Effects of a 10-Week Zumba Program in Adults With Hypertension
ZUMBA-BP
Effects of a 10-Week Zumba-Based Exercise Program on Blood Pressure, Medication Control, Body Composition, and Psychological Outcomes in Adults With Hypertension
1 other identifier
interventional
46
1 country
1
Brief Summary
This study aims to evaluate the effects of a 10-week Zumba-based exercise program performed three times per week on blood pressure in adults with hypertension. In addition to the primary outcome of blood pressure, secondary outcomes including medication control, body composition (body weight, body fat percentage, and muscle mass), and psychological outcomes (anxiety, depression, quality of life, emotional well-being, and sleep quality) will be assessed. Participants will be assigned to either an intervention group, performing the Zumba program, or a control group maintaining their usual lifestyle. Measurements will be conducted at baseline and after the intervention period to determine the effectiveness of the program.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable hypertension
Started Apr 2026
Shorter than P25 for not_applicable hypertension
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
April 27, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 6, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
July 10, 2026
CompletedFirst Submitted
Initial submission to the registry
July 24, 2026
CompletedFirst Posted
Study publicly available on registry
July 30, 2026
CompletedJuly 30, 2026
April 1, 2026
2 months
July 24, 2026
July 24, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Systolic and Diastolic Blood Pressure
Blood pressure will be measured at baseline and after the 10-week intervention using a validated sphygmomanometer.
Baseline and 10 weeks
Study Arms (2)
Zumba Group
EXPERIMENTALParticipants in this group will perform a supervised Zumba-based exercise program for 10 weeks, with a frequency of three sessions per week. Each session will consist of moderate-intensity aerobic exercise based on dance movements.
Group Control
NO INTERVENTIONParticipants in this group will maintain their usual lifestyle and will not participate in the structured exercise program during the study period.
Interventions
Aquí tienes la descripción para el campo de intervención en ClinicalTrials.gov: A 10-week supervised Zumba Fitness programme consisting of three 50-minute sessions per week on non-consecutive days. Each session was structured in three phases: a warm-up (7 minutes), a main part (36 minutes) based on choreographed Latin dance rhythms (merengue, salsa, reggaeton, cumbia, bachata, among others) following a wave-like intensity pattern, and a cool-down (7 minutes). Sessions were led by a certified Zumba Instructor Network (ZIN) instructor with more than 10 years of experience. Internal load was self-regulated by participants using the Borg CR-10 scale, targeting moderate-to-hard effort levels (RPE 4-6). The control group maintained their usual sedentary lifestyle without participating in any structured exercise programme during the intervention period.
Eligibility Criteria
You may qualify if:
- Clinical diagnosis of hypertension defined as SBP ≥ 130 mmHg and/or DBP ≥ 80 mmHg
- Sedentary behaviour during the past 12 months (no regular structured physical activity)
- Age 18 years or older
- Medical clearance to participate in supervised physical activity
- Not having regularly practised Zumba or other dance disciplines during the previous 12 months
You may not qualify if:
- resence of orthopaedic, neurological, or cardiovascular conditions contraindicating exercise
- Unstable or uncontrolled hypertension
- Participation in any other structured exercise programme during the intervention period
- Missing more than 10% of the total sessions (more than 3 sessions)
- Presence of any condition that would prevent safe completion of the programme
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University School of Osuna (University of Seville)
Osuna, Sevilla, 41640, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
July 24, 2026
First Posted
July 30, 2026
Study Start
April 27, 2026
Primary Completion
July 6, 2026
Study Completion
July 10, 2026
Last Updated
July 30, 2026
Record last verified: 2026-04