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Effect of Rhythmic Gymnastics Training in Children With Down Syndrome

Effect of an Adapted Rhythmic Gymnastics Training Program in Children With Down Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06284707
Enrollment
20
Registered
2024-02-29
Start date
2024-03-01
Completion date
2024-05-05
Last updated
2024-05-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical Conditioning, Human

Keywords

rhythmic gymnastics, disability, gymnastics training, down syndrome, child

Brief summary

Some of the clinical characteristics of people with Down syndrome (DS) are orthopedic, cardiovascular, neuromuscular, visual, cognitive and perceptual disorders, which directly affect the quality of their movements. Children with DS often have a sedentary lifestyle or low levels of physical activity which exacerbates problems related to obesity and overall physical health. Therefore, the practice of physical exercise in this type of population is essential to improve their health-related physical fitness. The aim of this study was to analyze the influence of an adapted rhythmic gymnastics training program on body composition, tendon architecture and stiffness, and physical capacity in children with DS.

Detailed description

Children with DS with medium to moderate intellectual disabilities are required to participate. Participants will complete 10 weeks of training, two days per week. They will be divided into two groups: the Control Group will receive two swimming sessions per week and the Experimental Group will receive two swimming sessions plus two rhythmic gymnastics sessions. Before and after the application of the program, the following will be evaluated: body composition by Inbody 720, muscular architecture and elastography by Logiq® S8 ultrasound scanner and tendon stiffness by Myoton® Pro portable myotonometer. The tendons to be studied will be the Achilles tendon and the patellar tendon.

Interventions

OTHERswimming training

2 sessions per week of swimming training

OTHERrhythmic gymnastics training

2 training sessions of rhythmic gymnastics

Sponsors

University of Castilla-La Mancha
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
TRIPLE (Subject, Caregiver, Investigator)

Masking description

The care provider will be responsible for administering the training program. Two different people will develop swimming training and rhythmic gymnastics training. Each participant will be assigned a code. The researcher will process the data with the code of each participant.

Eligibility

Sex/Gender
ALL
Age
6 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* Disabiluty: mild to moderate

Exclusion criteria

* Any contraindication to exercise * Severe or profound intellectual disability * Musculoskeletal disorders that prevented completion of the tests

Design outcomes

Primary

MeasureTime frameDescription
Body compositionbaseline and immediately post interventionBody compisition will be assessed with the Inbody 720 (Bioespace, Seoul, Korea). In this test body mass (BM; kg), muscle mass (MM; kg), fat mass (FM; kg), lean mass (LM; kg), fat-free mass (FF; kg)
Tendon thicknessbaseline and immediately post interventionTendon thickness will be evaluated with the Logiq® S8 ultrasound machine (GE Healthcare, Milwaukee, WI).
Stiffness tendonbaseline and immediately post interventionStiffness tendon will be evaluated with Myoton® Pro hand-held myotonometer (Myoton AS, Tallinn, Estonia). In this test, the mechanical properties of the Achilles tendon will be measured.
Hamstrings flexibilitybaseline and immediately post interventionHamstrings flexibility will be evaluated with Seat and Reach Test (Fabrication Enterprises Inc., USA).
body mass indexbaseline and immediately post interventionBody mass index (BMI; kg/m2) will be calcultated from body mass and height
visceral fat areabaseline and immediately post interventionvisceral fat area (area; cm2) will be assessed with the Inbody 720 (Bioespace, Seoul, Korea).
metabolismbaseline and immediately post interventionmetabolism (MET; kcal) will be assessed with the Inbody 720 (Bioespace, Seoul, Korea).
tendon elastographybaseline and immediately post interventionTendon elastography will be evaluated with the Logiq® S8 ultrasound machine (GE Healthcare, Milwaukee, WI).
balancebaseline and immediately post interventionBalance will be evaluated with the Biodex Balance System stability system (Biodex Medical Systems Inc., USA).
functional capacitybaseline and immediately post interventionFunctional capacity of the lower body wll be evaluated with Sit to Stand Test adapted.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026