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The Effects of Trunk Impairment on Fatigue and Balance

Primary Purpose

Cerebral Palsy

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Trunk Impairment Scale (TIS), PedsQLTM Multidimensional Fatigue Scale (PedsQL-MFS), Pediatric Balance Scale (PBS)
Sponsored by
Suleyman Demirel University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Cerebral Palsy

Eligibility Criteria

2 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

aged between 2-18 years old; (2) had a form of CP; (3) had the cognitive competence to participate to the all assessments.

Exclusion Criteria:

The sufferers who had an additional neurological or musculoskeletal disability, unstable medical conditions, any recent medical intervention (such as tendon lengthening surgery or botulinum toxin injection…) were excluded

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Placebo Comparator

    Active Comparator

    Arm Label

    Control

    Study

    Arm Description

    Outcomes

    Primary Outcome Measures

    Trunk Impairment Scale (TIS)
    PedsQLTM Multidimensional Fatigue Scale (PedsQL-MFS)
    Pediatric Balance Scale (PBS)

    Secondary Outcome Measures

    Full Information

    First Posted
    September 13, 2021
    Last Updated
    September 13, 2021
    Sponsor
    Suleyman Demirel University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05050422
    Brief Title
    The Effects of Trunk Impairment on Fatigue and Balance
    Official Title
    The Effects of Trunk Impairment on Fatigue and Balance in Children With CP
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    September 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 13, 2021 (Anticipated)
    Primary Completion Date
    October 13, 2021 (Anticipated)
    Study Completion Date
    October 13, 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Suleyman Demirel University

    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
    Fatigue is a common symptom associated with cerebral palsy (CP); it has been estimated that up to 40% of adolescents with CP experience fatigue that impacts their quality of life and daily activities. Although fatigue was stated as the primary symptom, a limited number of studies were found on secondary motor and nonmotor symptoms related to trunk control in children when the literature was examined.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Screening
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Non-Randomized
    Enrollment
    64 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Control
    Arm Type
    Placebo Comparator
    Arm Title
    Study
    Arm Type
    Active Comparator
    Intervention Type
    Diagnostic Test
    Intervention Name(s)
    Trunk Impairment Scale (TIS), PedsQLTM Multidimensional Fatigue Scale (PedsQL-MFS), Pediatric Balance Scale (PBS)
    Intervention Description
    control/study group
    Primary Outcome Measure Information:
    Title
    Trunk Impairment Scale (TIS)
    Time Frame
    1 month
    Title
    PedsQLTM Multidimensional Fatigue Scale (PedsQL-MFS)
    Time Frame
    1 month
    Title
    Pediatric Balance Scale (PBS)
    Time Frame
    1 month

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    2 Years
    Maximum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: aged between 2-18 years old; (2) had a form of CP; (3) had the cognitive competence to participate to the all assessments. Exclusion Criteria: The sufferers who had an additional neurological or musculoskeletal disability, unstable medical conditions, any recent medical intervention (such as tendon lengthening surgery or botulinum toxin injection…) were excluded

    12. IPD Sharing Statement

    Plan to Share IPD
    Undecided

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