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Not yet recruitingNCT07525154Updated Apr 13, 2026

Development of a Certified Testing Procedure for Hip and Groin Injuries in Athletes

An interventional study of Strength-focused and Flexibility-focused in Hip Injury, sponsored by Charles University, Czech Republic. Not yet recruiting. Open to participants aged 14 Years to 20 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-13.

Sponsored by Charles University, Czech Republic · Not applicable, Interventional, and Screening

Phase
Not applicable
Study type
Interventional
Enrollment
170
Allocation
Randomized
Ages
14 Years to 20 Years
Sex
All
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Study summary

Hip and groin injuries affect approximately 21% of professional athletes annually, causing significant time loss. As roughly 48% of these cases result from non-contact mechanisms, they are potentially preventable through optimized diagnostic screening. Evidence strongly links restricted hip range of motion (ROM) and strength deficits to an increased injury risk. This project aims to (1) develop a rigorously validated diagnostic testing procedure by comparing different joint positions, movement velocities, and muscle contractions to establish a preventive "gold standard" screening battery. dditionally, (2) pilot targeted prevention interventions over a competitive season. Using a crossover design, the research evaluates three protocols: Strength-focused,Flexibility-focused:and control group. (3) Implement of a Centralized Injury Reporting System. Combining comprehensive diagnostic screening with these practical interventions will yield a powerful tool for clinicians and coaches to effectively reduce the incidence and burden of non-contact hip and groin injuries

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Conditions studied

  • Hip Injury

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In context

Hip Injuries

58 studies on the registry are indexed under Hip Injuries; 14 are open to participants now.

This study's planned enrollment of 170 is above the median of 69 across 34 interventional studies indexed under Hip Injuries.

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Lead sponsor

Charles University, Czech Republic is the lead sponsor of 220 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
14 Years to 20 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Male or female competitive team sports.
  • Registered members of participating team sports.
  • Age 14 to 20 years.
  • Participation in regular team training and competition during the study period.
  • Medically cleared for full participation in training and match play at study entry.
  • Willing and able to complete preseason testing and the assigned intervention program.
  • Provided written informed consent. For participants younger than 18 years, parent or legal guardian consent will also be obtained.

Exclusion criteria

Exclusion Criteria:

  • Current hip or groin injury causing time loss or restricting full participation in training or competition at baseline.
  • Lower extremity or lumbar spine injury at baseline that limits safe participation in testing or intervention exercises.
  • Surgery involving the hip, groin, pelvis, lumbar spine, or lower extremity within the previous 6 months.
  • Any neurological, musculoskeletal, cardiovascular, or other medical condition that would contraindicate participation in the intervention or testing procedures.
  • Inability to complete baseline assessments.
  • Planned absence during a substantial part of the preseason intervention period or competitive season.
  • Noncompliance with study procedures or refusal to provide consent.
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Study design

Phase
Not applicable
Primary purpose
Screening
Allocation
Randomized
Intervention model
Crossover assignment
Masking
None (open label)
Enrollment
170 participants (estimated)

Study arms

  • Experimental
    Strength-focused

    Emphasizing specific joint stabilization and eccentric load tolerance, heavily utilizing the Copenhagen Adductor Exercise.

    Other: Strength-focused

  • Experimental
    Flexibility-focused:

    Targeting functional hip ROM through stretching and dynamic mobility under load.

    Other: Flexibility-focused

  • No intervention
    Control

    Maintaining standard club warm-up and training regimens.

Interventions

  • OtherStrength-focused

    Emphasizing specific joint stabilization and eccentric load tolerance, heavily utilizing the Copenhagen Adductor Exercise.

  • OtherFlexibility-focused

    Targeting functional hip ROM through stretching and dynamic mobility under load.

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What researchers measure

Primary outcomes

  1. Hip and Groin Injury Incidence During the Competitive Season

    The number of new hip and groin injuries occurring during the monitored competitive season among athletes participating in the different preseason intervention programs. Injury incidence will be recorded by team medical staff and expressed as the number of injuries per 1000 athlete-exposures.

    Time frame: Through the competitive season, up to 9 months

Secondary outcomes

  1. Hip and Groin Injury Severity

    Severity of hip and groin injuries assessed as the number of days lost from training or competition following injury.

    Time frame: Through the competitive season, up to 9 months

  2. Hip and Groin Injury Burden

    Overall injury burden calculated as the product of injury incidence and injury severity across the study period.

    Time frame: Through the competitive season, up to 9 months

  3. Change in Hip Range of Motion (ROM)

    Passive hip range of motion assessed using standardized clinical ROM testing (Bent Knee Fall-Out test and passive hip flexion/abduction assessments) with a digital inclinometer.

    Time frame: Baseline (Day 1, preseason screening) and 8 weeks (end of preseason intervention)

  4. Functional Lower Limb Performance

    Functional performance of the lower extremity assessed through a standardized testing battery evaluating strength, mobility, and sport-specific functional performance.

    Time frame: Baseline (preseason) and post-intervention (end of preseason)

  5. Hip Adduction and Abduction Strength

    Hip adduction and abduction peak torque measured using isokinetic dynamometry (Humac Norm or Biodex system) during concentric and eccentric contractions at standardized angular velocities (30°/s, 120°/s).

    Time frame: Baseline (Day 1, preseason screening) and 8 weeks (end of preseason intervention)

  6. Isometric Hip Strength

    Isometric hip adduction strength measured using hand-held dynamometry (HHD) squeeze tests and fixed dynamometry systems such as ForceFrame/GroinBar at joint angles of 0°, 25°, and 50° hip abduction.

    Time frame: Baseline (Day 1, preseason screening) and 8 weeks (end of preseason intervention)

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07525154
Lead sponsor
Charles University, Czech Republic
Responsible party
Anna Pisz (PT., Ph.D., Charles University, Czech Republic) — Principal investigator
First posted
Apr 13, 2026
Start date
Jan 1, 2027 (estimated)
Primary completion
Dec 31, 2031 (estimated)
Completion
Dec 31, 2031 (estimated)
Last update
Apr 13, 2026

Study contacts

Anna Pisz, PT, PhD
Contact
anna.pisz@ftvs.cuni.cz
+420703952913

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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