AzTrials
AzTrials

Groin InjuryNCT06104722

Comparison of the Effect of Copenhagen Adduction Exercises Performed at Different Load-intensity

A study testing High-intensity Copenhagen adduction exercise and Low-intensity Copenhagen adduction exercise in people with Groin Injury, run by Hacettepe University at 1 site in Turkey (Türkiye).

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
Search all trials

Trial summary

The aim of our study is to compare the effects of the Copenhagen adduction exercise, performed at different loading intensities, on hip muscle strength development, performance, flexibility, and delayed onset muscle soreness. The study will include active taekwondo athletes between the ages of 12-18. Read more about this study

Who is it for?
Ages 12 to 18 yearsHealthy volunteers can take part
Conditions the study is for
Groin Injury
What is being tested?
High-intensity Copenhagen adduction exercise and Low-intensity Copenhagen adduction exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
1 siteTurkey (Türkiye)
Study dates
15 Jan 2024to 15 Jul 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 to 18 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • Being between the ages of 12-18
  • Having a minimum of 3 years of experience as a taekwondo athlete
  • Not having experienced any back, hip, or groin injuries in the last 12 months
  • Participating in training sessions at least 3 days a week
  • Being available to attend exercise training for 8 weeks

Who cannot join

  • Having had a lower extremity orthopedic injury within the last 3 months
  • Having an injury related to the hip and groin region
  • Reporting a pain level of 4 or higher on the visual pain scale during the adductor squeeze test and palpation of the adductor muscles

Trial locations and contacts

1 site in 1 country.

Ezgi Unuvar-Yuksel contact

+905078337676

unuvarezgi@gmail.com

Özlem Ulger, proffesor contact

+903123051576

ozlemulger@yahoo.com

Turkey (Türkiye)1 site, 1 recruiting
  • Hacettepe University

    Ankara, Altındag, 06100

    Ezgi Unüvar, 05078337676, unuvarezgi@gmail.com

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Comparison of the Effects of Copenhagen Adduction Exercise Performed at Different Loading Intensities on Hip Muscle Strength Development, Delayed Muscle Soreness, and Lower Extremity Physical Fitness Parameters

The aim of our study is to compare the effects of the Copenhagen adduction exercise, performed at different loading intensities, on hip muscle strength development, performance, flexibility, and delayed onset muscle soreness. The study will include active taekwondo athletes between the ages of 12-18. Athletes will be randomly divided into two groups: a low-intensity Copenhagen Adduction exercise group and a high-intensity Copenhagen Adduction exercise group. Athletes in both the low-intensity and high-intensity exercise groups will perform the exercise for 8 weeks in addition to their regular training program. At the beginning of the study and at the 4th, 8th, and 16th weeks, assessments will be conducted for hip abductor and adductor eccentric and isometric muscle strength, flexibility of the hip adductors, level of delayed muscle soreness, single-leg jump test, and timed lateral hop tests. The outcome of our study will determine how much improvement is achieved in hip muscle strength and lower extremity physical fitness parameters during and after the application of the Copenhagen adduction exercise at different loading intensities.

Read the detailed description

The study is a single-blind randomized controlled trial including male and female adolescent taekwondo athletes (12-18 years). Evaluators will be blinded to which group are assessing.

Participants will be recruited from the local sports clubs. Club coaches will be asked to invite club players. Players interested in participating in the study will be asked to attend a meeting where the study will be explained to them. Those who were interested will then be assessed for inclusion and exclusion criteria.

Interventions:

Sports clubs are allocated to the high-intensity Copenhagen adductor exercise group (HCAE) or the low-intensity Copenhagen adduction exercise group (LCAE). Athletes in both the low-intensity and high-intensity exercise groups will perform the exercise for 8 weeks. Athletes in the HCAE group will perform the classic Copenhagen adduction exercise protocol and at LCAE group will perform the modified Copenhagen adduction exercise protocol.

Testing procedure:

The following tests will be performed before the exercise and 4th - 8th - 16th weeks after the beginning of the exercise.

The isometric and eccentric strength of the hip adductors and abductors Hip adduction flexibility Single-leg hop test Side hop test

A 10-point visual analog scale will be used to record the level of muscle soreness and rate of perceived exertion experienced after each training session.

Conditions
Groin Injury
Being tested
High-intensity Copenhagen adduction exercise, Low-intensity Copenhagen adduction exercise

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • High-intensity Copenhagen adduction exerciseOther

    Copenhagen adduction exercise is an eccentric strengthening protocol of hip adductors and suitable for groin injury prevention and rehabilitation.

  • Low-intensity Copenhagen adduction exerciseOther

    Copenhagen adduction exercise is an eccentric strengthening protocol of hip adductors and suitable for groin injury prevention and rehabilitation.

Study groups in NCT06104722
Study groupRoleWhat they receive
high intensity copenhagen adduction exercise groupExperimentalAthletes in the high-intensity copenhagen adduction exercise group will perform classic copenhagen adduction exercise protocol.
Receives: Other: High-intensity Copenhagen adduction exercise
low intensity copenhagen adduction exercise groupExperimentalAthletes in the low-intensity copenhagen adduction exercise group will perform a modified copenhagen adduction exercise protocol.
Receives: Other: Low-intensity Copenhagen adduction exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. hip muscle strength

    isometric and eccentric hip adductor and abductor muscle strength will assess with a hand-held dynamometer.

    Measured: beginning and 4th-8th-16th weeks after beginning

Secondary outcomes (4)
  1. lower extremity performance

    single leg hop test and side hop test

    Measured: beginning and 4th-8th-16th weeks after beginning

  2. hip adduction flexibility

    hip adduction range of motion will assess with a goniometer.

    Measured: beginning and 4th-8th-16th weeks after beginning

  3. delayed onset muscle soreness

    delayed onset muscle soreness will assessed with visual analog scale.

    Measured: immediately after each exercise session, through 8 weeks

  4. rate of perceived exertion

    rate of perceived exertion will assessed with BORG CR10 scale(Borg Rating Of Perceived Exertion).

    Measured: immediately after each exercise session, through 8 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Oct 2023
  2. Study start15 Jan 2024
  3. Primary completion15 Jun 2024 (estimated)
  4. Study completion15 Jul 2024 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Screening
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06104722
Sponsor's protocol ID
copenhagentkd2023
Status last verified
Jun 2024
First submitted
12 Oct 2023
Last updated
5 Jun 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Publications

  • Unuvar-Yuksel E, Bozgeyik-Bagdatli S, Bazancir-Apaydin Z, Guney-Deniz H. Early strength gains in eccentric hip adduction and adduction-to-abduction ratio following an 8-week Copenhagen Adduction Exercise in elite adolescent taekwondo athletes. J Bodyw Mov Ther. 2025 Dec;45:304-310. doi: 10.1016/j.jbmt.2025.09.008. Epub 2025 Sep 5.

    PubMed 41316591

Questions about this trial

What is this clinical trial studying?

A study testing High-intensity Copenhagen adduction exercise and Low-intensity Copenhagen adduction exercise in people with Groin Injury, run by Hacettepe University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 5 Jun 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Ezgi Unuvar-Yuksel (+905078337676, unuvarezgi@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

hip muscle strength (time frame: beginning and 4th-8th-16th weeks after beginning). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06104722, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Jun 2024.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in