Effects of a 10-Week Zumba Program on Anxiety and Depression in Adults
ZUMBA-AN-DE
Effects of 10 Weeks of Zumba Training on Anxiety and Depression: A Randomized Controlled Trial
1 other identifier
interventional
40
1 country
1
Brief Summary
This randomized controlled trial aimed to examine the effects of a 10-week Zumba exercise program on anxiety and depression levels in healthy adults. Participants aged 40 to 65 years were randomly assigned to either a Zumba intervention group or a control group that maintained their usual lifestyle. The intervention consisted of three supervised Zumba sessions per week, each lasting approximately 50 minutes. Anxiety and depression were assessed before and after the intervention using the Hospital Anxiety and Depression Scale (HADS). The study sought to determine whether a structured, group-based aerobic exercise program could improve psychological well-being in a non-clinical adult population.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable anxiety
Started Feb 2025
Shorter than P25 for not_applicable anxiety
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
February 3, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 16, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 16, 2025
CompletedFirst Submitted
Initial submission to the registry
December 19, 2025
CompletedFirst Posted
Study publicly available on registry
January 5, 2026
CompletedJanuary 9, 2026
December 1, 2025
2 months
December 19, 2025
January 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Anxiety and Depression
Anxiety and depression were assessed using the Hospital Anxiety and Depression Scale (HADS), a validated self-report questionnaire designed to detect clinically relevant symptoms of anxiety and depression in non-psychiatric populations. The scale consists of 14 items divided into two subscales: anxiety (HADS-A) and depression (HADS-D), each ranging from 0 to 21 points, with higher scores indicating greater symptom severity. Total HADS scores range from 0 to 42. Changes in total and subscale scores were used to evaluate the effects of the intervention on psychological well-being.
Baseline and Week 10 (end of intervention)
Study Arms (2)
Zumba Group
EXPERIMENTALParticipants assigned to the experimental group formed the Zumba intervention group. This group followed a supervised Zumba-based exercise program over a period of 10 weeks. The intervention consisted of structured group sessions performed several times per week and led by a qualified instructor. Sessions were based on choreographed aerobic dance movements performed to music, providing moderate-to-vigorous intensity physical activity aimed at improving cardiovascular fitness and overall physical engagement.
Group Control
NO INTERVENTIONParticipants in the control group did not participate in the exercise intervention and were instructed to maintain their usual lifestyle and physical activity habits throughout the study period.
Interventions
Participants assigned to this intervention received a supervised Zumba-based exercise program lasting 10 consecutive weeks. The intervention consisted of group-based aerobic dance sessions conducted several times per week and led by a qualified instructor. Sessions included choreographed dance movements performed to music, designed to elicit moderate-to-vigorous physical activity and to promote cardiovascular fitness and overall physical engagement. The program followed a standardized structure across sessions and was implemented as the sole intervention during the study period.
Eligibility Criteria
You may qualify if:
- adults aged between 40 and 65 years
- not having regularly practised Zumba or other dance disciplines during the previous 12 months
- medical authorisation or absence of pathologies to participate in supervised physical activity
You may not qualify if:
- presence of orthopaedic, neurological, cardiorespiratory conditions or lack of standing stability that would prevent safe completion of the programme
- participation in any other structured exercise programme during the intervention period
- missing more than 10% of the total sessions (missing more than 2 sessions)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Osuna fitness
Osuna, Sevilla, 41640, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This was an open-label study. Due to the nature of the exercise intervention, neither participants nor investigators were blinded to group allocation.
- Purpose
- PREVENTION
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
December 19, 2025
First Posted
January 5, 2026
Study Start
February 3, 2025
Primary Completion
April 16, 2025
Study Completion
April 16, 2025
Last Updated
January 9, 2026
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared publicly. The dataset contains sensitive health-related information collected in a supervised exercise intervention and was obtained under informed consent that did not include data sharing. Data may be available from the corresponding author upon reasonable request, subject to ethical approval.