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NCT Number: NCT06733116

Standardizing Reporting Practices for Isokinetic Testing: a Delphi Study

Isokinetic testing plays a crucial role in research and clinical practice, particularly for evaluating muscle strength, functional performance, and imbalances between muscle groups in fields such as rehabilitation, sports medicine, and orthopedics. Despite its widespread use, there is no international consensus on how to standardize protocols or report results, leading to significant variability in methodologies, measurement parameters, and data presentation.

This Delphi method study aims to develop a consensus framework for standardizing the reporting of isokinetic testing data, ensuring consistency and comparability in research and clinical practices.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

Isokinetic tests are widely used in research and clinical practice to evaluate muscle strength, imbalances between muscle groups, and functional performance. These assessments are particularly important in rehabilitation, sports medicine, and orthopedics. However, the diversity in testing protocols, measured parameters, and reporting methods creates significant challenges for the comparability and interpretation of results.

Currently, there is no international consensus on how to report isokinetic test results. Scientific publications and clinical reports vary greatly in methodologies, units of measurement, and presentation of findings. Additionally, there is considerable heterogeneity in how results are presented, particularly regarding essential elements that ensure methodological reproducibility. This variability complicates the synthesis of data across studies and limits their practical application. As a result, healthcare professionals and researchers struggle to compare results, replicate studies, or effectively use the data in clinical decision-making.

The need to standardize reporting practices for isokinetic tests is therefore clear. A standardized framework would harmonize reporting, facilitate comparisons between studies, support the evaluation of therapeutic interventions, and improve the monitoring of patients or athletes over time. It would also enhance transparency and scientific rigor, which are critical for advancing knowledge and improving care.

The Delphi method, used in this study, is particularly suited to addressing this issue. It relies on an iterative process to gather the opinions of a panel of experts and establish a consensus on specific recommendations. By involving experts from various fields (physicians, physiotherapists, kinesiologists, and sport physiologists), this method ensures that the recommendations reflect a broad and balanced perspective. It also helps structure and prioritize key points, identifying essential elements for a standardized report.

The results of this study are expected to have several significant outcomes. First, they will provide a clear framework for standardizing the reporting of isokinetic tests, improving the quality and utility of the data reported. Second, this framework could be adopted internationally, fostering better collaboration between researchers and clinicians. Finally, it could serve as a foundation for developing official guidelines or recommendations, enhancing the validity and impact of isokinetic testing in clinical and scientific practices.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Demonstrated knowledge or experience in isokinetic testing, such as research, clinical practice, or equipment design.
  • Clinicians, researchers, educators, or professionals with relevant expertise in rehabilitation, sports medicine, biomechanics, or related fields.
  • At least 5 peer-reviewed publication (first author) or equivalent contribution in the field of isokinetic testing or related domains.
  • Minimum of 5 years of professional experience in a relevant field.
  • Agreement to participate in all Delphi rounds and provide informed consent.
  • Ability to communicate and provide responses in the language used for the study (English).

Exclusion criteria

  • Professionals with conflicts of interest that could bias their contributions, such as direct financial ties to specific isokinetic testing equipment manufacturers.
  • Inability or unwillingness to commit to the iterative Delphi process, including providing timely responses to questionnaires.
  • Accidental inclusion of an expert already represented in another capacity within the study (e.g., as a member of the organizing committee).

Treatment and study plan

Delphi method survey

Other

This intervention involves a Delphi method study, where a panel of experts in isokinetic testing will collaborate to reach a consensus on best practices for standardizing the reporting of isokinetic test data. Unlike other clinical studies, this intervention focuses on gathering expert opinions iteratively to establish a unified framework for data reporting, without direct clinical or experimental treatment. The process includes multiple rounds of feedback, refining key elements related to testing protocols, measurement parameters, and result presentation, ensuring broad expertise from various fields such as medicine, rehabilitation, and biomechanics.

Primary outcomes

  1. Consensus on Key Elements for Standardized Reporting of Isokinetic Testing

    Time frame: At the completion of the final Delphi round (approximately 6 months).

    The proportion of agreement among experts on the key elements to include in a standardized framework for reporting isokinetic testing data, as determined by the final round of the Delphi process. Agreement will be defined as at least 80% agreement (4 or 5 on a 5 -level Likert scale, minimum=1 maximum=5, 5 corresponding to 'strongly agree')

Secondary outcomes

  1. Open Survey to Inform Delphi Rounds

    Time frame: At the end of the first Delphi round (approximately 2 month)

    The identification and categorization of items related to isokinetic testing, informed by an initial literature review and expert input during Round 1 of the Delphi process.

  2. Prioritization of Reporting Items

    Time frame: During intermediate Delphi rounds (approximately 3-4 months).

    Ranking of reporting items by importance ("1 = optional", "2 = recommended", "3 = essential"), with 'essential' indicating that the item is mandatory, based on iterative feedback from Delphi panelists.

  3. Years of Professional Practice

    Time frame: At the beginning of the Delphi process (baseline).

    Average and range of years of professional experience in fields related to isokinetic testing (e.g., sports medicine, rehabilitation, research).

  4. Academic Contributions

    Time frame: At the beginning of the Delphi process (baseline).

    Number of peer-reviewed publications or other academic contributions related to isokinetic testing or related fields, self-reported by the participants.

  5. Geographic Distribution of Expert Panel Participants

    Time frame: At the beginning of the Delphi process (baseline).

    Distribution of experts by geographic region (e.g., continents, countries) to evaluate the representativeness of the panel.

  6. Expert Panel Composition - gender

    Time frame: At the beginning of the Delphi process (baseline).

    Analysis of gender distribution within the expert panel

  7. Expert Panel Composition - country

    Time frame: At the beginning of the Delphi process (baseline).

    Analysis of the country of residence distribution within the expert panel

  8. Expert Panel Composition - job

    Time frame: At the beginning of the Delphi process (baseline).

    Analysis of the type of job distribution within the expert panel

Study contacts

Contact information is provided by the study sponsor or research team.

Joffrey DRIGNY, MD PhD

CONTACT

[email protected]

+33 0231064892

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Collaborators

  • INSERM UMR U1075 Comète GIP Cyceron, unicaen, Caen Normandie

Registry information

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Dec 13, 2024
Registry last updated
Dec 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.