A Stepped-wedge Cluster Randomized Controlled Trial for Evaluating an Intervention in Patients With Stroke Tailored Education in Addition to Physiotherapist Treatment
Primary Purpose
Stroke
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Multimodal intervention
Sponsored by

About this trial
This is an interventional treatment trial for Stroke focused on measuring education, physiotherapy
Eligibility Criteria
Inclusion Criteria:
- The study subjects were all patients who had been hospitalised in 8 regional hospitals of Andalusian Health Service with acute cerebral stroke, clinically stable, presented an ischaemic or haemorrhagic aetiology and clinical symptoms of hemiplegia, were selectioned to receiving physiotherapy in hospitalisation, were assisted by a caregiver, had an adequate understanding of Spanish, and had given their written informed consent.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Arm Type
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Experimental
Arm Label
Group1
Group2
Group3
Group4
Group5
Group6
Group7
Group8
Arm Description
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Educational advice + physiotherapist treatment
Outcomes
Primary Outcome Measures
Canadian Neurological Scale (CNS):
Measures neurological status of stroke (psychometric properties: Spearman correlation coefficient of 0.924 (95% CI: 0.896-0.951) and internal consistency by Cronbach's alpha of 0.792, N=155
Secondary Outcome Measures
Trunk Control Test (TCT):
scores trunk control (psychometric properties: inter-rater reliability by Spearman's correlation coefficient r=0.76; internal consistency by Cronbach's alpha 0.83-0.86).
Motricity index (MI) of the lower and upper limbs
measures upper and lower limb strength (Spearman's correlation coefficient of 0.87 (p<0.001) for MI-LL, and of 0.88 (p<0.001) for MI-UL).
Barthel Index (BI)
scores the patient's ability to perform activities of daily living (ADL) (inter-observer reliability by Kappa indices 0.47-1.00; intra-observer reliability by Kappa indices 0.84-0.972; internal consistency by Cronbach's alpha 0.86-0.92).
Stroke Impact Scale-16 (SIS-16):
measures the deficits and physical limitations provoked by stroke (ADL, mobility and hand function) (internal consistency by Cronbach's alpha 0.87-0.95).
Modified Rankin Scale (MRS)
to score the incapacity of the patient (inter-observer reliability by Kappa indices (k=0.56 to k=0.78). Good test-re-test reliability (k=0.81 to k=0.95).
Multidimensional Scale of Perceived Social Support (MSPSS)
Full Information
NCT ID
NCT02681146
First Posted
February 9, 2016
Last Updated
September 27, 2019
Sponsor
University of Malaga
1. Study Identification
Unique Protocol Identification Number
NCT02681146
Brief Title
A Stepped-wedge Cluster Randomized Controlled Trial for Evaluating an Intervention in Patients With Stroke Tailored Education in Addition to Physiotherapist Treatment
Official Title
A Stepped-wedge Cluster Randomized Controlled Trial for Evaluating an Intervention in Patients With Stroke Tailored Education in Addition to Physiotherapist Treatment
Study Type
Interventional
2. Study Status
Record Verification Date
September 2019
Overall Recruitment Status
Unknown status
Study Start Date
January 1, 2020 (Anticipated)
Primary Completion Date
March 2022 (Anticipated)
Study Completion Date
February 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Malaga
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A stepped-wedge cluster design will be used, with the duration of the trial being 50 weeks. The 'stepped-wedge ' cluster randomised trial is a form of cross-over design with unidirectional cross-over ( from control to experimental ) but with randomisation of when each cluster undertakes this transition. In the stepped-wedge design, there is a staggered roll-out of the intervention, where the time and hence the sequence of units (clusters) that will start the intervention at each period is determined by random allocation.
The randomisation occurs before the start of the trial. All clusters start the trial in a control phase with no intervention being delivered at any site, then sequentially cross over from the control group to the intervention group, until all sites are receiving the intervention. Outcomes are measured on the study participants in all clusters at every time period, hence measurement of outcomes takes place at each step in the wedge; each cluster provides data points in the control and intervention conditions allowing each site to act as its own control.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
education, physiotherapy
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
320 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Group1
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group2
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group3
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group4
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group5
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group6
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group7
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Arm Title
Group8
Arm Type
Experimental
Arm Description
Educational advice + physiotherapist treatment
Intervention Type
Other
Intervention Name(s)
Multimodal intervention
Intervention Description
Educational advice + physiotherapist treatment
Primary Outcome Measure Information:
Title
Canadian Neurological Scale (CNS):
Description
Measures neurological status of stroke (psychometric properties: Spearman correlation coefficient of 0.924 (95% CI: 0.896-0.951) and internal consistency by Cronbach's alpha of 0.792, N=155
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Trunk Control Test (TCT):
Description
scores trunk control (psychometric properties: inter-rater reliability by Spearman's correlation coefficient r=0.76; internal consistency by Cronbach's alpha 0.83-0.86).
Time Frame
8 weeks
Title
Motricity index (MI) of the lower and upper limbs
Description
measures upper and lower limb strength (Spearman's correlation coefficient of 0.87 (p<0.001) for MI-LL, and of 0.88 (p<0.001) for MI-UL).
Time Frame
8 weeks
Title
Barthel Index (BI)
Description
scores the patient's ability to perform activities of daily living (ADL) (inter-observer reliability by Kappa indices 0.47-1.00; intra-observer reliability by Kappa indices 0.84-0.972; internal consistency by Cronbach's alpha 0.86-0.92).
Time Frame
8 weeks
Title
Stroke Impact Scale-16 (SIS-16):
Description
measures the deficits and physical limitations provoked by stroke (ADL, mobility and hand function) (internal consistency by Cronbach's alpha 0.87-0.95).
Time Frame
8 weeks
Title
Modified Rankin Scale (MRS)
Description
to score the incapacity of the patient (inter-observer reliability by Kappa indices (k=0.56 to k=0.78). Good test-re-test reliability (k=0.81 to k=0.95).
Time Frame
8 weeks
Title
Multidimensional Scale of Perceived Social Support (MSPSS)
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
The study subjects were all patients who had been hospitalised in 8 regional hospitals of Andalusian Health Service with acute cerebral stroke, clinically stable, presented an ischaemic or haemorrhagic aetiology and clinical symptoms of hemiplegia, were selectioned to receiving physiotherapy in hospitalisation, were assisted by a caregiver, had an adequate understanding of Spanish, and had given their written informed consent.
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34813082
Citation
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Results Reference
derived
Learn more about this trial
A Stepped-wedge Cluster Randomized Controlled Trial for Evaluating an Intervention in Patients With Stroke Tailored Education in Addition to Physiotherapist Treatment
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