The Micheli Functional Scale's Validity and Reliability

Sponsor
Hacettepe University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06001229
Collaborator
(none)
80
10.2

Study Details

Study Description

Brief Summary

The purpose of this study is to assess the reliability and validity of the "Micheli Functional Scale" in the Turkish context.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The study will include a minimum of 80 individuals who are 16 years old or above, have been engaged in the same sports activity for at least two years, participate in physically demanding activities for at least three days a week, and possess the ability to read and write Turkish. Before participating in the study, athletes will be required to sign an informed consent form. Their demographic information will then be recorded.Before conducting the test, we will gather information about the athletes' history of low back pain using the extended Nordic musculoskeletal questionnaire. We will also use this questionnaire to identify any other musculoskeletal issues that the person may have.Two Turkish translators, fluent in English, will independently translate the original Micheli Functional Scale into Turkish. They will then discuss their translations and create a common one. The resulting translation will be translated back into English by two native English speakers who are also proficient in Turkish. These translations will be reviewed and combined into a single version. A Turkish scientist will evaluate the questionnaire for its suitability in the Turkish language. The final version will be tested on a small pilot group to determine its comprehensibility. After this, the questionnaire will be administered to the entire study group. To assess the validity of the Micheli Functional Scale, we will use the Oswestry Functional Questionnaire and the Ronald Morris Disability Questionnaire. One week after the test, we will repeat these surveys.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    80 participants
    Observational Model:
    Other
    Time Perspective:
    Other
    Official Title:
    The Micheli Functional Scale's Validity and Reliability in Turkish Sport Groups
    Anticipated Study Start Date :
    Aug 18, 2023
    Anticipated Primary Completion Date :
    Jun 22, 2024
    Anticipated Study Completion Date :
    Jun 22, 2024

    Outcome Measures

    Primary Outcome Measures

    1. Micheli Functional Scale [baseline and 1 week later]

      Evaluates the function linked to low back pain in athletes.

    2. Oswestry Disability Index [baseline and 1 week later]

      Evaluate disability due to low back pain. the index measures perceived low back pain related dysfunction. Whether the total score increaeses, the dyscfunction increases.

    3. Roland morris disability questionnaire [baseline and 1 week later]

      It is a questionnaire used to evaluate the disability level of individuals with low back pain. This questionnaire, consisting of 24 items, questions the person's social life, walking, sitting, standing, getting up from a chair, climbing stairs, dressing, personal care, pain, appetite, sleep, and psychological impact. The person answers the questions with yes and no. Yes is scored as 1 point and no as 0 points. The maximum score is "24" and the minimum score is "0". As the total score increases, the level of physical exposure also increases.

    Secondary Outcome Measures

    1. The musculoskeletal system problem [baseline]

      Nordic Musculoskeletal System Questionnaire

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    16 Years to 25 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 16 years old and over

    • Having been doing the same sport for at least 2 years,

    • Participating in sports activities or activities that require a high level of effort at least 3 days a week,

    • Able to read and write Turkish

    Exclusion Criteria:
    • Has a cognitive problem that prevents him from understanding and answering the questions or is taking a drug that may cause them,

    • Having a history of orthopedic or neurological injury or pain at a level that may prevent training or competition during the evaluation,

    • History of spine/lower and upper extremity surgery,

    • Structural deformities such as scoliosis and kyphosis,

    • Those with trap neuropathy will be excluded from the study.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Hacettepe University

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Aynur Demirel, Associate Professor, Hacettepe University
    ClinicalTrials.gov Identifier:
    NCT06001229
    Other Study ID Numbers:
    • GO 22/540
    First Posted:
    Aug 21, 2023
    Last Update Posted:
    Aug 21, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 21, 2023