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| Name | Class |
|---|---|
| National Institute for Health Research, United Kingdom | OTHER_GOV |
| University Hospital Southampton NHS Foundation Trust | OTHER |
| Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust | OTHER_GOV |
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When a person has had a stroke they often lose their confidence, motivation and the ability to move one arm and hand. Recent research has shown that intensive exercise assists recovery of movement, but people are often discouraged by slow progress and stop using their weak limb.
A new idea, called Constraint Induced Therapy (CIT), has been shown to overcome this habitual 'non-use'. CIT involves wearing a mitt on the unaffected hand for several hours a day to prevent it from being used. Use of the weak arm and hand is encouraged by intensive exercises. CIT is not available in the NHS because of lack of therapist time for supervision and patients lack the confidence and motivation to carry out CIT alone at home.
This study will have two stages.
Stage 1.
The aim of this part of the study is to develop a web-based therapy programme ('LifeCIT') to support patients carrying out CIT at home (with their carer where possible) with online therapist support. The investigators will develop the therapy programme working closely with at least 12 patients, 6 carers and 6 therapists to identify and resolve any problems.
Stage 2
The investigators will then carry out a pilot trial in 6 treatment centers with 20 patients who have just been discharged from hospital and who have loss of arm and hand function. To test LifeCIT the investigators will randomly allocate patients to receive either the LifeCIT intervention or usual care. A researcher, who doesn't know which group patients have been allocated to, will measure their arm and hand function, record the problems this causes and how it affects their quality of life. Tests will be repeated after treatment (3 weeks) and 6 months later. The investigators will also examine the cost-effectiveness of treatment and ask both therapists and patients for their views.
Development and pilot evaluation of a web-supported programme of Constraint Induced Therapy following stroke (LifeCIT) PB-PG-0909-20145
Jane H. Burridge PhD1, Claire Meagher MSc1, Ann-Marie Hughes PhD1, Sean-Ewings PhD2, Ana-Carolina Gonçalves BSc1, Claudia H. S. Alt PhD1, Sebastien Pollet BSc1, Lucy Yardley PhD3
Lay Summary
Background:
Following stroke people often lose their motivation and ability to move their hemiplegic arm. Intensive exercise assists recovery, but people often get into the habit of not using their arm.
Constraint-Induced Therapy (CIT) overcomes this habitual 'non-use'. CIT involves wearing a mitt on the unaffected hand to prevent it from being used. Use of the weak arm is encouraged by intensive exercises. CIT is not generally available in the NHS because of lack of therapist time to supervise the intensive exercises. We found that patients lack the confidence and motivation to carry out CIT alone at home.
We developed a web-based therapy programme ('LifeCIT') to support patients carrying out CIT at home with online therapy support. We developed LifeCIT working closely with patients, their carers and therapists. Their feedback and ideas ensured LifeCIT satisfied their needs. The first working version of LifeCIT was tested with 12 patients who had recently had a stroke and their feedback was used to make further improvements. A pilot trial with 19 patients tested whether LifeCIT affected recovery. We randomly allocated each patient to receive either 'LifeCIT' or 'usual care'. We tested patients before the study and repeated measurements after treatment (3 weeks) and 6 months later. We asked the patients who had used LifeCIT for their views on it - what was good and bad, and whether it had affected their ability to use their arm and hand.
Summary of research
Background:
Conventional therapy to improve upper limb function following stroke is not effective. <50% of people who survive a stroke but have moderate to severe hemiparesis regain upper limb function. Learnt non-use has been identified as an important factor in poor recovery. Constraint-Induced Therapy (CIT) [1; 2], proposes that constraint of the unaffected arm and hand, coupled with intensive training of the hemiplegic limb, leads to behavioral changes towards greater use of the hemiplegic limb, neuroplastic cortical changes and the return of function [3].
Despite evidence from a large RCT (n=222), which showed improvement in function maintained at 12 months post-treatment [4], CIT has not translated into clinical practice, due partly to the cost of intensive (minimum 4 hours/day for 10 days) one-to-one treatment. An alternative approach in which CIT was used at home without intensive therapy showed in an A-B-A trial, but patients reported lack of motivation to wear the C-MIT (Constraint Mitt) and comply with the exercise programme [5].
LifeGuide is a set of software resources to create and modify programmes of personalized online support for therapy, without the need for costly dedicated programming. It was used in this study to address the motivational barriers to home-based CIT.
Aims and Objectives:
Working with patients, carers and therapists, create an accessible and engaging web-supported programme of CIT for home-based upper limb stroke rehabilitation - LifeCIT.
Conduct a Phase II single-blinded RCT of LifeCIT to:
Methods:
Phase 1. Intervention development:
The LifeCIT web-based programme for CIT combined with personalized activities, automated progress-relevant advice intervention content and format was co-designed with patients, carers and healthcare professionals. We held a series of meetings in which participants were shown mock-up webpages. Pages, structure, content, and activities were revised through a systematic response to feedback and then further revisions were made through in-depth think-aloud sessions with four chronic stroke patients.
During the development, process tape-recorded interviews and observational ('think aloud') studies [6-8] were used. Data collection and analysis was concurrent with intervention development, allowing immediate modification and re-testing of intervention components as potential improvements were identified.
The prototype web-based programme was then trialed with 12 sub-acute patients and their carers/ healthcare professionals and further revisions were made. The final version of the web-support programme was designed to:
Phase II Clinical trial:
A 6-center 3-week pilot trial compared usual care with LifeCIT. Computer block-randomization stratified into three ability groups. Participants randomized to the LifeCIT group were asked to wear the C-MIT for between 6 and 9 waking hours and aim for up to 6 hours activities per day on 5 days/week. A programme of activities was designed with them.
Participants Two cohorts of participants were recruited: One, sub-acute patients following discharge from hospital and one of the participants who had experienced a stroke more than 16 weeks previously.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| LifeCIT | Experimental | Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. |
|
| Standard Care | Active Comparator | Participants received their usual care which included home exercises |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| LifeCIT | Behavioral | Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Upper Limb Impairment: Motor Activity Log (MAL) Amount of Use (AOU) | The MAL comprises 28 functional items, (e.g. picking up a glass; turning a key to open the door) each item is assessed by self-report on a six-point ordinal scale (0-5). Participants are asked to rate the amount of use of their hemiplegic arm for each item. Zero is scored if they have not used their affected arm, five is scored when they use their affected as often as before their stroke occurred. The final MAL score is calculated as a mean score of the individual items. The minimum and maximum mean scores are 0-5, with higher values representing better outcomes. | Baseline, Post intervention (three weeks) and 6 months |
| Change From Baseline in Upper Limb Impairment: Motor Activity Log (MAL) Quality of Use (QOU) | he MAL comprises 28 functional items, (e.g. picking up a glass; turning a key to open the door) each item is assessed by self-report on a six-point ordinal scale (0-5). Participants are asked to rate the quality of use of their hemiplegic arm for each item. Zero is scored if they can not use their affected arm, five is scored when they can use their affected arm as well as before their stroke occurred. The final MAL score is calculated as a mean score of the individual items. The minimum and maximum mean scores are 0-5, with higher values representing better outcomes. | Baseline, Post Intervention (three weeks) and 6 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Upper Limb Function: Wolf Motor Function Test (WMFT) Functional Ability Scale (FAS) | The modified WMFT is a valid, widely used measure that scores performance of activities of daily living in a controlled and structured environment he test has 17 items which test a range of functional upper limb tasks (for example turning a key in a lock, folding a towel, retrieving a weight). Each item is scored by the time taken to complete the task, the weight lifted or hand strength as measured by a hand held goniometer. Each item is subsequently scored on a rating scale 'The Functional Ability Scale' (FAS) from 0-5. Zero is scored if the participant does not attempt the task with their hemiplegic arm, and five is scored if the task is completed with a normal movement. The mean score of all items results with a mean FAS score. |
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Inclusion Criteria:
Exclusion Criteria:
People for whom communication problems prevent effective use of the system, will be excluded unless they have a carer who can support them effectively.
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| Name | Affiliation | Role |
|---|---|---|
| Jane Burridge, PhD | Professor at University of Southampton | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Southampton | Southampton | United Kingdom |
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| ID | Title | Description |
|---|---|---|
| FG000 | LifeCIT | Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. LifeCIT: Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. |
| FG001 | Standard Care | Standard Care: Participants will receive their usual care from their NHS provider. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | LifeCIT | Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. LifeCIT: Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Change in Upper Limb Impairment: Motor Activity Log (MAL) Amount of Use (AOU) | The MAL comprises 28 functional items, (e.g. picking up a glass; turning a key to open the door) each item is assessed by self-report on a six-point ordinal scale (0-5). Participants are asked to rate the amount of use of their hemiplegic arm for each item. Zero is scored if they have not used their affected arm, five is scored when they use their affected as often as before their stroke occurred. The final MAL score is calculated as a mean score of the individual items. The minimum and maximum mean scores are 0-5, with higher values representing better outcomes. | Posted | Mean | Standard Deviation | units on a scale | Baseline, Post intervention (three weeks) and 6 months |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | LifeCIT | Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. LifeCIT: Participants will be asked to aim to wear the C-MIT for 9 hours a day for 5 days/week, including 4-6 hours of structured activities per day: two 30-60 minute sessions of web-based activities and 3-4 hours practicing everyday activities. |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Hip fracture | Musculoskeletal and connective tissue disorders | Participant fell off side of bed before starting LifeCIT intervention - unrelated |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Frozen Shoulder | Musculoskeletal and connective tissue disorders |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Jane Burridge | University of Southampton | +44(0)2380 598 885 | jhb1@soton.ac.uk |
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| ID | Term |
|---|---|
| D020521 | Stroke |
| ID | Term |
|---|---|
| D002561 | Cerebrovascular Disorders |
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D059039 | Standard of Care |
| ID | Term |
|---|---|
| D019984 | Quality Indicators, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
| D017530 | Health Care Quality, Access, and Evaluation |
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| Standard Care | Behavioral | Participants will receive their usual care from their NHS provider. |
|
| Baseline, Post intervention (three weeks), 6 months |
| Change in Upper Limb Impairment: Fugel Myer Upper Extremity (FMUE) | The upper extremity domain of the Fugel Myer is a 0-66 point clinical assessed scale where separate Items are scored on a 3-point ordinal scale: 0 = cannot perform, 1 = performs partially, 2 = performs fully. A higher score indicates indicates an increased level of function. | Baseline, Post Intervention (three weeks) and 6 months |
| Change in Occupational Performance: Canadian Occupational Performance Measure Performance (COPM) | The Canadian Occupational Performance Measure (COPM) is an individualized client-centered measure designed for use by therapists to detect a change in a client's self-perception of occupational performance over time. The COPM involves a 5-step process within a semi-structured interview conducted by a therapist. The Interview focuses on identifying activities within each performance domain that the client wants, needs, or is expected to perform. They are then asked to rate their performance and satisfaction from 0-10 for each activity identified. A score of 0 indicates they are unable to perform the activity and a score of 10 means they can complete the activity. The same scoring system is used for the COPM Satisfaction assessment with scores ranging from 0-10 and higher scores indicating greater satisfaction. | Baseline, Post intervention (three weeks) and 6 months |
| BG001 | Standard Care | Standard Care: Participants will receive their usual care from their NHS provider. |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| OG001 | Standard Care | Standard Care: Participants will receive their usual care from their NHS provider. |
|
|
| Primary | Change From Baseline in Upper Limb Impairment: Motor Activity Log (MAL) Quality of Use (QOU) | he MAL comprises 28 functional items, (e.g. picking up a glass; turning a key to open the door) each item is assessed by self-report on a six-point ordinal scale (0-5). Participants are asked to rate the quality of use of their hemiplegic arm for each item. Zero is scored if they can not use their affected arm, five is scored when they can use their affected arm as well as before their stroke occurred. The final MAL score is calculated as a mean score of the individual items. The minimum and maximum mean scores are 0-5, with higher values representing better outcomes. | Posted | Mean | Standard Deviation | units on a scale | Baseline, Post Intervention (three weeks) and 6 months |
|
|
|
| Secondary | Change in Upper Limb Function: Wolf Motor Function Test (WMFT) Functional Ability Scale (FAS) | The modified WMFT is a valid, widely used measure that scores performance of activities of daily living in a controlled and structured environment he test has 17 items which test a range of functional upper limb tasks (for example turning a key in a lock, folding a towel, retrieving a weight). Each item is scored by the time taken to complete the task, the weight lifted or hand strength as measured by a hand held goniometer. Each item is subsequently scored on a rating scale 'The Functional Ability Scale' (FAS) from 0-5. Zero is scored if the participant does not attempt the task with their hemiplegic arm, and five is scored if the task is completed with a normal movement. The mean score of all items results with a mean FAS score. | Posted | Mean | Standard Deviation | units on a scale | Baseline, Post intervention (three weeks), 6 months |
|
|
|
| Secondary | Change in Upper Limb Impairment: Fugel Myer Upper Extremity (FMUE) | The upper extremity domain of the Fugel Myer is a 0-66 point clinical assessed scale where separate Items are scored on a 3-point ordinal scale: 0 = cannot perform, 1 = performs partially, 2 = performs fully. A higher score indicates indicates an increased level of function. | Posted | Mean | Standard Deviation | units on a scale | Baseline, Post Intervention (three weeks) and 6 months |
|
|
|
| Secondary | Change in Occupational Performance: Canadian Occupational Performance Measure Performance (COPM) | The Canadian Occupational Performance Measure (COPM) is an individualized client-centered measure designed for use by therapists to detect a change in a client's self-perception of occupational performance over time. The COPM involves a 5-step process within a semi-structured interview conducted by a therapist. The Interview focuses on identifying activities within each performance domain that the client wants, needs, or is expected to perform. They are then asked to rate their performance and satisfaction from 0-10 for each activity identified. A score of 0 indicates they are unable to perform the activity and a score of 10 means they can complete the activity. The same scoring system is used for the COPM Satisfaction assessment with scores ranging from 0-10 and higher scores indicating greater satisfaction. | Posted | Mean | Standard Deviation | units on a scale | Baseline, Post intervention (three weeks) and 6 months |
|
|
|
| 1 |
| 11 |
| 0 |
| 11 |
| EG001 | Standard Care | Standard Care: Participants will receive their usual care from their NHS provider. | 1 | 8 | 1 | 8 |
|
| Second stroke | Nervous system disorders | Participant experienced stroke symptoms and was re-admitted to hospital |
|
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| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| COPM Satisfaction change baseline to three weeks |
|
| COPM Satisfaction change baseline to six months |
|