NCT07735468

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for not_applicable hypertension

Timeline
Completed

Started Apr 2026

Shorter than P25 for not_applicable hypertension

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 6, 2026

Completed
4 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 10, 2026

Completed
14 days until next milestone

First Submitted

Initial submission to the registry

July 24, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

July 30, 2026

Completed
Last Updated

July 30, 2026

Status Verified

April 1, 2026

Enrollment Period

2 months

First QC Date

July 24, 2026

Last Update Submit

July 24, 2026

Conditions

Keywords

ZumbaHypertensionBlood PressurePhysical ActivityBody CompositionPsychological Outcomes

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

EXPERIMENTAL

Participants 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.

Behavioral: Zumba fitness programme

Group Control

NO INTERVENTION

Participants 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.

Zumba Group

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Conditions

HypertensionMotor Activity

Condition Hierarchy (Ancestors)

Vascular DiseasesCardiovascular DiseasesBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to either a Zumba-based exercise intervention group or a control group maintaining their usual lifestyle, in a parallel design.
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

Locations