Effects of Jive Dance Training on Lower Limb Muscle Strength
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.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Effettivo)
Fase
- Non applicabile
Contatti e Sedi
Luoghi di studio
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Taiwan
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Kaohsiung, Taiwan, Taiwan, 824
- E-Da Cancer Hospital
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Adulto
- Adulto più anziano
Accetta volontari sani
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Prevenzione
- Assegnazione: N / A
- Modello interventistico: Assegnazione di gruppo singolo
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Sperimentale: 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.
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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. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Change in Bilateral Lower Limb Plantar Flexion Muscle Strength
Lasso di tempo: Baseline (T0), Week 4 (T4), and Week 8 (T8)
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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.
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Baseline (T0), Week 4 (T4), and Week 8 (T8)
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Collaboratori e investigatori
Sponsor
Investigatori
- Investigatore principale: YU LING HSU, Clinical Dietitian, E-Da Cancer Hospital
Studiare le date dei record
Studia le date principali
Inizio studio (Effettivo)
Completamento primario (Effettivo)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Altri numeri di identificazione dello studio
- EMRP-114-068
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Descrizione del piano IPD
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
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