Skip to main content
Clinical Trials/CTRI/2025/05/087288
CTRI/2025/05/087288Not yet recruitingNot Applicable

A Study to compare Additive Effect of Electromyographic Biofeedback vs Conventional Treatment on Spasticity and Upper Limb Motor Function in Subacute Stroke Subjects with Wrist and Hand Dysfunction – A Comparative Study

Vishwa Bengali1 site in 1 country30 target enrollmentStarted: January 7, 2025Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
30
Locations
1
Primary Endpoint
The primary outcome is Spasticity and upper limb motor function, which will be assessed pre-test and post-test.

Study Overview

Brief Summary

Stroke is a sudden loss of neurological functions. It can be either an ischemic or hemorrhagic type of stroke. The subjects suffering from stroke have various motor symptoms, out of which spasticity is one of the most common features found in the affected limb. Subjects with stroke have various treatment procedures available to deal with these problems, such as early medical interventions and rehabilitation programs and a wide range of techniques, and these approaches are used currently in rehabilitation programs. These techniques have partial effectiveness, especially for upper extremities and hand, as key role player in activities of daily living (ADL) performances. Due to the progressive increase in stroke incidence and the need for effective therapy, the effectiveness of biofeedback therapy on the hand function and activities of daily living performances in stroke survivors should be studied.

Study Design

Study Type
Interventional
Allocation
Coin toss, Lottery, toss of dice, shuffling cards etc
Masking
Not Applicable

Eligibility Criteria

Ages
40.00 Year(s) to 65.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • •Subjects with 3 to 6 months post-stroke duration.
  • •Mini mental status examination score should be less than 24 Skin intact on hemiparetic arm Medically stable.

Exclusion Criteria

  • •Modified Ashworth Scale (MAS) less than or equal to
  • •Other acute injuries to arms or hands.
  • •Intramuscular Botox injections in any upper extremity muscle in the last 3 months.
  • •Subjects with cardiac pacemakers.
  • •Stroke patients who are not cooperative.
  • •Stroke patients who have auditory and/or visual deficits.
  • •Stroke patients who do not have proper medical history .
  • •Subjects having another neurological deficit with stroke.

Outcomes

Primary Outcomes

The primary outcome is Spasticity and upper limb motor function, which will be assessed pre-test and post-test.

Time Frame: OUtcomes will be measured at baseline data and after 4 weeks of intervention.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Vishwa Bengali
Sponsor Class
Other [self]

Study Sites (1)

Loading locations...

Similar Trials