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Effects of Auditory and Visual Cueing on Sensorimotor Recovery and Gait in Hemiplegia

Primary Purpose

Hemiplegia

Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
Rhtyhmical auditory stimulation and Visual cues (Experimental group)
Rhtyhmical auditory stimulation (Control group)
Sponsored by
Riphah International University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hemiplegia focused on measuring auditory, visual, sensorimotor, hemiplegia, gait

Eligibility Criteria

45 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age range between 45-65 years Both male and female genders Clinically diagnosed of stroke referred by Neuro physician Patients in the chronic stage after 6 months of stroke can walk 10 meters independently. Patients with anterior cerebral artery (ACA) and middle cerebral artery (MCA) involvement with the affected side being the dominant side Those with Brunnstrom's recovery stages 3 and 4 will take part Patients with Mini-Mental State Examination (MMS) score greater than 16. According to Modified Ashworth Scale, patients of grades 1 and 1+ will be included. Muscles that go into the spasticity include hip adductors, knee flexors and ankle plantar flexors Exclusion Criteria: Patients with dementia, depression or productive psychosis will not include. Patients having any visual or auditory impairment will be excluded. Patients with foot drop Recurrent transient ischemic attack (TIA) Patients with recurrent stroke

Sites / Locations

  • Tehreem MukhtarRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Rhtyhmical auditory stimulation and Visual cues (Experimental group)

Rhtyhmical auditory stimulation (control group)

Arm Description

For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. For visual stimulation, white chalk will use to draw visual signals on the ground. For gait recovery, a 10-meter walkway will draw on the floor with parallel lines 2.5cm broad and 90cm long. Interline distance will maintain at 110% of the length of the initial step. Routine rehablitation treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Experimental group will be treated for 45 minutes per session, 3 days per week for 6 weeks.

For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. Routine rehablitation treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Control group will be treated for 45 minutes per session, 3 days per week for 6 weeks.

Outcomes

Primary Outcome Measures

Fugl-Meyer Assessment FMA (LE)
FMA is used to assess sensorimotor function which consists of maximum 28 points for lower extremity and 6 points for speed and coordination. The total summed score of 34 points indicates normal function. Higher the score more is the independence.
Dynamic Gait Index (DGI)
DGI is composed of a total of 8 items. Total score is 24. In total, a score of less than 19/24 is predictive of falls in the elderly. A score of >22 signifies a safe ambulator.
Cadence
Number of steps taken per unit time
Gait velocity/Walking speed
10 min walk test
Stride length
Distance between successive ground contacts of the same foot by using measuring tape.
Step length
Distance between successive ground contact of the opposite foot by using measuring tape.
Step width
Transverse linear distance between two successive feet from the centers of heels by using measuring tape.
Step length symmetry ratio
It will be calculated by dividing step length of paretic limb to non-paretic limb.
Stride length symmetry ratio
It will be calculated by dividing the stride length of paretic limb to non-paretic limb.

Secondary Outcome Measures

Full Information

First Posted
September 22, 2023
Last Updated
September 22, 2023
Sponsor
Riphah International University
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1. Study Identification

Unique Protocol Identification Number
NCT06059781
Brief Title
Effects of Auditory and Visual Cueing on Sensorimotor Recovery and Gait in Hemiplegia
Official Title
Combined Effects of Auditory and Visual Rhythmical Cueing on Lower Limb Sensorimotor Recovery and Gait Parameters in Patients With Hemiplegia
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 1, 2023 (Actual)
Primary Completion Date
December 1, 2023 (Anticipated)
Study Completion Date
December 15, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Riphah International University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Stroke is also known as a brain attack, happens when a blood vessel in the brain breaks or when something stops the flow of blood to a specific area of the brain. Parts of the brain undergo damage or die in either case. Stroke victims may experience permanent brain damage, long-term disability or even death. The main objective of this study is to evaluate the impact of combined auditory and visual rhythmical cueing on lower limb sensorimotor recovery and gait parameters in patients with hemiplegia. It will be a randomized controlled trial. In this study 28 patients will be recruited through non probability convenience sampling technique. The patients fulfilling inclusion and exclusion criteria will be randomly divided into experimental group (n=14) and control group (n=14) by using computer engendered in blocks by using a basic number generator. Distribution will be concealed by the sealed envelope method. Baseline treatment will be given to both groups. Baseline treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Conventional training will be given for 15 minutes, 3 sessions per week for 4 weeks. Experimental group (n=14) will be treated with auditory stimulation and visual cues. All participants will undergo the training for 45 minutes per session, 3 days per week for 4 weeks. The control group (n=14) will be treated with auditory stimulation only. All participants will undergo the training for 45 minutes per session, 3 days per week for 4 weeks. Subjective tool for sensory assessment includes Fugl-Meyer Assessment (FMA) for the lower extremity (LE) tool. For gait, it includes Dynamic Gait Index (DGI) tool. Objective tools will include cadence, gait velocity/walking speed, stride length, step length, step width, stride length symmetry ratio and step length symmetry ratio. Data will be analyzed by using SPSS (Statistical Package for Social Sciences) 23 version.
Detailed Description
A neurological condition known as a stroke is characterized by blood vessel obstruction. Brain clots prevent blood from flowing properly, obstructing arteries and causing blood vessels to burst, which causes bleeding. The abrupt death of brain cells due to a lack of oxygen occurs when the arteries leading to the brain are ruptured during a stroke . Stroke subtypes can be categorized as ischemic or hemorrhagic depending on the etiology. The majority of stroke cases (80-87%) are ischemic strokes, which can be either focal (caused by thrombosis, cardio-embolism, or atherosclerosis and platelets plugging an artery) or global (caused by a complete reduction in blood flow to the brain during a cardiac arrest). Ischemic stroke can also be lethal or not. On the other side, a blood vessel rupture results in hemorrhagic stroke . During a transient ischemic attack (TIA), arterial supply to brain tissue is temporarily cut off, resulting in focal neurologic symptoms such as hemiparesis, but spontaneous flow restoration leads to symptom relief without long-term tissue damage . Gehan M. Ahmed1, Ebtesam M. Fahmy (2023) did an RCT (randomized control trial) study in which they recruited 30 male stroke patients. Group A (control group) was treated with strengthening exercises for weak upper and lower limb, stretching exercises for lower extremity muscles, weight bearing on affected side and treadmill exercises for 6 weeks. While group B (experimental group) had rhythmical auditory stimulation (RAS) in addition with treadmill training exercise. Results of this study showed that post treatment improvement in gait parameters was significantly higher in the study group compared to the controls. Xin Li1, Lu Wang (2022) did a controlled study in which they enrolled 24 stroke patients with severe upper limb motor deficits. One group (n=12) was treated with combined conventional training and sensorimotor rhythm-based brain computer interference (SMR-BCI) with an audio cue, motor observation with multisensory feedback for rehabilitation of upper limb. The second group(n=12) was treated with conventional treatment only. Results of this study concluded that the first group which was treated with combined conventional and (SMR-BCI) with auditory cues, motor observation with sensory feedback might promote long lasting upper limb improvement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemiplegia
Keywords
auditory, visual, sensorimotor, hemiplegia, gait

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
28 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Rhtyhmical auditory stimulation and Visual cues (Experimental group)
Arm Type
Experimental
Arm Description
For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. For visual stimulation, white chalk will use to draw visual signals on the ground. For gait recovery, a 10-meter walkway will draw on the floor with parallel lines 2.5cm broad and 90cm long. Interline distance will maintain at 110% of the length of the initial step. Routine rehablitation treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Experimental group will be treated for 45 minutes per session, 3 days per week for 6 weeks.
Arm Title
Rhtyhmical auditory stimulation (control group)
Arm Type
Other
Arm Description
For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. Routine rehablitation treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Control group will be treated for 45 minutes per session, 3 days per week for 6 weeks.
Intervention Type
Other
Intervention Name(s)
Rhtyhmical auditory stimulation and Visual cues (Experimental group)
Intervention Description
For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. For visual stimulation, white chalk will use to draw visual signals on the ground. For gait recovery, a 10-meter walkway will draw on the floor with parallel lines 2.5cm broad and 90cm long. Interline distance will maintain at 110% of the length of the initial step. Routine recovery treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Experimental group will be treated for 45 minutes per session, 3 days per week for 6 weeks.
Intervention Type
Other
Intervention Name(s)
Rhtyhmical auditory stimulation (Control group)
Intervention Description
For auditory stimulation, walking exercises are performed on a flat floor walking path without rhythmic or musical influence. Rhythmical auditory stimulation (RAS) is produced by using Metronome App on a mobile phone. Routine recovery treatment includes a range of motion exercises for the lower extremity, passive stretching of tight muscles and conventional march exercises including marching, forward, backward and sideways walking. Control group will be treated for 45 minutes per session, 3 days per week for 6 weeks.
Primary Outcome Measure Information:
Title
Fugl-Meyer Assessment FMA (LE)
Description
FMA is used to assess sensorimotor function which consists of maximum 28 points for lower extremity and 6 points for speed and coordination. The total summed score of 34 points indicates normal function. Higher the score more is the independence.
Time Frame
Changes from baseline Fugl-Meyer Assessment FMA (LE) at 3rd week and after 6 weeks
Title
Dynamic Gait Index (DGI)
Description
DGI is composed of a total of 8 items. Total score is 24. In total, a score of less than 19/24 is predictive of falls in the elderly. A score of >22 signifies a safe ambulator.
Time Frame
Changes from baseline Dynamic Gait Index (DGI) at 3rd week and after 6 weeks
Title
Cadence
Description
Number of steps taken per unit time
Time Frame
Changes from baseline Cadence at 3rd week and after 6 weeks
Title
Gait velocity/Walking speed
Description
10 min walk test
Time Frame
Changes from baseline Gait velocity/Walking speed at 3rd week and after 6 weeks
Title
Stride length
Description
Distance between successive ground contacts of the same foot by using measuring tape.
Time Frame
Changes from baseline Stride length at 3rd week and after 6 weeks
Title
Step length
Description
Distance between successive ground contact of the opposite foot by using measuring tape.
Time Frame
Changes from baseline Step length at 3rd week and after 6 weeks
Title
Step width
Description
Transverse linear distance between two successive feet from the centers of heels by using measuring tape.
Time Frame
Changes from baseline Step width at 3rd week and after 6 weeks
Title
Step length symmetry ratio
Description
It will be calculated by dividing step length of paretic limb to non-paretic limb.
Time Frame
Changes from baseline Step length symmetry ratio at 3rd week and after 6 weeks
Title
Stride length symmetry ratio
Description
It will be calculated by dividing the stride length of paretic limb to non-paretic limb.
Time Frame
Changes from baseline Stride length symmetry ratio at 3rd week and after 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age range between 45-65 years Both male and female genders Clinically diagnosed of stroke referred by Neuro physician Patients in the chronic stage after 6 months of stroke can walk 10 meters independently. Patients with anterior cerebral artery (ACA) and middle cerebral artery (MCA) involvement with the affected side being the dominant side Those with Brunnstrom's recovery stages 3 and 4 will take part Patients with Mini-Mental State Examination (MMS) score greater than 16. According to Modified Ashworth Scale, patients of grades 1 and 1+ will be included. Muscles that go into the spasticity include hip adductors, knee flexors and ankle plantar flexors Exclusion Criteria: Patients with dementia, depression or productive psychosis will not include. Patients having any visual or auditory impairment will be excluded. Patients with foot drop Recurrent transient ischemic attack (TIA) Patients with recurrent stroke
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Tehreem Mukhtar, PhD*
Phone
+923134715275
Email
tehreem.mukhtar@riphah.edu.pk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sehrish Naureen, MSPT-NM
Organizational Affiliation
Riphah International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Tehreem Mukhtar
City
Lahore
State/Province
Punjab
ZIP/Postal Code
54000
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Tehreem Mukhtar, PhD
Phone
+923134715275
Email
tehreem.mukhtar@riphah.edu.pk

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Effects of Auditory and Visual Cueing on Sensorimotor Recovery and Gait in Hemiplegia

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