdoor mobility for people who have had a stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN58683841
Enrollment
676
Registered
2009-02-09
Start date
2009-08-01
Completion date
Unknown
Last updated
2018-01-08

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

A novel rehabilitation technique (intervention) group will be compared to a usual care (control) group: Intervention group: Specifically designed outdoor mobility training and practice with a skille

Sponsors

University of Nottingham (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Amended as of 12/03/2010: Point 2 below has been amended to read as follows: 2. At least six weeks since stroke Amended as of 15/09/2009: 1. Age 18 years or over 2. At least six weeks but no longer than five years since stroke 3. Wishing to get out of the house more often 4. The participant must give informed consent before completing any study-related procedure, which means any assessment or evaluation that would not have formed part of their normal care. Amended as of 13/07/2009: 1. Aged 18 years or over, either sex 2. At least six weeks but no longer than five years since stroke 3. Wishing to get out of the house more often 4. Able to comply with the requirements of the protocol and therapy programme 5. The participant must give informed consent before completing any study-related procedure, which means any assessment or evaluation that would not have formed part of their normal care Initial information at time of registration: 1. Both males and females, aged 18 years or over 2. At least six weeks since stroke 3. Wishing to get out of the house more often 4. Able to comply with the requirements of the protocol and therapy programme 5. The participant or legal representative must give informed consent before completing any study-related procedure, which means any assessment or evaluation that would not have formed part of their normal care

Exclusion criteria

Exclusion criteria: Amended as of 15/09/2009: 1. Not able to comply with the requirements of the protocol and therapy programme, in the opinion of the assessor 2. Still in post-stroke intermediate care or active rehabilitation 3. Previous enrolment in this study Amended as of 13/07/2009: 1. Significant cognitive impairment which will impede ability to complete the assessments 2. Diagnosis likely to interfere with rehabilitation or outcome assessments e.g. terminal illness 3. Still in post-stroke intermediate care or active rehabilitation 4. Previous enrolment in this study Initial information at time of registration: 1. Significant cognitive impairment which will impede ability to complete the assessments 2. Diagnosis likely to interfere with rehabilitation or outcome assessments e.g. terminal illness 3. Previous enrolment in this study

Design outcomes

Primary

MeasureTime frame
Social Function domain of the health related quality of life measure SF-36v2™ Health Survey at 6 months.

Secondary

MeasureTime frame
The following will be assessed at 6 and 12 months: 1. Functional ability, measured by the Nottingham Extended Activities of Daily Living Scale 2. Mobility using the Rivermead Mobility Index 3. Modified 15/09/09: The number of journeys (travel diaries) - was previously: The number and duration of journeys from the travel diaries 4. Satisfaction with outdoor mobility, assessed using one yes/no question: "Do you get out of the house as much as you would like?" 5. Mood, using the General Health Questionnaire 12 6. Carer psychological distress, measured using the General Health Questionnaire 12pt 7. EuroQol EQ-5D 8. Resource use of health and social care 9. Provision of equipment 10. Participant mortality will be collected from medical records

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 26, 2026