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Effects of Jive Dance Training on Lower Limb Muscle Strength

6 juni 2026 uppdaterad av: HSU YU LING, E-DA Hospital

The Health-promoting Effects of Ballroom Dancing Courses on Lower Limb Strength, Dynamic Balance, Body Composition, and Working Memory of Hospital Employees

The purpose of this study is to evaluate the effects of a structured, partner-free Jive dance training program on the physical and cognitive health of hospital employees. Healthcare workers often face high-stress environments, irregular shifts, and prolonged physical strain, which can lead to reduced muscle strength, poor body composition, and burnout. This study innovates by designing a solo Jive dance intervention to overcome traditional partnership limitations in workplace wellness programs.

A single-group repeated measures design was used, recruiting 20 hospital employees for an 8-week study. The study was divided into Phase A (4 weeks of self-directed group practice) and Phase B (4 weeks of systematic Jive dance training). Comprehensive assessments were conducted at baseline, week 4, and week 8 to measure body composition, lower limb muscle strength, dynamic balance, working memory, and perceived stress.

Studieöversikt

Status

Aktiv, inte rekryterande

Studietyp

Interventionell

Inskrivning (Faktisk)

20

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

    • Taiwan
      • Kaohsiung, Taiwan, Taiwan, 824
        • E-Da Cancer Hospital

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Ja

Beskrivning

Inclusion Criteria:

  • Currently employed as a full-time or part-time staff member at the hospital.
  • Aged between 18 and 65 years.
  • Voluntarily willing to participate in the 8-week dance program and complete all sequential phases (Phase A and Phase B).
  • Mentally and physically capable of performing moderate-to-high intensity structured exercise (such as solo Jive dancing).
  • Able to understand the study protocols and provide written informed consent.

Exclusion Criteria:

  • Pre-existing severe musculoskeletal injuries, severe joint degeneration, or acute pain that restricts dancing or weight-shifting movements.
  • Uncontrolled cardiovascular diseases (e.g., severe hypertension, arrhythmia, or unstable angina) that render high-intensity aerobic exercise unsafe.
  • Current pregnancy or plans to become pregnant during the 8-week intervention period.
  • Undergoing regular professional or competitive athletic training that could introduce significant confounding effects to the physical outcomes.
  • Any other medical condition, severe cognitive impairment, or physical limitation judged by the investigator to pose a safety risk during exercise or interfere with data collection.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Förebyggande
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Solo Jive Dance Training Group
All participants in this single group will sequentially undergo two distinct phases over an 8-week period. Phase A involves 4 weeks of self-directed group practice, which serves as the comparison stage. This is immediately followed by Phase B, consisting of 4 weeks of a systematic, structured solo Jive dance training program (60 minutes per session) designed to enhance physical and cognitive functions.

This intervention features an innovative, partner-free "Solo Jive" ballroom dance curriculum designed to overcome the barrier of partner limitations in traditional workplace wellness programs. Distinct from general dance activities, this program is structured into two sequential 4-week phases: a self-directed group practice phase followed by a highly systematic, supervised professional training phase.

The core curriculum emphasizes continuous rhythmic tracking, agility, and fast-paced weight-shifting movements characteristic of Jive, focusing heavily on bilateral lower-limb coordination. It is tailored to address healthcare workers' occupational strains, integrating physical neuromuscular training with cognitive-motor engagement (working memory) to provide a dual-benefit intervention for adult workplace populations.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Change in Bilateral Lower Limb Plantar Flexion Muscle Strength
Tidsram: Baseline (T0), Week 4 (T4), and Week 8 (T8)
Lower limb muscle strength (specifically plantar flexion) is measured to evaluate the neuromuscular effects of the systematic Jive dance training. Measurements are taken using a digital handheld dynamometer. The recorded values are expressed in pounds (lbs) to capture quantitative changes. An increase in the measured force values from baseline indicates an improvement in lower limb muscle strength.
Baseline (T0), Week 4 (T4), and Week 8 (T8)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Sponsor

Utredare

  • Huvudutredare: YU LING HSU, Clinical Dietitian, E-Da Cancer Hospital

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

21 oktober 2025

Primärt slutförande (Faktisk)

12 december 2025

Avslutad studie (Beräknad)

31 juli 2026

Studieregistreringsdatum

Först inskickad

1 juni 2026

Först inskickad som uppfyllde QC-kriterierna

6 juni 2026

Första postat (Faktisk)

11 juni 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

11 juni 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

6 juni 2026

Senast verifierad

1 juni 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • EMRP-114-068

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

IPD-planbeskrivning

To protect participant privacy and comply with institutional data protection regulations, individual participant data will not be publicly shared. The findings will be available through aggregated statistical summaries in subsequent research reports.

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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