Clinical Trials Directory

Trials / Completed

CompletedNCT06576206

Effects of Bin Therapy on Finger Gnosia And Fine Motor Skill

Effects of Bin Therapy on Finger Gnosia and Fine Motor Skills in Children With Down Syndrome

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
30 (actual)
Sponsor
Riphah International University · Academic / Other
Sex
All
Age
5 Years – 13 Years
Healthy volunteers
Not accepted

Summary

Down syndrome is a hereditary disorder resulting from the occurrence of an additional copy of chromosome 21, resulting in discernible variations in cognitive and physical characteristics. Finger gnosis pertains to the capacity to identify and discriminate among individual fingers. Tactile perception and body awareness are both encompassed by this particular component. Finger gnosis encompasses the sensory and cognitive mechanisms that enable an individual to recognize, label, and differentiate between their own fingers and those belonging to others. The therapeutic approach known as BIN Therapy is a non-invasive and pharmacologically unassisted intervention that use electrical stimulation as a means to enhance manual dexterity in individuals afflicted with neurological conditions

Detailed description

It will be a randomized controlled trial. 30 patients fulfilling the inclusion and exclusion criteria will be recruited by non-probability convenience sampling and then randomly divided in two groups using lottery method. Group A will receive will receive conventional physical therapy exercise program including core strengthening, balance and coordination exercise, fine motor skills activities with 2-3 times a week, with 20-50 minutes of each session with each set comprises of 10-12 repetitions of each exercise. And the group B will receive BIN therapy and finger gnosia. Sensory assessment will be assess by Revised Nottingham sensory assessment.

Conditions

Interventions

TypeNameDescription
OTHERBin therapy and finger gnosiaSchedule bin therapy sessions 2-3 times per week at first, increasing the frequency as participants get used to it. Data will be collected twice i.e., at the start of the study and after completion of 6 weeks of treatment by using outcome measure tools
OTHERconventional therapyschedule conventional therapy with 20-50 minutes of each session with each set comprises of 10-12 repetitions of each exercise

Timeline

Start date
2024-05-14
Primary completion
2024-08-17
Completion
2024-08-20
First posted
2024-08-28
Last updated
2024-09-04

Locations

1 site across 1 country: Pakistan

Source: ClinicalTrials.gov record NCT06576206. Inclusion in this directory is not an endorsement.