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EFFECTS OF DEEP WATER CORE EXERCİSES ON BALANCE AND MUSCLE STRENGTH İN SEDENTARY WOMEN (DWCE)

20 mai 2026 mis à jour par: Ibrahim CAN, Igdir University

INVESTİGATİON OF THE EFFECTS OF DEEP WATER CORE STRENGTHENİNG EXERCİSES ON BALANCE AND MUSCLE STRENGTH İN SEDENTARY INDİVİDUALS

The aim of these clinical trials is to investigate the current effects of a 12-week deep-sea exercise program on sedentary, balance, and muscle strength. The key questions the study aimed to answer were:

  • Does deep-sea exercise improve the development of sedentary dynamic and static balance?
  • Does deep-sea exercise increase upper and lower extremity muscle strength?

Researchers compared an exercise group to a control group to assess exercise performance.

The experimental groups performed deep-sea exercises three times a week for 12 weeks. Dynamic balance, static balance, and muscle strength measurements were assessed at baseline, week 4, week 8, and week 12.

Aperçu de l'étude

Description détaillée

Background: Aquatic physical exercise is becoming increasingly important in preventing loss of strength and balance caused by sedentary lifestyles, a critical public health issue. Therefore, the effects of deep-water abdominal strengthening exercises on balance and muscle strength in sedentary women were investigated.

Methods: A total of 16 sedentary women volunteered to participate in the study. Participants were randomly assigned to experimental and control groups, with an equal number of participants in each group. The experimental group participated in a deep-water abdominal strengthening exercise program three days a week for 12 weeks, while the control group did not participate in any exercise intervention. Participants underwent static and dynamic balance tests at four time points (baseline, weeks 4, 8, and 12), as well as one-repetition maximum (1RM) strength tests for the shoulder, chest, and leg regions.

Type d'étude

Interventionnel

Inscription (Réel)

16

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

    • Batman
      • Batman, Batman, Turquie (Türkiye), 72000
        • Semi-Olympic Indoor Swimming Pool, Batman Municipality

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

Non

La description

Inclusion Criteria:Participant inclusion criteria were: (i) not having suffered any orthopedic injury (fracture, dislocation, serious musculoskeletal injury, etc.) in the past six months, (ii) being able to easily perform the exercises in the pool, (iii) having basic swimming skills to ensure their safety, and (v) committing to fully participating in 12 weeks of exercise programs and measurements.

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Exclusion Criteria:Exclusion criteria are (i) taking any medication that could negatively affect study results and (ii) having a health condition that would prevent them from entering the water (infection, aquaphobia, or skin diseases, etc.). To maintain the study's achievements, participants who missed more than 20% (i.e., 8 or more) of the total exercise sessions during the 12-week intervention period were excluded from the study.

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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: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Experimental Group
The experimental group is undergoing a deep-sea strengthening exercise program three days a week for 12 weeks. The exercise program included water-based core stabilization and strengthening exercises performed in deep water conditions.
Participants underwent a deep-water core strengthening exercise program in a semi-Olympic indoor swimming pool three days a week for 12 weeks under the supervision of researchers. Each exercise session lasted approximately 45 minutes and consisted of warm-up, core strengthening, and cool-down sections. The exercise program was planned according to the principle of progressive loading, and the number of sets and repetitions was gradually increased throughout the process. During the exercise sessions, one instructor actively guided the participants in the pool while another instructor observed and monitored from outside the pool. Adaptation sessions were conducted before the study to ensure the participants adapted to the water. Muscle strength and balance measurements were evaluated at baseline and at weeks 4, 8, and 12. No exercise-related injuries or adverse events were observed during the study.
Autres noms:
  • Aquatic Core Exercise
Aucune intervention: Control Group
Participants in the control group did not participate in any structured exercise intervention during the study period.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Assessment of physical activity level (IPAQ)
Délai: Baseline
To assess the physical activity levels of the participants, the International Economic Activity Questionnaire (IPAQ) consisting of document and 7 questions was used by Craig et al. The survey includes questions aimed at collecting information about the frequency and duration of low, moderate, and high-intensity physical activity lasting at least 10 minutes over the past 7 days.The amount of energy required for activities is calculated using metabolic equivalents (MET). To evaluate the scale, the MET value of each item is multiplied by the duration and day score to obtain the total physical activity score (METmin/week). A score below 600 indicates low-intensity physical activity, a score between 600 and 3000 indicates moderate-intensity, and a score above 3000 indicates vigorous physical activity
Baseline
Dynamic Balance Performance
Délai: Baseline, week 4, week 8, and week 12
Dynamic balance performance was assessed using the Y Balance Test. Participants performed single-leg reach movements on a stable surface in the front, back inward, and back outward directions. During the test, individuals were instructed to hold their hands at hip level and place their heels on the ground. They were also instructed to lightly touch the furthest point of the outstretched leg with their toes. It was stated that the test would be repeated in case of any deviations from the protocol, such as falling, full landing, or the other foot touching the ground. Three trials were performed in each direction, and the average was recorded in centimeters. After recording the measurement data, the percentage maximum reach distance (%MaxD) was normalized according to limb length using the formula: (reach distance/limb length) × 100 = %MAXD. This normalization allows for consistent comparisons, both between right and left limbs and among participants, taking into account variations in li
Baseline, week 4, week 8, and week 12
Static Balance
Délai: Baseline, week 4, week 8, and week 12
Participants' static balance was determined using the Flamingo balance test. A board measuring 50 cm long, 4 cm high, and 3 cm wide was used to administer the Flamingo balance test. Individuals were instructed to place their preferred foot in the center of the balance platform, keep their knee at maximum flexion with their hand on the same side, and focus on a fixed point at eye level. The test lasted 1 minute (60 seconds), and the duration was monitored with a stopwatch. The stopwatch was started when the individual was ready to maintain balance, and each instance of the individual losing balance and placing their other foot on the ground was recorded as a loss of balance within 60 seconds. During this time, the timer was stopped at each loss of balance, and the individual was allowed to reposition themselves. If the individual experienced more than 15 losses of balance within 30 seconds, the test was terminated early. The balance test was administered to participants three times, an
Baseline, week 4, week 8, and week 12
One Repetition Maximum (1RM) Strength
Délai: Baseline, week 4, week 8, and week 12
Participants' maximum strength values in the shoulder, chest, and leg regions were obtained using a one-repetition maximum (1RM) test procedure in 3 different exercises (shoulder press, bench press, and leg press). To determine 1RM, participants performed 5 repetitions using an estimated weight. Then, the load was decreased or increased by 3.5-10 kg in each phase until the correct 1RM value was found using the correct technique, and the test continued. The test was terminated when the individual could not complete 5 repetitions, and a 3-5 minute rest period was given between all trials requiring maximum effort to reach 1RM with the final weight between 3 and 5 repetitions. The maximum strength values of the individuals were determined using the following formula: 1RM Formula: 100 x load (kg) / (102.78 - 2.78 x number of repetitions). The weight successfully lifted was recorded as the maximum strength value.
Baseline, week 4, week 8, and week 12

Collaborateurs et enquêteurs

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

Parrainer

Les enquêteurs

  • Chercheur principal: İbrahim CAN, Professor, Faculty of Sports Sciences, Iğdır University
  • Directeur d'études: Merve C KARTAL, PhD in Sports Sciences, Batman Municipality Sports Affairs Directorate

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)

8 décembre 2024

Achèvement primaire (Réel)

3 mars 2025

Achèvement de l'étude (Réel)

3 mars 2025

Dates d'inscription aux études

Première soumission

20 mai 2026

Première soumission répondant aux critères de contrôle qualité

20 mai 2026

Première publication (Réel)

27 mai 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

27 mai 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

20 mai 2026

Dernière vérification

1 mai 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • DWCE-2024-01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

Individual participant data will not be shared in order to protect participant privacy and confidentiality.

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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