Biofeedback Training's Impact on Cognitive and Motor Skills in Kids With Intellectual Disabilities

Effect of Biofeedback Training on Cognitive and Motor Functions in Children With Intellectual Disabilities

The expected outcome of the study is to confirm or reject the hypothesis that traditional rehabilitation in combined with biofeedback training produces better results in improving motor and cognitive functions, relative to conventional rehabilitation.

In addition, the result of the study will be a protocol for dealing with school-aged children school-age children with impaired motor functions associated with impaired cognitive functions.

The developed material, will be a practical addition to therapeutic programs, Particularly useful in the work of psychological and pedagogical clinics, in offices of rehabilitation and sensory integration offices, or centers implementing early childhood development supporting child development.

Study Overview

• Status: Recruiting
• Conditions: Intellectual Disability, Mild
• Intervention / Treatment: Other: Biofeedback method; Other: Conventional therapy program

Detailed Description

In accordance with the study design, children with intellectual disabilities who will participate in a 3-week rehabilitation program will be eligible for the study.

The research will be a single-center study. The research will be conducted at the St. Hedwig the Queen Regional Hospital No. 2, Lwowska 60, 35-301 Rzeszów - Department of Child Neurology and Pediatrics.

Number of subjects included in the study: The planned group size is 60 people (30 people - study group, 30 people - control group). The given population was calculated on the basis of the sampling calculator " PLUS module " Statistica 13.3 software, taking into account the following parameters: fraction size, confidence level, maximum error.

For the study of the effect of biofeedback training on cognitive and motor function in children with intellectual disabilities, there is no need to recruit healthy participants to the control group.

Prior to the actual study, a pilot study will be conducted on a smaller group of test subjects. After taking into account the eligibility criteria, the subjects will be assigned, on the basis of random selection random assignment, to two groups: the study group - implementing the conventional therapy program supplemented additionally with visual and auditory biofeedback training on a dynamic balance platform, the control - implementing only the conventional therapy program.

Respondents from both groups will participate in a 3-week therapy program, under the same conditions using the same measuring instruments. All participants will be informed about the purpose and conduct of the study and, after consenting to the study, will be qualified for the study proper. The participation of the child called "Minor" in this study depends solely on the parent or legal guardian's expression of consent by signing the Informed Consent Form after reading the information presented information about the study being conducted.

The examination will be performed twice, the initial one before the start of therapy, and the control one after the 3-week rehabilitation program has been completed. The following tools will be used to evaluate the effects of rehabilitation: AMTI dynamography platform, Romberg Test, Up and Go Test - assessment of static and dynanmic balance, ZEBRIS computer system - assessment of posture, HEG Biofeedback (hemoencephalography) - assessment of concentration and attention, AVLT (AuditoryVerbal Lerning Test), Bourdon-Wiersma Test - assessment of cognitive functions, Southern California Sensory Integration Test - assessment of sensory function, Box and Block Test, dynamometer - assessment of hand function, Eurofit Special Test - assessment of physical fitness, PedsQLTM Pediatric Quality of Life Questionnaire - assessment of quality of life, Barthel Scale - assessment of functional ability.

The examination time for one participant will be 1.5 hours. A period of 12 months is planned for recruitment and examination of participants.

The planned study does not involve any risks and possible health hazards for the participants examination. The conducted examination will be completely painless and non-invasive with dignity and principles of intimacy for each patient. The examination will be conducted using measuring devices certified and approved for use within the framework of scientific research in the field of rehabilitation.

The expected outcome of the study is to confirm or reject the hypothesis that traditional rehabilitation combined with biofeedback training produces better results in improving motor and cognitive functions, compared to conventional rehabilitation.

Description of benefits to study participants:

Improved motor and cognitive functions of children with intellectual disabilities, protocol rehabilitation management for children with intellectual disabilities.

• Study Type: Interventional
• Enrollment (Estimated): 60
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Aleksandra Ewa Kiper, MSc; Phone Number: +48607974712; Email: akiper94@gmail.com

Study Locations

• Poland
  • Rzeszów, Poland, 35-959
    • Recruiting
    • University of Rzeszów
    • Contact: Aleksandra Ewa Kiper, MSc; Phone Number: +48607974712; Email: akiper94@gmail.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• diagnosed mild intellectual disability,
• age 7-12 years,
• current health status allowing the child to participate in the study and participate in the rehabilitation program,
• informed voluntary consent of parents and/or legal guardians to participate in the study.

Exclusion Criteria:

• diagnosed intellectual disability of severe and profound degree,
• cognitive deficits impairing the ability to understand and follow instructions,
• age below 7 or above 12 years,
• coexistence of autism, Down syndrome, cerebral palsy, muscular dystrophy and neurological disorders, such as epilepsy or brain damage,
• the presence of comorbidities such as rheumatic, orthopedic, oncological or cardiac diseases that may affect the subject's motor impairment.
• the lack of informed voluntary consent from parents and/or legal guardians to participate in the study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: biofeedback-based therapy (BBT); study group - implementing the conventional therapy program supplemented additionally by training with visual and auditory biofeedback on a dynamic balance platform	Other: Biofeedback method; Study group - implementing a conventional therapy program supplemented additionally with visual and auditory biofeedback training on a dynamic balance platform; Other Names: Conventional therapy program; Other: Conventional therapy program; Control group - rehabilitation management aimed at improving cognitive and motor functions in children with mild intellectual disabilities.
Other: conventional therapy program (CT); control group - implementing only the conventional therapy program	Other: Conventional therapy program; Control group - rehabilitation management aimed at improving cognitive and motor functions in children with mild intellectual disabilities.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessment of static and dynamic balance using the AMTI platform	AMTI platform use is to assess balance ability.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program.
Posture assessment using the computer-based ZEBRIS system	Zebris device allows non-invasive assessment of the shape of the curvature of the spine and parameters that determine postural disorders. The ZEBRIS system consists of a measuring unit, a system of micro-sensors and an ultrasonic pointer, with which topographic points are scanned from the skeleton and then processed in a computer program in the form of a report containing numerical data specifying lengths, angles and degrees for each parameter, as well as graphs and figures of the spinal line.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program.
Assessment of concentration and attention with HEG Biofeedback (hemoencephalography)	Hemoencephalography (HEG) is a method of monitoring changes in frontal cerebral blood circulation and oxygenation. HEG biofeedback is a method based on the use of near-infrared technology to measure cerebral hemodynamics. A sensor armband is placed on the head in the area where reduced blood oxygenation is noted, and then emits into the brain, two beams of light at different frequencies. This allows us to check the oxygen saturation in a particular area of the brain in real time. The signal is returned to the computer screen, and the trainer tries to increase it. HEG biofeedback training involves stimulating neurons in the frontal lobes of the brain.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Assessment of functional by Barthel Scale	Based on the scores assigned the patient's condition is described in the following way: I. 86-100 points - "slight" dependency; II. 21- 85 points - "moderately severe" dependency; III. 0 - 20 points - "severe" dependency. ability	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program.
Quality of life assessment using the PedsQLTM Pediatric Quality of Life Questionnaire	The PedsQL is based on a modular approach to measuring health-related quality of life and consists of a 15-item core measure of global health-related quality of life .	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Assessment of cognitive function using the AVLT test	Involves five sequential presentations of a 15-word list.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Assessment of cognitive function using the Bourdon-Wiersma test	The Bourdon test is an approach to measuring focus and attention that requires the test taker to detect and cross out specific characters in a set of letters.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Manual skills, assessed with Box and Blocks test	The test uses a wooden box, divided into two equal parts by a partition, as well as 150 blocks. The subject moves as many blocks as possible from one part of the box to the other during 60 seconds.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Romberg test	The Romberg test is used to assess static balance. The test involves standing with your feet together and your arms at your side or crossed in front of you. Part of the test is with your eyes open, and the second part is with your eyes closed.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
TUG test	In the TUG test subjects are asked to rise from a standard armchair, walk to a marker 3 m away, turn, walk back, and sit down again.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Southern California Sensory Integration Test - Bilateral Motor Coordination	This test gives information about the motor activity of both sides of the body, sense of rhythm and sequence.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Southern California Sensory Integration Test - Crossing the Body's Midline	This test gives information about the rate and quality of cooperation between the brain hemispheres.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Southern California Sensory Integration Test - Graphesthesia	This test gives information about the ability to visualize tactile stimuli from the top of the hand area and visuomotor coordination.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program
Southern California Sensory Integration Test - Differentiating Right from Left	This test gives information about distinguishing the sides of the body.	First examination - before the start of the rehabilitation program; second examination - at the end of the three-week program

Collaborators and Investigators

• Sponsor: Aleksandra Kiper

Study record dates

Study Major Dates

• Study Start (Estimated): November 1, 2023
• Primary Completion (Estimated): June 1, 2024
• Study Completion (Estimated): January 1, 2025

Study Registration Dates

• First Submitted: October 14, 2023
• First Submitted That Met QC Criteria: November 1, 2023
• First Posted (Actual): November 7, 2023

Study Record Updates

• Last Update Posted (Actual): November 7, 2023
• Last Update Submitted That Met QC Criteria: November 1, 2023
• Last Verified: November 1, 2023

More Information

Terms related to this study

• Keywords: biofeedback; rehabilitation; cognitive function; training; motor function; intellectual disability
• Additional Relevant MeSH Terms: Mental Disorders; Nervous System Diseases; Neurologic Manifestations; Neurobehavioral Manifestations; Neurodevelopmental Disorders; Intellectual Disability
• Other Study ID Numbers: 2023/07/48

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No