- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06444659
Effects of Adaptive Physical Activity on Health-related Fitness of Students With Intellectual Disabilitiesdisability
Effects of Adaptive Physical Activity on Health-related Fitness of Students With Intellectual Disabilities
The object of this study is the theory and practice of adaptive physical activity for people with intellectual disability. It focuses on the concepts, paths, and applications of adaptive physical activities for young people with intellectual disability, and systematically studies and discusses the concepts, paths, and application strategies of adaptive physical activities for young people with intellectual disability, so as to provide solutions and support for the scientific exercise of this special population group. The study will focus on the following four aspects: (1) theoretical research on the interventions of young people with intellectual disability (2) analysis of the sports and health needs of young people with intellectual disability (3) empirical research on adaptive physical activities for young people with intellectual disability (4) exploration of strategies for the use of adaptive physical activities.
Based on theoretical and practical research, to understand the current situation of sports participation and influencing factors of Effects of adaptive physical activity on health-related Fitness and Fundamental Movement Skills in students with intellectual disability , to provide a reliable basis for the formulation of adaptive sports activity programmes suitable for the rehabilitation concepts of the Effects of adaptive physical activity on health-related Fitness and Fundamental Movement Skills in students with intellectual disability; to increase the interest of Effects of adaptive physical activity on health-related Fitness and Fundamental Movement Skills in students with intellectual disability in sports activities, so as to enable them to master the basic sports skills, have the physical abilities required for completing the basic social activities, and be able to participate in sports activities on a regular basis in their future lives; and to promote their physical health and happy lives, with a view to facilitating their integration into regular education and, ultimately, social integration.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Peiying Huang
- Phone Number: 19873081845
- Email: 826901889@qq.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Clinical diagnosis of Intellectual disability
- Agree and promise to participate in the exercise intervention throughout the study programme
- No other physical activity other than participation in school sports
Exclusion Criteria:
- Have other medical conditions that limit physical activity (e.g. asthma, heart disease, etc.)
- Suffers from complex neurological disorders
- unable to play sports due to abnormal physical development
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Adaptive physical activities
|
The intervention group received a 16-week adaptive physical activity intervention; the control group, on the other hand, continued their original regular physical activity programme for the same period of time and maintained their original lifestyle habits.
|
|
No Intervention: Traditional physical education
Continue to carry out the original regular physical education activities during the same period of time, and maintain the original daily habits.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Muscular strength and endurance within Health-Related Physical Fitness are assessed using the handgrip strength test
Time Frame: up to 16 weeks
|
up to 16 weeks
|
|
Body mass index (BMI) was computed based on measurements of weight and height
Time Frame: up to 16 weeks
|
up to 16 weeks
|
|
Body fat percentage
Time Frame: up to 16 weeks
|
up to 16 weeks
|
|
Flexibility was assessed using the Sit-and-Reach test
Time Frame: Pre-intervention, intervention, post-intervention
|
Pre-intervention, intervention, post-intervention
|
|
Cardiopulmonary fitness was assessed via the 20 m PACER run
Time Frame: up to 16 weeks
|
up to 16 weeks
|
|
FMS assessment: The Test of Gross Motor Development-2 (TGMD-2) for assessing participants' FMS development
Time Frame: up to 16 weeks
|
up to 16 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Objective measurement of participants' sleep quality using the Actigraph GT3X+
Time Frame: up to 16 weeks
|
up to 16 weeks
|
|
|
Physical Activity Leves: ActiGraph GT3X+ (ActiGraph LLC, Pensacola, FL) triaxial accelerometers
Time Frame: up to 26 weeks
|
up to 26 weeks
|
|
|
Quality of life : We assessed quality of life (QoL) using the World Health Organization Quality of Life (WHOQOL) scale.
Time Frame: up to 26 weeks
|
Participants responded to 12 items, with each item providing five response options.
The total score ranges from 12 to 60, with higher scores indicating better quality of life.
|
up to 26 weeks
|
|
The Physical Activity Enjoyment Scale (PACES): It is used to assess enjoyment of physical activity.
Time Frame: up to 26 weeks
|
The questionnaire consists of 16 questions rated on a 5-point scale.
The scale consists of 9 positively worded items and 7 negatively worded items.
Scores for the 7 negatively worded items are reverse-coded and then combined with the scores for the positively worded items.
Higher total scores indicate greater levels of enjoyment.
|
up to 26 weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- HunanNU
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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