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Mulligan Techniques for Gait and Pelvic Motion in Short Hamstrings

25 septembre 2026 mis à jour par: Gamze COBANOGLU, Gazi University

The Effect of Two Different Mulligan Techniques on Spatiotemporal Parameters and Pelvic Oscillation in Individuals With Hamstring Tightness: A Randomized Controlled Trial

Various stretching methods have been developed to reduce hamstring tightness and improve flexibility. Static stretching is one of the safest and most common methods used to increase muscle length; however, its effect is temporary and diminishes rapidly. Additionally, such conventional methods can be uncomfortable and require longer periods to yield visible results. Unlike other mobilization procedures, the Mulligan concept is performed while patients execute a resisted muscle contraction or move actively or passively. Distinct from many other manual therapy approaches, this technique is applied within a symptom-free range of motion, which likely enhances its safety. Traction Straight Leg Raise (TSLR) and Bent Leg Raise (BLR) techniques are specific interventions defined by Mulligan. There are limited studies in the literature investigating the effects of these two techniques on hamstring flexibility. However, no study has compared these two techniques in terms of spatiotemporal gait parameters and pelvic oscillations. Therefore, the purpose of this study is to compare the effects of BLR and TSLR techniques applied to individuals with hamstring tightness on hamstring flexibility, spatiotemporal parameters of gait, and pelvic oscillations.

Aperçu de l'étude

Description détaillée

Flexibility holds a significant place among health-related physical fitness parameters and is defined as the normal range of motion achievable by a joint and/or joint complexes. Muscle flexibility is crucial for maintaining optimal muscle functionality and proper biomechanics. Limited flexibility leads to various musculoskeletal symptoms, postural deformities, and gait limitations. Reduced flexibility is commonly observed in fast-twitch and biarticular muscles, with the hamstring muscles being a prime example. The length of the hamstring muscles plays an essential role in human movement, including gait. Hamstring tightness reduces the ability to absorb shocks applied to the lower extremity and knee extension during walking, thereby decreasing step length. Individuals with hamstring tightness do not exhibit a normal gait pattern, particularly during the mid-swing and terminal swing phases. Furthermore, hamstring tightness results in reduced pelvic mobility. Decreased hamstring flexibility is a frequently observed finding in numerous musculoskeletal problems of the knee, hip, and lumbar regions. By disrupting the muscle length-tension relationship in the posterior kinetic chain, it has been specifically associated with clinical conditions such as low back pain, patellofemoral pain syndrome, and posterior pelvic tilt. Therefore, addressing this tightness stands out as a major goal in rehabilitation and exercise programs. Traction Straight Leg Raise (TSLR) and Bent Leg Raise (BLR) techniques are specific interventions. Only a limited number of studies have compared these two methods in individuals with hamstring tightness. Kapadia and Meshram reported that both of Mulligan's TSLR and BLR techniques are effective in improving hamstring muscle flexibility in healthy individuals; however, they noted that the TSLR technique was superior in enhancing flexibility. Priyanka et al. applied TSLR and BLR interventions to collegiate cricket players for a duration of two weeks and concluded that the BLR technique was more effective in increasing hamstring muscle flexibility compared to the TSLR technique. Furthermore, Bhosle and Rizvi investigated the treatment of sewing machine operators with hamstring tightness and low back pain, finding that both Mulligan BLR and TSLR techniques were effective in increasing hamstring flexibility and reducing low back pain-related disability, with no significant superiority of one technique over the other.

A review of the current literature reveals conflicting results regarding the efficacy of these techniques on hamstring flexibility. Furthermore, no study to date has compared these two techniques in terms of spatiotemporal gait parameters and pelvic oscillations. Therefore, the purpose of this study is to compare the effects of Mulligan TSLR and BLR techniques on hamstring flexibility, spatiotemporal gait parameters, and pelvic oscillations in individuals with hamstring tightness.

Type d'étude

Interventionnel

Inscription (Réel)

34

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 35 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Individuals between the ages of 18 and 35
  • Individuals who bilateral hamstring shortness

Exclusion Criteria:

  • A passive knee extension angle of 20° or less
  • A history of lower extremity pain or injury within the last 6 months
  • Previous lower extremity surgery
  • Neurological, rheumatological, or systemic diseases
  • Poor cooperation for activities
  • Regular participation in sports.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Seul

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Mulligan Bent Leg Raise (BLR) Technique

17 individuals in this group, after evaluations, mobilization with movement technique applied by clinians and after that same evaluations will be applied.

The participant's flexed knee was supported on the therapist's shoulder. Following a resisted leg push and relaxation, the therapist passively moved the knee toward the ipsilateral shoulder to the maximum pain-free range. If pain occurred, the leg was shifted medially or laterally to find a pain-free pathway.

Expérimental: Mulligan Traction Straight Leg Raise (TSLR) Technique

17 individuals in this group, after evaluations, mobilization with movement technique applied by clinians and after that same evaluations will be applied.

In a supine position with the knee extended and hip neutral, maximum longitudinal traction was applied to the lower extremity. The limb was passively raised (SLR) until the onset of discomfort and immediately returned to the resting position. If pain was indicated, the movement direction was modified by adding abduction and/or rotation to ensure a pain-free pathway.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Passive knee extension test
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

the participant was supine with the tested hip flexed to 90° and the femur stabilized. The contralateral leg remained flat on the table. A goniometer was placed with its axis on the lateral femoral epicondyle, the stationary arm aligned with the greater trochanter, and the moving arm with the lateral malleolus. The knee was passively extended until a stretch was felt or hip flexion was compromised, marking the test endpoint.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Cadence (step / min) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

"Cadence" (steps/min) is the number of steps in a minute. Cadence during gait was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Speed (m / s) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later

Speed (m/s) parameters is average walking speed. Speed during gait was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later
Gait cycle duration (s) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later

Gait cycle duration (s) parameter is average value of the time interval between two consecutive heel strikes of the same foot. Gait cycle duration were assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later
Stride length (m) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

Stride length (m) is the average value of distances between each initial contact and the next one of the same side. Stride length during gait was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Stance phase (% cycle) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

Stance phase (% cycle) is the average value of the duration of the right and left foot support phase as percentage of the gait cycle. Stance phase during gait was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Swing phase (% cycle) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

Swing phase (% cycle) is average value of the duration of the right and left swing phase as percentage of the gait cycle. Swing phase during gait was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Pelvic tilt range (degrees) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

The angles average value described by the pelvis in the 3 main body planes (sagittal, frontal and transversal), are represented in three graphs: The sagittal plane component describes the pelvic tilt. Pelvic tilt range during gait were assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Pelvic obliquity range (degrees) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

The angles average value described by the pelvis in the 3 main body planes (sagittal, frontal and transversal), are represented in three graphs: the frontal plane component describes the pelvic obliquity. Pelvic obliquity range during gait analysis was assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.
Pelvic rotation range (degrees) during gait
Délai: Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

The angles average value described by the pelvis in the 3 main body planes (sagittal, frontal and transversal), are represented in three graphs: the transversal plane component describes the pelvic rotation. Pelvic rotation range during gait were assessed using a BTS G-Walk accelerometer secured at the L4-L5 level. Participants walked at a normal pace along a 10-meter marked track and returned. Data were transmitted via Bluetooth to G-Studio software for analysis.

Measurements were taken at three time points: before the intervention, immediately following the intervention, and 24 hours later.

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

20 juin 2025

Achèvement primaire (Réel)

1 septembre 2025

Achèvement de l'étude (Réel)

10 janvier 2026

Dates d'inscription aux études

Première soumission

14 septembre 2026

Première soumission répondant aux critères de contrôle qualité

25 septembre 2026

Première publication (Réel)

29 septembre 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

29 septembre 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

25 septembre 2026

Dernière vérification

1 septembre 2026

Plus d'information

Termes liés à cette étude

Termes MeSH pertinents supplémentaires

Autres numéros d'identification d'étude

  • 2025 - 977

Plan pour les données individuelles des participants (IPD)

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NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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