NCT07822568

Brief Summary

This randomized controlled trial compared two exercise approaches for strengthening the hip adductor muscles in healthy, recreationally active adults. Participants were assigned to one of three groups: training using a custom isokinetic device, training using the Copenhagen adduction exercise, or a control group that did not perform the specific hip adductor training. The intervention lasted 8 weeks. The device-based program used controlled eccentric muscle actions, in which the hip adductors produce force while being lengthened, whereas the Copenhagen adduction exercise involved a commonly used body-weight strengthening exercise. The purpose of the study was to determine how these two types of hip adductor training affect muscle strength and other physical characteristics that may be relevant to performance and the prevention of groin and hip adductor injuries. The main research question was whether training with the isokinetic device produces different and potentially greater adaptations than the Copenhagen adduction exercise and no specific training. The study hypothesis was that device-based eccentric training would lead to greater improvements in hip adductor strength and related functional and muscle characteristics than copenhagen adduction exercise training, while the control group would show little or no change.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
55

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Sep 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 30, 2024

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 19, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 19, 2026

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 10, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

September 16, 2026

Completed
Last Updated

September 21, 2026

Status Verified

September 1, 2026

Enrollment Period

1.6 years

First QC Date

September 10, 2026

Last Update Submit

September 16, 2026

Conditions

Outcome Measures

Primary Outcomes (3)

  • Eccentric adductor peak torque

    Eccentric hip adductor peak torque of the dominant leg measured using an isokinetic dynamometer (Humac Norm) at an angular velocity of 30°/s

    Baseline and during Week 9, following completion of the 8-week intervention

  • Eccentric work

    Work during eccentric hip adductor contraction of the dominant leg measured using an isokinetic dynamometer (Humac Norm) at an angular velocity of 30°/s

    Baseline and during Week 9, following completion of the 8-week intervention

  • Adductor longus muscle thickness

    Adductor longus muscle thickness measured using ultrasound imaging.

    Baseline and during Week 9, following completion of the 8-week intervention

Secondary Outcomes (8)

  • Angle at peak torque during eccentric contraction

    Baseline and during Week 9, following completion of the 8-week intervention

  • Concentric adductor peak torque

    Baseline and during Week 9, following completion of the 8-week intervention

  • Concentric abductor peak torque

    Baseline and during Week 9, following completion of the 8-week intervention

  • Hip Adduction:abduction strength ratio

    Baseline and during Week 9, following completion of the 8-week intervention

  • Lateral shuffle test

    Baseline and during Week 9, following completion of the 8-week intervention

  • +3 more secondary outcomes

Study Arms (3)

Isokinetic device-based training

EXPERIMENTAL

Participants completed an 8-week hip adductor training program using an isokinetic device. Training consisted of controlled eccentric hip adduction exercise, in which the hip adductor muscles produced force while being lengthened. Training was performed twice per week with progressive training volume.

Other: Isokinetic device-based hip adductor training

Copenhagen adduction exercise training

EXPERIMENTAL

Participants completed an 8-week hip adductor strengthening program using the Copenhagen adduction exercise. Training was performed twice per week, with the number of sets and repetitions progressively increased during the intervention.

Other: Copenhagen adduction exercise training

Control

NO INTERVENTION

Participants did not perform either of the study-specific hip adductor training programs during the 8-week intervention period.

Interventions

An 8-week, twice-weekly hip adductor training program performed using an isokinetic device. The exercise involved controlled eccentric contractions of the hip adductors. The device moved the lower limbs into hip abduction at a controlled angular velocity while participants resisted the movement with the hip adductor muscles. Training volume was progressively increased over the intervention.

Isokinetic device-based training

An 8-week, twice-weekly hip adductor strengthening program using the Copenhagen adduction exercise. Participants performed the exercise with an emphasis on the eccentric phase, and training volume was progressively increased.

Copenhagen adduction exercise training

Eligibility Criteria

Age18 Years+
Sexmale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Healthy and free from musculoskeletal injury at the time of enrollment;
  • Recreationally active males;
  • Able to successfully complete 5 repetitions of the Copenhagen adduction exercise.

You may not qualify if:

  • Serious injury to nervous, muscular, skeletal, or connective tissue involving the back, hip, or lower extremities within the previous 12 months
  • Inability to perform the Copenhagen adduction exercise

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Fakulteta za vede o zdravju

Izola, 6310, Slovenia

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Porf. Dr.

Study Record Dates

First Submitted

September 10, 2026

First Posted

September 16, 2026

Study Start

September 30, 2024

Primary Completion

May 19, 2026

Study Completion

May 19, 2026

Last Updated

September 21, 2026

Record last verified: 2026-09

Data Sharing

IPD Sharing
Will share

Locations