Effects of Bin Therapy on Finger Gnosia And Fine Motor Skill

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-05-14

Study Completion Date

2024-08-20

Brief Summary

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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

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Detailed Description

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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

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Down Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

it will be randomized control trial in which non probability convenient sampling will be used. Two groups of age 6-12 will be formed in which participants will be randomly divided. Group A will receive conventional physical therapy exercise program including core strengthening, balance and coordination exercise, fine motor activities and group b will receive BIN therapy and finger gnosia

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

participants will get separate treatment protocols and possible efforts will be put to mask the the both group about treatment

Study Groups

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conventional physical therapy

Control Group

Group Type EXPERIMENTAL

conventional therapy

Intervention Type OTHER

schedule conventional therapy with 20-50 minutes of each session with each set comprises of 10-12 repetitions of each exercise

bin therapy and finger gnosia

Experimental Group

Group Type EXPERIMENTAL

Bin therapy and finger gnosia

Intervention Type OTHER

Schedule 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

Interventions

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Bin therapy and finger gnosia

Schedule 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

Intervention Type OTHER

conventional therapy

schedule conventional therapy with 20-50 minutes of each session with each set comprises of 10-12 repetitions of each exercise

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age range between 5-13 years
* Children with Down syndrome who are able to follow simple instructions.
* Medically stable participants can participate in therapeutic procedures.
* Participants and their families should be able to attend Bin Therapy weekly.

Exclusion Criteria

* Any other medical conditions or cognitive impairments that could affect their participation in the study.
* History of seizures.
* History of heart problems

Minimum Eligible Age

5 Years

Maximum Eligible Age

13 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No