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Rehabilitation Training After Stroke (ReTrain)

Primary Purpose

Stroke

Status
Completed
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
Rehabilitation
Sponsored by
University of Exeter
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Primary clinical diagnosis of stroke (assessed by referring clinician/GP records)
  • >1 month (but no upper limit) since discharge from NHS physical rehabilitation services at randomisation
  • Able to walk independently indoors with or without mobility aids, but has self-reported difficulty or requires help on stairs, slopes or uneven surfaces (assessed by recruiting team using standard tools)
  • Willingness to be randomised to either control or ReTrain (and attend the training venue)
  • Cognitive capacity and communication ability sufficient to participate in the study (assessed by recruiting team using standard tools).24 NB: Criterion (3) has been selected pragmatically to maximise eligibility while ensuring participants have a mobility deficit that could be addressed by the intervention. Eligible people with aphasia will not be excluded.

Exclusion Criteria:

  • <18 years old
  • Contraindications to moderate to vigorous physical activity. Used in GP screening assessment form. (Adapted from ACSM guidelines 25) Contraindications include:

    • Acute or uncontrolled heart failure
    • Unstable or uncontrolled angina
    • Uncontrolled cardiac dysrhythmia causing symptoms or haemodynamic compromise
    • Symptomatic severe aortic stenosis
    • Current deep vein thrombosis, pulmonary embolus or pulmonary infarction
    • Acute myocarditis or pericarditis
    • Suspected or known dissecting aneurysm
    • Unstable / uncontrolled blood pressure
    • Systolic blood pressure > 160
    • Diastolic blood pressure > 100
    • Acute systemic infection
    • Uncontrolled diabetes

Sites / Locations

  • University of Exeter Medical School

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Rehabilitation training

Control

Arm Description

ReTrain: an exercise-based functional training programme comprising two phases: (1) weekly supervised sessions; (2) monthly drop-in sessions, plus home-based exercise in each phase. Week 1: one-to-one consultations with trainer to introduce programme, assess individual's concerns and capabilities, introduce and negotiate initial goals Weeks 2-11: bi-weekly 90 minute group class with group-based activities and one-to-one coaching, based on ongoing goal negotiation review and progression. Week 12: one-to-one consultations with trainer to review goals and plan ongoing unsupervised exercise programme Weeks 13-24: monthly drop-in sessions for one-to-one consultation, support and progression.

Control: treatment as usual plus receipt of a UK Stroke Association booklet on exercise after stroke.

Outcomes

Primary Outcome Measures

Change in Rivermead Mobility index
15-item, dichotomously scored measure of mobility disability. Fourteen items are self-report and one (standing for 10s without aids) is scored by observation
Change in Timed Up and Go Test
Objective measure of mobility, balance and locomotor performance, in which the individual is observed and timed rising from a chair, walking 3m, turning and returning to the chair
Change in Modified Patient Specific Functional Scale
Identification by individual of up to five functional tasks that are important and difficult to perform, and rating of ability to perform each task on a 0-10 scale
Change in Physical Activity Diary
Participants record the type of activity and its duration each day of the week (1-2 minutes per day to complete).
Change in Physical activity - 7-day accelerometry
Worn by individual to assess physical activity behaviour over seven days. Should take 5 minutes to fit watch and 10 minutes to post back

Secondary Outcome Measures

Fatigue Assessment Scale
10-item self-completion questionnaire in which aspects of fatigue are rated on how regularly they are experienced, using a 5-point scale
Stroke Self-efficacy Questionnaire
10-item questionnaire in which participants rate their confidence in completing some tasks that may have been difficult for them since their stroke
Exercise beliefs questionnaire
Measures attitudes to exercise by rating levels of agreement to 5 statements about what it can achieve for the individual.
Exercise self-efficacy questionnaire
Self-rating of confidence to overcome 4 personal barriers to exercise
Stroke Quality of Life
Self-rating of twelve dimensions of lifestyle and personal functioning
EQ-5D-5L
Measuring health-related quality of life and can be used for cost utility analysis
SF-12 46
Abbreviated version of the Short-Form-36 self-completion questionnaire measuring health-related quality of life. It can also be used to calculate the SF-6D, which may be used for cost utility analysis.
Service Receipt Inventory
Record of types and amount of use of health and social care resources including medication, clinical contacts, formal and informal social care. Completed by Assessor drawing on participant and family accounts, and clinical records if available.
Carer Burden Index
Carers of stroke survivors rate the difficulties and challenges of providing care
Adverse incidents
Adverse events

Full Information

First Posted
April 16, 2015
Last Updated
March 15, 2019
Sponsor
University of Exeter
Collaborators
The Stroke Association, United Kingdom
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1. Study Identification

Unique Protocol Identification Number
NCT02429180
Brief Title
Rehabilitation Training After Stroke
Acronym
ReTrain
Official Title
Community-based Rehabilitation Training After Stroke: a Pilot Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
July 31, 2015 (Actual)
Primary Completion Date
January 27, 2016 (Actual)
Study Completion Date
January 27, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Exeter
Collaborators
The Stroke Association, United Kingdom

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A pilot study that will evaluate the feasibility and acceptability of procedures to inform the design and delivery of a definitive RCT of ReTrain (which would assess the clinical and cost effectiveness of ReTrain for stroke survivors).
Detailed Description
Background and rationale Residual physical disability is common following discharge from stroke rehabilitation services. A third of first-time stroke survivors remain physically disabled five years after their stroke, equivalent to more than 300,000 people in the UK. Stroke services are traditionally "front loaded" with provision tailing off a few months after stroke. However, people with stroke report a variety of unmet long-term needs and a sense of being abandoned by NHS services. The UK National Stroke Strategy recommends that stroke be regarded as a Long Term Condition and that continuing support is provided for those who need it. This includes community-based rehabilitation, with an emphasis on personalisation, re-ablement and self-management of the consequences of stroke. There is good evidence that exercise can promote functional recovery, enhance adjustment and coping, improve psychological wellbeing, and reduce the risk of recurrence. Hence stroke guidelines recommend that people with stroke should regularly engage in specific forms of exercise, however many do not meet these recommendations. Various personal and environmental factors may account for this: stroke-related impairments, lack of confidence or knowledge regarding exercise and its benefits, and inadequate provision of support programmes and facilities. In response, community-based programmes are being offered. However, these programmes often focus on fitness rather than function, giving little attention to self-management or to sustaining behaviour (to ensure benefits are maintained after structured programmes have ended). National stroke guidelines recommend interventions address functional improvement and self-management strategies even though a recently updated Cochrane review notes the gap in evidence regarding these interventions. An approach called ARNI (Action for Rehabilitation from Neurological Injury) attempts to address these concerns; it was created specifically for people with stroke and acquired brain injury who wish to continue their functional recovery.ARNI is not a rigidly-defined programme but a set of principles and strategies tailored to individual circumstances and contexts. It is led by registered exercise professionals who have been additionally trained and accredited by the ARNI institute (http://www.arni.uk.com). In the UK, the NHS, Local Authorities and other organisations are using ARNI trainers to provide community-based training for stroke survivors. Our survey of this training included Northeast England, Lancashire, Luton and Bedfordshire, Milton Keynes, Hillingdon and Cornwall. The survey found that training has been very positively received by stroke survivors, their families and clinicians but it varied in content and delivery. Reports of benefits by the broadcaster Andrew Marr have also increased public awareness of ARNI. However the evidence for ARNI remains largely anecdotal, it may only work for a selected few and the approach is difficult to replicate. There is a need for a more detailed cohesive specification of ARNI that could be rigorously evaluated and replicated. Furthermore a stroke survivor participating in our Institution's research question generation process asked if ARNI worked but as yet there have been no randomised controlled trials (RCTs) of this intervention. Thus we have followed the Medical Research Council's framework for the development and evaluation of complex interventions and undertaken five linked preliminary studies: 1) a survey of current ARNI provision in the UK; 2) a comparison of the ARNI approach with relevant stroke practice guidelines, 3) before-and-after studies of both group-based and 4) one-to-one training and 5) focus groups conducted with our participants. From this work we have designed a programme called ReTrain (Rehabilitation Training) which is based on core ARNI principles and informed by best practice guidelines for stroke. Before undertaking a large definitive RCT of ReTrain a pilot study is needed to address issues of feasibility and acceptability. Purpose of the study ReTrain aims to improve (i) functional mobility, (ii) adherence to national guidelines on post-stroke exercise levels, and (iii) health-related quality of life, for people after stroke who have been discharged from clinical rehabilitation. A definitive RCT is required to assess the clinical and cost effectiveness of the ReTrain intervention. The purpose of this pilot study is to assess to feasibility of such a trial and to evaluate trial procedures to inform the design of a definitive trial.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rehabilitation training
Arm Type
Experimental
Arm Description
ReTrain: an exercise-based functional training programme comprising two phases: (1) weekly supervised sessions; (2) monthly drop-in sessions, plus home-based exercise in each phase. Week 1: one-to-one consultations with trainer to introduce programme, assess individual's concerns and capabilities, introduce and negotiate initial goals Weeks 2-11: bi-weekly 90 minute group class with group-based activities and one-to-one coaching, based on ongoing goal negotiation review and progression. Week 12: one-to-one consultations with trainer to review goals and plan ongoing unsupervised exercise programme Weeks 13-24: monthly drop-in sessions for one-to-one consultation, support and progression.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Control: treatment as usual plus receipt of a UK Stroke Association booklet on exercise after stroke.
Intervention Type
Other
Intervention Name(s)
Rehabilitation
Intervention Description
ReTrain: an exercise-based functional training programme comprising two phases: (1) weekly supervised sessions; (2) monthly drop-in sessions, plus home-based exercise in each phase. Week 1: one-to-one consultations with trainer to introduce programme, assess individual's concerns and capabilities, introduce and negotiate initial goals Weeks 2-11: bi-weekly 90 minute group class with group-based activities and one-to-one coaching, based on ongoing goal negotiation review and progression. Week 12: one-to-one consultations with trainer to review goals and plan ongoing unsupervised exercise programme Weeks 13-24: monthly drop-in sessions for one-to-one consultation, support and progression.
Primary Outcome Measure Information:
Title
Change in Rivermead Mobility index
Description
15-item, dichotomously scored measure of mobility disability. Fourteen items are self-report and one (standing for 10s without aids) is scored by observation
Time Frame
Baseline, 6 months, 9 months
Title
Change in Timed Up and Go Test
Description
Objective measure of mobility, balance and locomotor performance, in which the individual is observed and timed rising from a chair, walking 3m, turning and returning to the chair
Time Frame
Baseline, 6 months, 9 months
Title
Change in Modified Patient Specific Functional Scale
Description
Identification by individual of up to five functional tasks that are important and difficult to perform, and rating of ability to perform each task on a 0-10 scale
Time Frame
Baseline, 6 months, 9 months
Title
Change in Physical Activity Diary
Description
Participants record the type of activity and its duration each day of the week (1-2 minutes per day to complete).
Time Frame
Baseline, 6 months, 9 months
Title
Change in Physical activity - 7-day accelerometry
Description
Worn by individual to assess physical activity behaviour over seven days. Should take 5 minutes to fit watch and 10 minutes to post back
Time Frame
Baseline, 6 months, 9 months
Secondary Outcome Measure Information:
Title
Fatigue Assessment Scale
Description
10-item self-completion questionnaire in which aspects of fatigue are rated on how regularly they are experienced, using a 5-point scale
Time Frame
Baseline, 6 months, 9 months
Title
Stroke Self-efficacy Questionnaire
Description
10-item questionnaire in which participants rate their confidence in completing some tasks that may have been difficult for them since their stroke
Time Frame
Baseline, 9 months
Title
Exercise beliefs questionnaire
Description
Measures attitudes to exercise by rating levels of agreement to 5 statements about what it can achieve for the individual.
Time Frame
Baseline, 9 months
Title
Exercise self-efficacy questionnaire
Description
Self-rating of confidence to overcome 4 personal barriers to exercise
Time Frame
Baseline, 9 months
Title
Stroke Quality of Life
Description
Self-rating of twelve dimensions of lifestyle and personal functioning
Time Frame
Baseline, 9 months
Title
EQ-5D-5L
Description
Measuring health-related quality of life and can be used for cost utility analysis
Time Frame
Baseline, 9 months
Title
SF-12 46
Description
Abbreviated version of the Short-Form-36 self-completion questionnaire measuring health-related quality of life. It can also be used to calculate the SF-6D, which may be used for cost utility analysis.
Time Frame
Baseline, 9 months
Title
Service Receipt Inventory
Description
Record of types and amount of use of health and social care resources including medication, clinical contacts, formal and informal social care. Completed by Assessor drawing on participant and family accounts, and clinical records if available.
Time Frame
Baseline, 9 months
Title
Carer Burden Index
Description
Carers of stroke survivors rate the difficulties and challenges of providing care
Time Frame
Baseline, 9 months
Title
Adverse incidents
Description
Adverse events
Time Frame
6 months, 9 months
Other Pre-specified Outcome Measures:
Title
The type and frequency of health and allied services measured using an adapted Client Service Receipt Inventory based on the TRACS study
Description
Collection of service use data
Time Frame
0-9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Primary clinical diagnosis of stroke (assessed by referring clinician/GP records) >1 month (but no upper limit) since discharge from NHS physical rehabilitation services at randomisation Able to walk independently indoors with or without mobility aids, but has self-reported difficulty or requires help on stairs, slopes or uneven surfaces (assessed by recruiting team using standard tools) Willingness to be randomised to either control or ReTrain (and attend the training venue) Cognitive capacity and communication ability sufficient to participate in the study (assessed by recruiting team using standard tools).24 NB: Criterion (3) has been selected pragmatically to maximise eligibility while ensuring participants have a mobility deficit that could be addressed by the intervention. Eligible people with aphasia will not be excluded. Exclusion Criteria: <18 years old Contraindications to moderate to vigorous physical activity. Used in GP screening assessment form. (Adapted from ACSM guidelines 25) Contraindications include: Acute or uncontrolled heart failure Unstable or uncontrolled angina Uncontrolled cardiac dysrhythmia causing symptoms or haemodynamic compromise Symptomatic severe aortic stenosis Current deep vein thrombosis, pulmonary embolus or pulmonary infarction Acute myocarditis or pericarditis Suspected or known dissecting aneurysm Unstable / uncontrolled blood pressure Systolic blood pressure > 160 Diastolic blood pressure > 100 Acute systemic infection Uncontrolled diabetes
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sarah Dean, PhD
Organizational Affiliation
University of Exeter Medical School
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Rod Taylor, Prof
Organizational Affiliation
University of Exeter Medical School
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anne Forster, Prof
Organizational Affiliation
University of Leeds
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Anne Spencer, Prof
Organizational Affiliation
University of Exeter Medical School
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Martin James, Dr
Organizational Affiliation
Royal Devon and Exeter NHS Foundation Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Rhoda Allison, Dr
Organizational Affiliation
Torbay & Southern Devon Health & Care Trust
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Shirley Stevens, Mrs
Organizational Affiliation
PenPIG
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Meriel Norris, Dr
Organizational Affiliation
Brunel University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Leon Poltawski, Dr
Organizational Affiliation
University of Exeter Medical School
Official's Role
Study Director
Facility Information:
Facility Name
University of Exeter Medical School
City
Exeter
State/Province
Devon
ZIP/Postal Code
EX1 2LU
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
31443735
Citation
Norris M, Poltawski L, Calitri R, Shepherd AI, Dean SG; ReTrain Team. Hope and despair: a qualitative exploration of the experiences and impact of trial processes in a rehabilitation trial. Trials. 2019 Aug 23;20(1):525. doi: 10.1186/s13063-019-3633-8.
Results Reference
derived
PubMed Identifier
30049699
Citation
Norris M, Poltawski L, Calitri R, Shepherd AI, Dean SG; ReTrain Team. Acceptability and experience of a functional training programme (ReTrain) in community-dwelling stroke survivors in South West England: a qualitative study. BMJ Open. 2018 Jul 25;8(7):e022175. doi: 10.1136/bmjopen-2018-022175.
Results Reference
derived
PubMed Identifier
29449290
Citation
Dean SG, Poltawski L, Forster A, Taylor RS, Spencer A, James M, Allison R, Stevens S, Norris M, Shepherd AI, Landa P, Pulsford RM, Hollands L, Calitri R. Community-based rehabilitation training after stroke: results of a pilot randomised controlled trial (ReTrain) investigating acceptability and feasibility. BMJ Open. 2018 Feb 15;8(2):e018409. doi: 10.1136/bmjopen-2017-018409.
Results Reference
derived
PubMed Identifier
27697876
Citation
Dean SG, Poltawski L, Forster A, Taylor RS, Spencer A, James M, Allison R, Stevens S, Norris M, Shepherd AI, Calitri R. Community-based Rehabilitation Training after stroke: protocol of a pilot randomised controlled trial (ReTrain). BMJ Open. 2016 Oct 3;6(10):e012375. doi: 10.1136/bmjopen-2016-012375.
Results Reference
derived
Links:
URL
http://www.arni.uk.com/
Description
Action for rehabilitation after neurological injury
URL
http://www.exeter.crf.nihr.ac.uk/
Description
NIHR Exeter Clinical Research Facility
URL
http://clahrc-peninsula.nihr.ac.uk/
Description
PenCLAHRC

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Rehabilitation Training After Stroke

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