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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
University of Malaga
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring education, physiotherapy

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    February 9, 2016
    Last Updated
    September 27, 2019
    Sponsor
    University of Malaga
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    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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