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Comparison of the Effectiveness of an Adapted Physical Activity Program in a Dedicated Structure to a Self-program in Patients in Chronic Phase of a Stroke (StrokAPA)

Primary Purpose

Stroke

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Adapted physical activity program
Adapted physical activity self-program
Sponsored by
Assistance Publique Hopitaux De Marseille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Stroke

Eligibility Criteria

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

Inclusion Criteria: Age greater than 18 years Left or right spastic hemiparesis after a first hemorrhagic or ischemic unilateral stroke older than 6 months Walking possible for 6 minutes Exclusion Criteria: Inability to walk without human assistance (with or without technical aids) Cognitive impairment that compromises informed consent, including inability to understand the purpose and terms of the protocol Inability to communicate Presence of an additional neurological disorder Medical conditions that contraindicate physical activity, such as an unbalanced cardiovascular or respiratory condition Concurrent participation in another clinical research project

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    First APA program

    Second APA program

    Arm Description

    The evaluation of the primary endpoint to meet our main objective will be done at W13 for both groups. The addition of an APA program in autonomy following the structured program for group 1 will make it possible to answer a secondary question focusing on the comparison of the effectiveness of the self-directed program carried out alone or following a structured program. 1st group: D0: Include S1-S12: APA program at IUR Valmante S13: Break S14-S25: APA Autoprogram In addition, the patients in group 1 are maintained in the follow-up to study the maintenance of any observed effect.

    Our study design provides for compensatory participation in the structured program for patients in group 2, following the self-program. From an ethical point of view, this scheme allows all patients included in the structured APA program to benefit. 2nd group: D0: Include S1-S12: APA Autoprogram S13: End of study S14-S25: APA program at IUR Valmante compensatory

    Outcomes

    Primary Outcome Measures

    Daily activity measurement
    Measuring the number of steps per day, collected over the duration of the study, via a Stepwatch device

    Secondary Outcome Measures

    the rate physical activities in Written report
    carried out by the patient, more or less helped by his close entourage, recorded in a notebook given at the beginning of the study
    6-minute walk test (6MWT)
    A test validated in the literature that consists of measuring the greatest distance that a subject can travel on a flat surface (30 meter corridor) in 6 minutes.
    Measurement of heart rate at rest and after 6-minute walk test
    with a blood pressure cuff
    Measurement of systolic blood pressure at rest and after 6-minute walk test
    with a blood pressure cuff
    Borg Rating Scale of Exertion
    test validated in the literature that allows the evaluation of the perception of effort by the patient ; minimum value : 0 = rest : no exertion ; maximum value : 10 = maximal exertion
    Stroke Specific Quality of Life scale (SS-QoL)
    A test validated in French in the literature that assesses the specific quality of life of stroke patients in 49 items ; minimum value : 1 = Total help/ Couldn't do it at all/ Strongly agree ; maximum value : 5 = No help needed/ No trouble at all/ Strongly disagree
    Berg Balance Scale (BBS)
    validated scale allowing, by means of 14 instructions, an evaluation of balance, reproducible and sensitive to change ; minimum score : 0-20 = high risk of falling ; maximal score : 56 = no risk of falling
    Activity-specific Balanced Confidence scale (ABC scale)
    French language validated scale assessing the patient's confidence in his or her balance, using 16 situations where the subject is asked to rate his or her balance on a numerical scale ; minimal rate : 0% = not at all confident ; maximal rate : 100% = completely confident
    Behavioral regulation in exercise questionnaire
    scale used in the literature to assess motivation to perform physical activity ; minimal value : 1 = not true at all ; maximal value : 7 = absolutely true

    Full Information

    First Posted
    September 18, 2023
    Last Updated
    September 25, 2023
    Sponsor
    Assistance Publique Hopitaux De Marseille
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06061770
    Brief Title
    Comparison of the Effectiveness of an Adapted Physical Activity Program in a Dedicated Structure to a Self-program in Patients in Chronic Phase of a Stroke
    Acronym
    StrokAPA
    Official Title
    Comparison of the Effectiveness of an Adapted Physical Activity Program in a Dedicated Structure to a Self-program in Patients in Chronic Phase of a Stroke
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    December 2023 (Anticipated)
    Primary Completion Date
    January 29, 2027 (Anticipated)
    Study Completion Date
    January 29, 2027 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique Hopitaux De Marseille

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This is a prospective, randomized, controlled, two parallel arms, single-blind pilot study. In this design, all included patients in the chronic phase of a stroke will receive both modes of physical activity. This study includes patients over 18 years of age with spastic hemiparesis sequelae of a first unilateral hemispheric stroke older than 6 months and able to walk for 6 minutes. The non-inclusion criteria were the inability to walk without human assistance (with or without technical aids), the existence of cognitive disorders compromising informed consent, in particular the inability to understand the objective and the modalities of the protocol, the inability to communicate with the examiners, and the presence of an additional neurological disorder or a pathology contraindicating the practice of physical activity. The primary endpoint is based on daily activity measurement by measuring the number of steps per day, collected over the duration of the study, via a Stepwatch™ device. Secondary end points involve a written physical activity report, assessment of walking ability (via walking-test 6, heart rate, and blood pressure), a measure of perceived exertion, stroke-specific quality of life, balance, and motivation to perform physical activity.

    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
    Prevention
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    40 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    First APA program
    Arm Type
    Experimental
    Arm Description
    The evaluation of the primary endpoint to meet our main objective will be done at W13 for both groups. The addition of an APA program in autonomy following the structured program for group 1 will make it possible to answer a secondary question focusing on the comparison of the effectiveness of the self-directed program carried out alone or following a structured program. 1st group: D0: Include S1-S12: APA program at IUR Valmante S13: Break S14-S25: APA Autoprogram In addition, the patients in group 1 are maintained in the follow-up to study the maintenance of any observed effect.
    Arm Title
    Second APA program
    Arm Type
    Active Comparator
    Arm Description
    Our study design provides for compensatory participation in the structured program for patients in group 2, following the self-program. From an ethical point of view, this scheme allows all patients included in the structured APA program to benefit. 2nd group: D0: Include S1-S12: APA Autoprogram S13: End of study S14-S25: APA program at IUR Valmante compensatory
    Intervention Type
    Other
    Intervention Name(s)
    Adapted physical activity program
    Intervention Description
    Rehabilitation
    Intervention Type
    Other
    Intervention Name(s)
    Adapted physical activity self-program
    Intervention Description
    Rehabilitation
    Primary Outcome Measure Information:
    Title
    Daily activity measurement
    Description
    Measuring the number of steps per day, collected over the duration of the study, via a Stepwatch device
    Time Frame
    through study completion
    Secondary Outcome Measure Information:
    Title
    the rate physical activities in Written report
    Description
    carried out by the patient, more or less helped by his close entourage, recorded in a notebook given at the beginning of the study
    Time Frame
    through study completion
    Title
    6-minute walk test (6MWT)
    Description
    A test validated in the literature that consists of measuring the greatest distance that a subject can travel on a flat surface (30 meter corridor) in 6 minutes.
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Measurement of heart rate at rest and after 6-minute walk test
    Description
    with a blood pressure cuff
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Measurement of systolic blood pressure at rest and after 6-minute walk test
    Description
    with a blood pressure cuff
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Borg Rating Scale of Exertion
    Description
    test validated in the literature that allows the evaluation of the perception of effort by the patient ; minimum value : 0 = rest : no exertion ; maximum value : 10 = maximal exertion
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Stroke Specific Quality of Life scale (SS-QoL)
    Description
    A test validated in French in the literature that assesses the specific quality of life of stroke patients in 49 items ; minimum value : 1 = Total help/ Couldn't do it at all/ Strongly agree ; maximum value : 5 = No help needed/ No trouble at all/ Strongly disagree
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Berg Balance Scale (BBS)
    Description
    validated scale allowing, by means of 14 instructions, an evaluation of balance, reproducible and sensitive to change ; minimum score : 0-20 = high risk of falling ; maximal score : 56 = no risk of falling
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Activity-specific Balanced Confidence scale (ABC scale)
    Description
    French language validated scale assessing the patient's confidence in his or her balance, using 16 situations where the subject is asked to rate his or her balance on a numerical scale ; minimal rate : 0% = not at all confident ; maximal rate : 100% = completely confident
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)
    Title
    Behavioral regulation in exercise questionnaire
    Description
    scale used in the literature to assess motivation to perform physical activity ; minimal value : 1 = not true at all ; maximal value : 7 = absolutely true
    Time Frame
    at inclusion Day and at the 13th week (and the 26th week for one group only)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Age greater than 18 years Left or right spastic hemiparesis after a first hemorrhagic or ischemic unilateral stroke older than 6 months Walking possible for 6 minutes Exclusion Criteria: Inability to walk without human assistance (with or without technical aids) Cognitive impairment that compromises informed consent, including inability to understand the purpose and terms of the protocol Inability to communicate Presence of an additional neurological disorder Medical conditions that contraindicate physical activity, such as an unbalanced cardiovascular or respiratory condition Concurrent participation in another clinical research project
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Maeva COTINAT
    Phone
    04 91 74 42 00
    Email
    maeva.cotinat@ap-hm.fr
    First Name & Middle Initial & Last Name or Official Title & Degree
    Claire MORANDO
    Phone
    04 91 38 21 83
    Email
    claire.morando@ap-hm.fr

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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