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Effects of Adding End-Range Isometric Holds to Isotonic Knee Extensor Training on Isokinetic Performance in Sedentary Adults

25 juin 2026 mis à jour par: Feyza Sule BADILLI HANTAL, Yeditepe University

Effects of Adding End-Range Isometric Holds to Isotonic Knee Extensor Training on Isokinetic Performance in Sedentary Adults: A Randomized Controlled Trial

The goal of this clinical trial is to learn if adding a short muscle hold (isometric contraction) to a standard leg-strengthening exercise improves knee muscle strength more than the standard exercise alone, in healthy adults who do not exercise regularly. The main question it aims to answer is:

Does adding a 5-second hold at the end of each leg-extension exercise lead to greater gains in front-thigh muscle (quadriceps) strength than leg-extension exercise alone?

Researchers will compare two exercise groups to see if the added muscle hold makes a difference:

Group 1 will do leg-extension exercises with a 5-second hold added at the end of each repetition.

Group 2 will do the same leg-extension exercises without the added hold.

Participants will:

Do leg-extension exercises 3 days a week for 8 weeks Have their thigh muscle strength tested before and after the program using a special exercise machine Have their thigh size measured before and after the program

Aperçu de l'étude

Description détaillée

Quadriceps femoris weakness is associated with several musculoskeletal conditions, including knee osteoarthritis, and is a common target of physiotherapy strengthening protocols. While isotonic and isokinetic strengthening methods have each been studied separately, it remains unclear whether adding an isometric hold to isotonic exercise provides additional benefit in isokinetic strength outcomes. This study addressed that question.

This was a randomized, two-arm study conducted at the Sportomed Sports Health and Orthopedic Rehabilitation Clinic (December 2014-May 2015). Forty-six sedentary, healthy adults aged 18-40 years were enrolled, with 43 completing the 8-week protocol. Exclusion criteria included lower-extremity musculoskeletal problems, prior lower-extremity surgery or significant trauma, low back pain, cardiac or neurological conditions, and chronic systemic disease. The study was approved by the Istanbul Medipol University Non-Interventional Clinical Research Ethics Committee (decision no. 257, 07.11.2014), and written informed consent was obtained from all participants.

Participants were randomized to two groups. Both performed isotonic knee-extension exercise (2 sets × 10 repetitions, 60% of 1RM) 3 days/week for 8 weeks, with weekly load progression (~5%) and 60 seconds rest between sets. Group 1 (n=21) added a 5-second isometric hold at 0° knee extension at the end of each repetition; Group 2 (n=22) performed the isotonic protocol without this addition.

Outcomes were assessed at baseline and after 8 weeks: thigh circumference, 1RM isotonic quadriceps strength, and isokinetic peak torque (PT, Nm) at 60°/second and 180°/second using a CSMI Humac Norm 2004 dynamometer. Baseline assessments also included range of motion, manual muscle testing, and physical activity level (IPAQ Short Form).

Statistical analysis was performed using NCSS 2007. Normality was assessed with Shapiro-Wilk testing. Between-group comparisons used independent t-tests or Mann-Whitney U tests as appropriate; within-group pre-post comparisons used paired t-tests. Categorical variables were compared using chi-square testing, and correlations using Pearson testing. Significance was set at p<0.05.

Type d'étude

Interventionnel

Inscription (Réel)

43

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

    • Bostancı/Kadıköy
      • Istanbul, Bostancı/Kadıköy, Turquie (Türkiye), 34744
        • Sportomed | Physical Therapy and Rehabilitation Center

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

  • Adulte

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Age 18-40 years
  • Sedentary lifestyle (low physical activity level)
  • Healthy individuals with no known knee-related disability

Exclusion Criteria:

  • Musculoskeletal problems of the lower extremity
  • History of lower extremity surgery or significant trauma
  • Low back pain and/or lumbar region problems
  • Cardiac complaints
  • Neurological complaints
  • Chronic systemic disease (e.g., diabetes mellitus, rheumatologic conditions)

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: Isotonic + Isometric Hold Group
Participants performed isotonic knee-extension exercise (2 sets of 10 repetitions at 60% of 1-repetition maximum) using a leg-extension machine, 3 days per week for 8 weeks, with weekly load progression (~5%) and 60 seconds of rest between sets. At the end of each repetition, participants held the lifted weight for 5 seconds at 0° knee extension (isometric contraction) before returning to the starting position.
Isotonic knee-extension exercise (2 sets of 10 repetitions at 60% of 1-repetition maximum) performed 3 days per week for 8 weeks, with weekly load progression (~5%) and 60 seconds of rest between sets. Each repetition concluded with a 5-second isometric hold of the lifted weight at 0° knee extension.
Comparateur actif: Isotonic Only Group
Participants performed the same isotonic knee-extension exercise protocol (2 sets of 10 repetitions at 60% of 1-repetition maximum) using a leg-extension machine, 3 days per week for 8 weeks, with weekly load progression (~5%) and 60 seconds of rest between sets, without the addition of an isometric hold at the end of each repetition.
Isotonic knee-extension exercise (2 sets of 10 repetitions at 60% of 1-repetition maximum) performed 3 days per week for 8 weeks, with weekly load progression (~5%) and 60 seconds of rest between sets, without an added isometric hold.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in Quadriceps Femoris Isokinetic Peak Torque
Délai: Baseline and 8 weeks
Quadriceps femoris isokinetic peak torque (PT, Nm) was measured bilaterally using a CSMI Humac Norm 2004 isokinetic dynamometer at angular velocities of 60°/second (5 maximal repetitions) and 180°/second (15 maximal repetitions).
Baseline and 8 weeks

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in Quadriceps Femoris 1-Repetition Maximum (1RM) Isotonic Strength
Délai: Baseline and 8 weeks
Quadriceps femoris 1-repetition maximum isotonic strength was measured bilaterally using a leg-extension apparatus, with each disk increment corresponding to 10 lbs (4.54 kg).
Baseline and 8 weeks
Change in Thigh Circumference
Délai: Baseline and 8 weeks
Thigh circumference was measured bilaterally, 15 cm proximal to the superior border of the patella, using a measuring tape, in the supine position.
Baseline and 8 weeks

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Directeur d'études: Feyza Şule Hantal, PhD, Yeditepe University

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)

12 décembre 2014

Achèvement primaire (Réel)

26 mai 2015

Achèvement de l'étude (Réel)

6 juillet 2015

Dates d'inscription aux études

Première soumission

19 juin 2026

Première soumission répondant aux critères de contrôle qualité

24 juin 2026

Première publication (Réel)

25 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

25 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

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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