Metabolic SyndromeZumBeatNCT02384694
Effects of a Zumba Dance Program for Postmenopausal Women With Metabolic Syndrome
A study testing Zumba dance in people with Metabolic Syndrome, run by University of Basel at 1 site in Switzerland.
Trial summary
The aim of this study is to examine the effects of a 12-week Zumba dance intervention on fitness, anthropometric and psychometric parameters and eating behavior. Read more about this study
- Who is it for?
- Ages 45 to 65 years, women only
- Conditions the study is for
- Metabolic Syndrome
- What is being tested?
- Zumba dance
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 17 participants
- Where
- 1 siteSwitzerland
- Study dates
- May 2014to Oct 2014
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 45 to 65 years
- Women only
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- postmenopausal women (Age 45-65)
- waist of >94 cm or BMI > 30kg/m2
- not physically active >1x/week for 20 minutes
- written consent before the start of the study
Who cannot join
- involvement in other clinical studies
- unable to participate at the dance lessons
- medical contraindications for the intervention or increased risk for exercise participation
Trial locations and contacts
1 site in 1 country.
Switzerland1 site
Department for Sports, Exercise and Health, Sports and Exercise Medicine, University of Basel
Basel, 4052
About this study
Official title: ZumBeat: Effekte Eines Rhythmusorientierten Aeroben Tanz-Bewegungsprogrammes für Postmenopausale Frauen Mit Metabolischem Syndrom
The aim of this study is to examine the effects of a 12-week Zumba dance intervention on fitness, anthropometric and psychometric parameters and eating behavior.
- Conditions
- Metabolic Syndrome
- Being tested
- Zumba dance
- Keywords
- cardiorespiratory fitness, weight, quality of life, depression, menopausal symptoms, exercise barriers, executive functions
- Medical subject headings
- Metabolic Syndrome, Body Weight, Depression
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Zumba danceOther
Twelve weeks, 3 times weekly 1 hour training
| Study group | Role | What they receive |
|---|---|---|
| Intervention | Experimental | Zumba dance intervention Receives: Other: Zumba dance |
What is being measured
The primary outcome is the main question the study is designed to answer.
VO2peak (=peak oxygen consumption)
The VO2peak will be assessed for every participant during a treadmill spirometry at baseline and follow-up using a mask and calibrated gas measuring devices applying a standardized protocol.
Measured: VO2peak will be assessed at T1 and T12 (baseline and after 12 weeks of intervention)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted10 Mar 2015 (estimated)
- Study startMay 2014
- Primary completionOct 2014
- Study completionOct 2014
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Metabolic SyndromeStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 17 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Basel
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Arno Schmidt-Trucksäss, University of Basel
- Investigators
- Arno Schmidt-Trucksäss, Prof. Dr., Principal investigator, Sports and Exercise Medicine, Department of Sports, Exercise and Health, University of Basel
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02384694
- Sponsor's protocol ID
- EKNZ 2014-033
- Acronym
- ZumBeat
- Status last verified
- Mar 2015
- First submitted
- 27 Feb 2015
- Last updated
- 10 Mar 2015
- Results posted
- No
- Data monitoring committee
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 10 Mar 2015. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- ZumBeat: Effekte Eines Rhythmusorientierten Aeroben Tanz-Bewegungsprogrammes für Postmenopausale Frauen Mit Metabolischem Syndrom
- ClinicalTrials.gov ID
- NCT02384694
- Acronym / sponsor ID
- ZumBeat / EKNZ 2014-033
- Conditions
- Metabolic Syndrome
- Keywords
- cardiorespiratory fitness, weight, quality of life, depression, menopausal symptoms, exercise barriers, executive functions
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 17 participants (actual)
- Lead sponsor
- University of BaselUniversity, hospital or other
- Study start
- May 2014
- Primary completion
- Oct 2014 (actual)
- Study completion
- Oct 2014 (actual)
- First posted
- 10 Mar 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The aim of this study is to examine the effects of a 12-week Zumba dance intervention on fitness, anthropometric and psychometric parameters and eating behavior.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Intervention | Experimental | Other: Zumba danceZumba dance intervention |
Who may qualify
- Ages
- 45 to 65 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (4 listed)
- postmenopausal women (Age 45-65)
- waist of >94 cm or BMI > 30kg/m2
- not physically active >1x/week for 20 minutes
- written consent before the start of the study
Key exclusion criteria (3 listed)
- involvement in other clinical studies
- unable to participate at the dance lessons
- medical contraindications for the intervention or increased risk for exercise participation
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Zumba danceTwelve weeks, 3 times weekly 1 hour training | Other | Intervention |
Primary outcome
VO2peak (=peak oxygen consumption)
Time frame: VO2peak will be assessed at T1 and T12 (baseline and after 12 weeks of intervention)
The VO2peak will be assessed for every participant during a treadmill spirometry at baseline and follow-up using a mask and calibrated gas measuring devices applying a standardized protocol.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 10 Mar 2015.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Arno Schmidt-Trucksäss, Prof. Dr. principal investigator
Sports and Exercise Medicine, Department of Sports, Exercise and Health, University of Basel
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Zumba dance in people with Metabolic Syndrome, run by University of Basel at 1 site in Switzerland.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 10 Mar 2015. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
VO2peak (=peak oxygen consumption) (time frame: VO2peak will be assessed at T1 and T12 (baseline and after 12 weeks of intervention)). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 10 Mar 2015.