Effects of Jive Dance Training on Lower Limb Muscle Strength (NCT07641465) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Effects of Jive Dance Training on Lower Limb Muscle Strength
Taiwan20 participantsStarted 2025-10-21
Plain-language summary
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.
Who can participate
Age range
18 Years – 65 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Change in Bilateral Lower Limb Plantar Flexion Muscle Strength
Timeframe: Baseline (T0), Week 4 (T4), and Week 8 (T8)