Effects of the Copenhagen Plank on Hip Adductor Strength and Countermovement Jump Height in Female Soccer Players: A Randomized Controlled Trial

July 4, 2026 updated by: Javier Reina Abellan; PhD, Universidad de Murcia
evaluate the effects of a 4-week Copenhagen Plank protocol on hip adductor strength and countermovement jump (CMJ) height in female soccer players and to determine whether adaptations were maintained during a 4-week follow-up.

Study Overview

Study Type

Interventional

Enrollment (Actual)

25

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Murcia
      • Murcia, Murcia, Spain
        • MURCIA

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

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • All players trained at least twice weekly. The Copenhagen Plank intervention was supervised by a strength and conditioning coach with ≥10 years of experience in elite or sub-elite soccer. Inclusion criteria were being an active federated player, age between 18 and 35 years, and absence of lower limb injuries in the 6 months prior to the study

Exclusion Criteria:

  • 2 were excluded for recent injuries and one player left the team before the data collection began.

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

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: CONTROL GROUP
Experimental: experimental group
EXPERIMENTAL GROUP
Participants performed a progressive Copenhagen Plank exercise program twice weekly for 4 weeks in addition to their regular soccer training. The program started with 2 sets of 8-10 repetitions per side and progressed to 3 sets of 12-15 repetitions per side during the final week. All sessions were supervised by a strength and conditioning coach.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Isometric Hip Adductor Strength
Time Frame: Baseline, 4 weeks (post-intervention), and 8 weeks (4-week follow-up)
Isometric hip adductor strength of the dominant and non-dominant limbs was assessed using a Lafayette handheld dynamometer during the long-lever squeeze test. The highest value of three maximal voluntary isometric contractions was recorded and expressed in Newtons (N).
Baseline, 4 weeks (post-intervention), and 8 weeks (4-week follow-up)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Countermovement Jump Height
Time Frame: Baseline, 4 weeks (post-intervention), and 8 weeks (4-week follow-up)
Countermovement jump height was measured using a Chronojump contact platform. Participants performed three jumps with their hands on their hips, and the highest jump height (cm) was recorded.
Baseline, 4 weeks (post-intervention), and 8 weeks (4-week follow-up)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 (Actual)

November 2, 2022

Primary Completion (Actual)

March 29, 2023

Study Completion (Actual)

May 23, 2023

Study Registration Dates

First Submitted

July 4, 2026

First Submitted That Met QC Criteria

July 4, 2026

First Posted (Actual)

July 10, 2026

Study Record Updates

Last Update Posted (Actual)

July 10, 2026

Last Update Submitted That Met QC Criteria

July 4, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • CE012302 (Registry Identifier: Javier Reina-Abellán , Luis Blanco-López , Rocío Martínez-Fernández , Cinta Gómez-Tomás)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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