Comparative Impact of RAST and TST for Improving Motor Functions in Stroke Patients

January 5, 2025 updated by: Muhammad Naveed Babur, Superior University

Comparative Impact of Rhythmic Auditory Stimulation Therapy and Task Specific Training for Improving Motor Functions in Stroke Patients

This study evaluates the effectiveness of Rhythmic Auditory Stimulation (RAS) therapy versus Task-Specific Training (TST) in enhancing motor function recovery in stroke patients. RAS uses rhythmic cues to aid movement synchronization, while TST focuses on practicing daily tasks to improve functional ability. In a randomized clinical trial, participants were assigned to either RAS or TST groups, with both receiving structured sessions over several weeks.

Study Overview

Study Type

Interventional

Enrollment (Actual)

40

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan
        • Azra Naheed Medical College, Superior University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Male and female patients diagnosed with stroke
  • Age 40-80 years (46)
  • Patients having first ever stroke occurrence
  • Moderate motor function impairments (47)
  • Patients able to follow instruction

Exclusion Criteria:

  • Patients with severe motor impairments
  • Patients who had cognitive impairments
  • Patients having other neurological conditions and musculoskeletal disorders
  • Patients having history of surgery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Health Services Research
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Rhythmic Auditory Stimulation Therapy
Rhythmic auditory stimulation (RAS) is a therapeutic technique that uses rhythmic auditory cues, like a metronome or music, to improve motor control and coordination. It is often used in rehabilitation for conditions such as stroke, Parkinson's disease, and other movement disorders to enhance gait and other motor functions through the synchronization of movements to auditory rhythms.
Experimental: Task-Specific Training
Task-specific training is a rehabilitation approach that involves practicing specific tasks or activities to improve the performance of those tasks. It is based on the principle that repetitive practice of functional tasks enhances neuroplasticity, leading to better motor skills and functional recovery, especially in stroke and neurological rehabilitation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Modified Barthel index
Time Frame: 12 Months
The Modified Barthel Index (MBI) is a crucial tool for assessing functional independence in activities of daily living (ADLs) among patients, particularly those recovering from stroke or other debilitating conditions. It evaluates 10 key self-care and mobility tasks, including feeding, bathing, grooming, dressing, and mobility. Each task is scored based on the level of assistance required, with total scores ranging from 0 (complete dependence) to 100 (complete independence). Higher scores indicate greater independence.
12 Months
Goniometer
Time Frame: 12 Months
A goniometer is an instrument used to measure the angle of joints in the body, typically to assess the range of motion (ROM). It is commonly used in physical therapy, rehabilitation, and orthopedics to evaluate joint function and monitor progress in patients recovering from injury or surgery. Range of motions of upper limb measured through this goniometer."
12 Months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 15, 2024

Primary Completion (Actual)

July 1, 2024

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

December 26, 2024

First Submitted That Met QC Criteria

January 5, 2025

First Posted (Actual)

March 25, 2025

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 5, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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