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Clinical Trials/NCT06882213
NCT06882213Enrolling By InvitationNot Applicable

Unlocking Trunk Potential After Stroke: A Novel Approach Combining Transcranial Direct Current Stimulation and Core Stability Exercise

Beni-Suef University1 site in 1 country60 target enrollmentStarted: March 29, 2025Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
60
Locations
1
Primary Endpoint
Trunk Impairment Scale (TIS).

Study Overview

Brief Summary

To evaluate the effects of the combining transcranial direct current stimulation with core stability exercises on trunk performance in poststroke hemiparetic patients, the secondary outcome is to evaluate the balance and the functional performance of the participants.

Detailed Description

This study will conduct to 60 male and female patients with post stroke hemiparesis with age ranged between 55 to 70 years, the patients will be categorized to two equal groups.

  • Group A (study group): will receive simultaneously a combination of transcranial direct current stimulation combined with core stability exercise.
  • Group B (control group): will receive core stability exercise. All patients will be assessed for trunk performance, balance, and functional performance before and after interventions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
55 Years to 75 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients will be included if they are ≥ 55 years old of both sex, had a first-time right or left stroke within the preceding six months that damaged the cerebral cortex verified by (computed tomography or MRI report, neurological examination, and medical chart).
  • •Patients can stand and walk independently.
  • •Modified Ashworth Scale (MAS) of upper limb muscle ≤ 1+.
  • •All the patients received a conventional physiotherapy program in the acute stage and post-discharge from the hospital.
  • •None of the patients participated in any other study or placebo

Exclusion Criteria

  • •Patients with neurological or orthopedic problems, paralysis neglect, behavioral abnormalities, dementia any shoulder dysfunction before or post-stroke (dislocation or subluxation), or those who using upper limb splints.
  • •Recurrent strokes or hemiparesis due to other neurological causes rather than stroke eg .(Brain tumor).
  • •Obesity (BMI ≥ 30 kg/m2).

Arms & Interventions

Control group

Active Comparator

will receive core stability exercise.

Intervention: core stability exercise. (Other)

Study Group

Active Comparator

will receive simultaneously a combination of transcranial direct current stimulation combined with core stability exercise.

Intervention: transcranial direct current stimulation (Other)

Study Group

Active Comparator

will receive simultaneously a combination of transcranial direct current stimulation combined with core stability exercise.

Intervention: core stability exercise. (Other)

Outcomes

Primary Outcomes

Trunk Impairment Scale (TIS).

Time Frame: up to 8 weeks

trunk performance will be assessed by Trunk Impairment Scale (TIS).

Berg Balance Scale

Time Frame: up to 8 weeks

Balance will be assessed by berg balance scale, the balance score ranges from 0 to 56, with lower scores indicating increased risk of balance loss and higher scores indicating improved functional mobility. Time up and go test (TUG)n Score \< 10 seconds = normal \< 20 seconds = good mobility; can walk outside alone; does not require a walking aid \< 30 seconds = walking and balance problems; cannot walk outside alone; requires walking aid

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mohammed Youssef Elhamrawy

Lecturer of Physical therapy

Beni-Suef University

Study Sites (1)

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