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Effects of Task-oriented Training on Visual-motor Integration and Upper Limb Function in Children With Down Syndrome

R

Riphah International University

Status

Not yet enrolling

Conditions

Down Syndrome

Treatments

Other: conventional therapy
Other: task oriented training

Study type

Interventional

Funder types

Other

Identifiers

NCT06943261
REC/RCR/AHS/25/ Sajal Waheed

Details and patient eligibility

About

The condition known as Down Syndrome (DS) is caused by trisomy 21, or the presence of an extra copy of chromosome 21. DS is the most common survivable autosomal aneuploidy and one of the genetically complicated problem compatible with post-term human survival. Based on current birth prevalence, the prevalence of DS is around 25%-40%. It is one of the most prevalent disease. Visual-motor integration difficulties are common in children with DS, which affects their capacity to synchronize hand movements with vision. This may have an impact on ADLS like writing, eating, grooming. Both delays in motor skills and visual processing might cause difficulties in this domain.

This study will be a randomized controlled trial conducted in spectrum clinic. This study will be completed in time duration of 10 months after approval of synopsis. Non-probability convenience sampling technique will be used and 28 participants will be recruited in study after randomization. Informed consent will be taken from gradians then, the subjects will be divided into two groups and the Group A (Experimental group) will receive task-oriented training 3 times a week which focus on exercises that improve UL function and visual motor coordination and Group B (Control group) will receive general physiotherapy plan and game-based interventions. Poor visual motor skills are one of the inclusion criteria, but significant intellectual disability, prior involvement in related interventions, and untreated medical or psychological conditions are among the exclusion criteria. The data will be assessed at the baseline and after 8th week of treatment. After data collection data will be analyzed by using SPSS version 23.

Enrollment

28 estimated patients

Sex

All

Ages

6 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • • Diagnosed down syndrome patient

    • Both male and female
    • Age range 5 to 12
    • Children who has poor VM skills

Exclusion criteria

  • • Sever intellectual disability

    • Previous participation in similar interventions
    • Uncontrolled medical or psychiatric conditions
    • Low communication skills

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

28 participants in 2 patient groups

Experimental group: task oriented training
Experimental group
Description:
experimental group will receive session of 30 to 45 min of 3 times a week for eight weeks
Treatment:
Other: task oriented training
Other: conventional therapy
control group : conventional therapy and game based interventions
Active Comparator group
Description:
control group will receive session of 30 to 45 min of 3 times a week for eight weeks
Treatment:
Other: task oriented training
Other: conventional therapy

Trial contacts and locations

0

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Central trial contact

Muhammad Asif Javed,, MS-PT; imran amjad, PHD

Data sourced from clinicaltrials.gov

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