Benefits of a Belly Dance Psychomotor Intervention

May 30, 2024 updated by: Simone Leara Barroso Pereira, University of Évora

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.

Study Overview

Status

Active, not recruiting

Conditions

Intervention / Treatment

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.

Study Type

Interventional

Enrollment (Actual)

21

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Évora, Portugal
        • Simone Leara Barroso Pereira

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • 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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Control and Experimental Group
The 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.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
Balance and Postural Control outcome measure assessed by Modified Star Excursion Balance Test (MSEBT); stand stork test and standing stork test (blind).
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
Agility outcome measure assessed by Hexagonal Obstacle Test.
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
Rhythm perception and reproduction assessed by Go No Go Test
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
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).
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
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).
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
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".
[ 0, 6 weeks] vs. [0,12 weeks]
Change from Baseline to post control and to post intervention
Time Frame: [ 0, 6 weeks] vs. [0,12 weeks]
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".
[ 0, 6 weeks] vs. [0,12 weeks]

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 1, 2024

Primary Completion (Estimated)

September 30, 2024

Study Completion (Estimated)

October 30, 2024

Study Registration Dates

First Submitted

May 30, 2024

First Submitted That Met QC Criteria

May 30, 2024

First Posted (Estimated)

June 4, 2024

Study Record Updates

Last Update Posted (Estimated)

June 4, 2024

Last Update Submitted That Met QC Criteria

May 30, 2024

Last Verified

May 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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