Effects of Sensory Stimulation Versus Sensorimotor Therapy on Spasticity, Motor Function and Daily Activities in Stroke

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

42 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-01

Study Completion Date

2024-09-01

Brief Summary

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To compare effects of exteroceptive and proprioceptive sensory stimulation versus sensorimotor therapy on spasticity, motor function and activities of daily living in patients with stroke

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Detailed Description

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It will be a randomized clinical trial in which total 42 stroke patients will be recruited through non probability convenience sampling techniques. Data will be collected from Gujranwala Medical College Teaching Hospital and Riphah Rehabilitation Center Lahore. The patients who are fulfilling the inclusion criteria will be randomly assigned to either group A (n=21) which will receive intervention exteroceptive and proprioceptive sensory stimulation or to group B (n=21) which will receive sensorimotor therapy for 50 minutes per session, 03 times a week, for 06 weeks. Baseline treatment will be given to both groups. Conventional therapy will be given for 20 minutes per session, 03 times a week, for 06 weeks. Data collection tools will be Fugl-Meyer Assessment, Modified Barthel Index and Modified Ashworth Scale.

Conditions

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Stroke, Ischemic Proprioceptive Disorders Sensory Defect

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients will be divided to group A (n=21) which will receive intervention exteroceptive and proprioceptive sensory stimulation and to group B (n=21) which will receive sensorimotor therapy for 50 minutes per session, 03 times a week, for 06 weeks .

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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exteroceptive and proprioceptive sensory stimulation

Patients in this group will receive exteroceptive and proprioceptive sensory stimulation

Group Type EXPERIMENTAL

exteroceptive and proprioceptive sensory stimulation training

Intervention Type OTHER

Patients in this group will receive intervention exteroceptive and proprioceptive sensory stimulation for 50 minutes per session, 03 times a week, for 06 weeks

sensorimotor therapy group

Patients in this group will receive sensorimotor therapy

Group Type ACTIVE_COMPARATOR

sensorimotor therapy group

Intervention Type OTHER

Patients will receive sensorimotor therapy for 50 minutes per session, 03 times a week, for 06 weeks

Interventions

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exteroceptive and proprioceptive sensory stimulation training

Patients in this group will receive intervention exteroceptive and proprioceptive sensory stimulation for 50 minutes per session, 03 times a week, for 06 weeks

Intervention Type OTHER

sensorimotor therapy group

Patients will receive sensorimotor therapy for 50 minutes per session, 03 times a week, for 06 weeks

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The patients with chronic stroke (6 months to 2 years)
* Patient 's muscular activity on Stage 3 or higher according to the Brunnstrom's stages of stroke recovery.
* Patients having Mini Mental State Examination score \> 24

Exclusion Criteria

* Significant musculoskeletal impairments (e.g., arthritis, joint contractures).
* Any other neurological disorders like multiple sclerosis, Parkinson 's disease.
* History of orthopaedic surgery.
* Unstable medical conditions (e.g., uncontrolled hypertension, cardiovascular disease).
* Severe visual or vestibular impairments.
* Lower limb prosthesis.

Minimum Eligible Age

50 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No