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NCT Number: NCT06955026

Effect of the Hockey Slideboard Training Combined With Blood Flow Restriction (BFR) in the Rehabilitation Following Anterior Cruciate Ligament Surgical Reconstruction (ACL-R)

ACL injuries represent a major health and economic burden. The overall incidence of ACL injuries has increased and is likely to continue to increase, in part due to increased sports participation.

In the acute post-surgical phase there is a period of physiologic recovery from the surgical injury and subsequent relative muscle disuse that is associated with atrophy loss of strength and anterior knee pain. Therefore, improvement of muscle function is a priority in the rehabilitation and reathletization process.

To achieve significant muscle hypertrophy as well as a possible subsequent increase in strength, it is widely accepted that resistance exercises with relevant load (~70% of the one repetition maximum - 1RM) are necessary; however, in patients undergoing anterior cruciate ligament reconstruction (ACL-R), exercises with high loads are considered unsafe in the early stages and could increase the risk of re-injury.

BFR training is an established muscle training and rehabilitation technique in which the blood supply to and from the muscles involved in the exercise is restricted using an external device.

Although the physiological mechanisms related to this intervention are not yet well understood, it is thought that in BFR training, despite the low level of mechanical tension, the main driver of myocellular hypertrophy could be metabolic stress that is realized by local accumulation of metabolites. Thus, it seems that hypertrophic adaptations can be induced with much lower exercise intensities using BFR. In fact, when combined with low-load resistance training (e.g., 20% 1RM), training with BFR has shown positive results in increasing muscle volume and strength after ACL-R in complete safety comparable to standard training without BFR.

It has also already been demonstrated how incorporating the use of the hockey slideboard into the rehabilitation procedure following ACL-R gives benefits in terms of strength recovery of the extensor muscles of the operated limb with the same safety profiles as standard rehabilitation.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Spital Municipal Odorheiu Secuiesc

Odorheiu Secuiesc, Romania, 535600

Location status: Recruiting

Location contact

Claudia I Nedelcu, Master, BSc

CONTACT

[email protected]

0040728258216

Claudia I Nedelcu, Master, BSc

PRINCIPAL_INVESTIGATOR

Toma Vasilescu, Master, BSc

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • having undergone ACL-R following a unilateral rupture, with reconstructive surgical technique by bone-patellar tendon-bone autograft (BPTB) or semitendinosus-gracilis autograft (STG)
  • ACL-R including associated meniscal lesions treated with selective meniscectomy and/or non-complex meniscal suture

Exclusion criteria

  • not having undergone ACL-R following a unilateral rupture, with reconstructive surgical technique by bone-patellar tendon-bone autograft (BPTB) or semitendinosus-gracilis autograft (STG)

Treatment and study plan

Hockey slideboard combined with BFR training

Other

Hockey slideboard combined with BFR training

Hockey slideboard

Other

Hockey slideboard

Primary outcomes

  1. Adductor muscles maximal voluntary isometric contraction (MVIC)

    Time frame: Before the study intervention (T0) and after the study intervention lasting for four weeks (T1)

    Adductor muscles' maximal voluntary isometric contraction (MVIC) measured via hand-held dynamometer test in a supine position

Secondary outcomes

  1. Abductor muscles maximal voluntary isometric contraction (MVIC)

    Time frame: Before the study intervention (T0) and after the study intervention lasting for four weeks (T1)

    Abductor muscles' maximal voluntary isometric contraction (MVIC) measured via hand-held dynamometer test in a supine position

  2. Adductor/abductor isometric strength (MVIC) ratio

    Time frame: Before the study intervention (T0) and after the study intervention lasting for four weeks (T1)

    Adductor and abductor muscles' maximal voluntary isometric (MVIC) strength ratio measured via hand-held dynamometer test in a supine position

  3. Y-balance test (YBT) composite score

    Time frame: Before the study intervention (T0) and after the study intervention lasting for four weeks (T1)

    The YBT assessment demands that the athlete maintain balance on one leg while extending the opposite leg as far as feasible in three different directions: anterior, posterolateral, and posteromedial. The YBT composite score is calculated by summing the three reach distances and normalizing them to the lower limb length.

  4. Triple hop test for distance

    Time frame: After the study intervention lasting for four weeks (T1)

    Triple hop test executed, calculating the maximum reached distance and comparing the healthy limb result with the involved leg.

  5. Single hop test for distance

    Time frame: After the study intervention lasting for four weeks (T1)

    Single hop test executed, calculating the maximum reached distance and comparing the healthy limb result with the involved leg.

  6. Side hop test

    Time frame: After the study intervention lasting for four weeks (T1)

    The participant is required to hop from side to side on one limb outside two parallel strips of tape 40 cm apart, and instructed to hop as many hops as possible for 30 seconds.

Study contacts

Contact information is provided by the study sponsor or research team.

Claudia I Nedelcu, Master, BSc

CONTACT

[email protected]

0040728258216

Sebastiano Nutarelli, Master, BSc

CONTACT

[email protected]

0041779501650

Sponsors and collaborators

Lead sponsor

Spitalul Municipal Odorheiu Secuiesc

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 2, 2025
Registry last updated
May 2, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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