- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07336524
Ankle Isometric Strength and Proprioception in Young Ice Hockey Players (ANKLE-ICE)
December 30, 2025 updated by: Emine Merve Ersever
Comparison of Ankle Isometric Strength and Proprioception Between 9-10-Year-Old Junior Ice Hockey Players and Age-Matched Controls
This observational cross-sectional study aims to profile ankle isometric strength and proprioception in 9-10-year-old junior ice hockey players and to compare these outcomes and limb symmetry indices with age-matched non-athlete children.
Ankle isometric muscle strength is assessed using a handheld dynamometer, and ankle proprioception is evaluated using a digital inclinometer.
Measurements are performed bilaterally for dominant and non-dominant limbs.
Group comparisons and limb symmetry analyses are conducted to identify potential neuromuscular differences related to sports participation.
Study Overview
Status
Not yet recruiting
Study Type
Observational
Enrollment (Estimated)
70
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
The study includes 70 healthy children aged 9-10 years, comprising junior ice hockey players and age-matched non-athlete controls.
Description
Inclusion Criteria:
- Children aged 9 to 10 years.
- For the ice hockey group: regular participation in organized junior ice hockey training.
- For the control group: no participation in organized sports or structured athletic training.
- Ability to understand and follow test instructions.
- Written informed consent obtained from parents or legal guardians
Exclusion Criteria:
- History of lower extremity injury within the past 6 months.
- Previous ankle or lower limb surgery.
- Presence of neurological, musculoskeletal, or balance disorders that could affect ankle strength or proprioception.
- Current pain or injury affecting lower extremity function.
- Any medical condition that would limit safe participation in the assessments.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
|
Junior Ice Hockey Players
Children aged 9-10 years who participate in organized junior ice hockey training on a regular basis
|
|
Non-Athlete Children
Age-matched children aged 9-10 years who do not participate in organized sports or structured athletic training.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ankle Isometric Strength
Time Frame: Single assessment session
|
Ankle isometric muscle strength of the dominant and non-dominant limbs measured using a hand-held dynamometer (Lafayette Manual Muscle Testing System).
Peak force values are recorded for dorsiflexion, plantar flexion, inversion, and eversion.
|
Single assessment session
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ankle Proprioception
Time Frame: Single assessment session
|
Ankle joint proprioception assessed bilaterally for the dominant and non-dominant limbs using a joint position sense test with a digital inclinometer.
Proprioceptive accuracy is expressed as absolute error in degrees between the target and reproduced ankle joint position.
|
Single assessment session
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
December 15, 2025
Primary Completion (Estimated)
January 15, 2026
Study Completion (Estimated)
March 15, 2026
Study Registration Dates
First Submitted
December 16, 2025
First Submitted That Met QC Criteria
December 30, 2025
First Posted (Actual)
January 13, 2026
Study Record Updates
Last Update Posted (Actual)
January 13, 2026
Last Update Submitted That Met QC Criteria
December 30, 2025
Last Verified
December 1, 2025
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- E-18/231
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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