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Adult WomenNCT06442878

Benefits of a Belly Dance Psychomotor Intervention

A study testing Belly Dance Program in people with Adult Women, run by University of Évora at 1 site in Portugal.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The aim of the present study is to analyze the effects of a psychomotor intervention program mediated by belly dance in adult women. This Quasi-experimental study is a controlled trial with one arm. Participants will be allocated to one group which will be i) control and ii) experimental. Read more about this study

Who is it for?
Ages 18 to 59 years, women onlyHealthy volunteers can take part
Conditions the study is for
Adult Women
What is being tested?
Belly Dance Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
21 participants
Where
1 sitePortugal
Study dates
1 Apr 2024to 30 Oct 2024
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 18 to 59 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Woman aged > 17 years and <60 years
  • Availability to participate in the program

Who cannot join

  • Presence of cognitive impairment (Mini-Mental State Examination);
  • Presence of motor impairment, neurological problems or diseases compromising the program participation;
  • Unavailability to participate in the program.

Trial locations and contacts

1 site in 1 country.

Portugal1 site
  • Simone Leara Barroso Pereira

    Evora

Other trials in Portugal

About this study

Official title: Effects of Psychomotor Intervention Program Mediated by Belly Dance in Adults Women.

The aim of the present study is to analyze the effects of a psychomotor intervention program mediated by belly dance in adult women. This Quasi-experimental study is a controlled trial with one arm. Participants will be allocated to one group which will be i) control and ii) experimental. That is at first i) will attend a control period without intervention (6 weeks) and at second ii) will attend an intervention period participating on the intervention program mediated by belly dance (12 weeks). Participants will be accessed at a baseline, at post control and at post intervention.

Read the detailed description

Sedentary lifestyles has been identified as one of the main causes for the development of pathologies as are cardiovascular diseases and of mental health problems such as anxiety and depression. Associated with this, psychomotor factors can also be negatively affected as well as the perception of well-being. Women's daily life associated with tasks accumulation is referred to as a barrier to engaging in physical have progressively made it more difficult for them to perform formal physical activity (Barranco-Ruiz, 2020). Dance can help in this scenario because it is a pleasurable activity that favors social and intrapersonal relationships, working simultaneously on factors such as balance, motor coordination, agility, body awareness, and rhythm, having a positive impact on quality of life and well-being. In this way, dance, through its various components associated with movement, can assume a character of health promotion, also making possible a space of attention for women (Hernandes et al, 2018). Studies have already been carried out focusing on the effects of belly dancing on body image, quality of life and self-esteem in women with cancer, experienced and professional experienced and professional belly dancers/practitioners, elderly women with depression, pregnant women and depression, pregnant women and those with chronic pain (Boing, 2018; Toberna, 2020; Castrillon, 2017). No studies were found that looked at psychomotor factors (balance, agility and body body awareness), or indicators of well-being focused on body image, movement image and and mood states.

The proposed study has a quasi-experimental design with two pre-tests and one post- test, with only one group, the experimental group being its own control. In this way, we will apply Pre-test 1 and after six weeks without intervention, we will apply Pre-test 2 in order to obtain the results referring to the control group. After that, we will start the intervention itself, which will last twelve weeks and will culminate with the Post test 1.

Conditions
Adult Women
Being tested
Belly Dance Program
Keywords
woman, body awareness, dance, balance and well-being.

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Belly Dance ProgramOther

    All Belly Dance sessions comprised 5 phases: 1) opening ritual (5 min), in which participants will be welcomed and perceived how people were feeling. 2) warm-up (15 min), in which thinking and feeling are integrated during the movements, isolating each part of the body according to Laban's body organization. 3) main phase (30 min), will be proposed individual, pair and group activities, in order to achieve the objectives planned. This phase will end with a choreography composition or a challenge; 4) cool-down (5 min) with stretching and physiological parameters normalization; and 5) ending ritual (5 min), in which the participants will be invented to share their sessions' experience.

Study groups in NCT06442878
Study groupRoleWhat they receive
Control and Experimental GroupOtherThe same group, will do the intervention will attend the belly dance program. The control group will maintain the usually daily activities, not attending any exercise program for a month and a half, and than will be a experimental group with 2 sessions / week of 60 minutes on alternated days.
Receives: Other: Belly Dance Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from Baseline to post control and to post intervention

    Balance and Postural Control outcome measure assessed by Modified Star Excursion Balance Test (MSEBT); stand stork test and standing stork test (blind).

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  2. Change from Baseline to post control and to post intervention

    Agility outcome measure assessed by Hexagonal Obstacle Test.

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  3. Change from Baseline to post control and to post intervention

    Rhythm perception and reproduction assessed by Go No Go Test

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  4. Change from Baseline to post control and to post intervention

    Body Awareness outcome measure assessed by the Multidimensional Assessment of Interoceptive Awareness (MAIA), ranging an 8-scale state-trait questionnaire with 32 items and the Awareness-Body-Chart test (ABC).

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  5. Change from Baseline to post control and to post intervention

    Body Image outcome measure will assessed using the Body Investment Scale (BIS), ranging with a Likert-type scale ranging from 1 (strongly disagree) to 5 (strongly agree).

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  6. Change from Baseline to post control and to post intervention

    Image of movement outcome measure will accessed using the miq-3 test, made up of three subscales to assess the kinesthetic and visual modalities; and two Likert-type subscales with 7 levels of response, ranging from "very difficult" to "very easy".

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

  7. Change from Baseline to post control and to post intervention

    Mood States outcome measure will accessed using the Poms Mood Test with a likert scale with a score of 0 "not at all" and 5 "very much".

    Measured: [ 0, 6 weeks] vs. [0,12 weeks]

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Jun 2024
  2. Study start1 Apr 2024
  3. Primary completion30 Sep 2024 (estimated)
  4. Study completion30 Oct 2024 (estimated)

Resources

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
21 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06442878
Sponsor's protocol ID
UÉ
Status last verified
May 2024
First submitted
30 May 2024
Last updated
4 Jun 2024
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Barranco-Ruiz Y, Paz-Viteri S, Villa-Gonzalez E. Dance Fitness Classes Improve the Health-Related Quality of Life in Sedentary Women. Int J Environ Res Public Health. 2020 May 26;17(11):3771. doi: 10.3390/ijerph17113771.

    PubMed 32466496
  • Boing L, Baptista F, Pereira GS, Sperandio FF, Moratelli J, Cardoso AA, Borgatto AF, de Azevedo Guimaraes AC. Benefits of belly dance on quality of life, fatigue, and depressive symptoms in women with breast cancer - A pilot study of a non-randomised clinical trial. J Bodyw Mov Ther. 2018 Apr;22(2):460-466. doi: 10.1016/j.jbmt.2017.10.003. Epub 2017 Oct 12.

    PubMed 29861250
  • Castrillon T, Hanney WJ, Rothschild CE, Kolber MJ, Liu X, Masaracchio M. The effects of a standardized belly dance program on perceived pain, disability, and function in women with chronic low back pain. J Back Musculoskelet Rehabil. 2017;30(3):477-496. doi: 10.3233/BMR-150504.

    PubMed 27858690
  • Hernandes JC, Di Castro VC, Mendonca ME, Porto CC. Quality of life of women who practice dance: a systematic review protocol. Syst Rev. 2018 Jul 10;7(1):92. doi: 10.1186/s13643-018-0750-5.

    PubMed 29991355
  • Toberna CP, Horter D, Heslin K, Forgie MM, Malloy E, Kram JJF. Dancing During Labor: Social Media Trend or Future Practice? J Patient Cent Res Rev. 2020 Apr 27;7(2):213-217. doi: 10.17294/2330-0698.1723. eCollection 2020 Spring.

    PubMed 32377554

Questions about this trial

What is this clinical trial studying?

A study testing Belly Dance Program in people with Adult Women, run by University of Évora at 1 site in Portugal.

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 2 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: status not confirmed, as of the sponsor's last update on 4 Jun 2024. 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 Portugal. 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?

Results are not available in the source record.

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?

Change from Baseline to post control and to post intervention (time frame: [ 0, 6 weeks] vs. [0,12 weeks]). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06442878, which also lists 5 linked publications.

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 4 Jun 2024.

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