Immediate Effect of One-session MRT in Hemiparetics

January 26, 2022 updated by: AYŞE ÜNAL, Pamukkale University

Immediate Effect of One-session Matrix Rhythm Therapy on the Functional Status and Treatment Satisfaction of Hemiparetic Patients

Immediate effect of one-session Matrix Rhythm Therapy on the functional status and treatment satisfaction of hemiparetic patients will be investigated.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Interventional

Enrollment (Actual)

38

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

  • Turkey
      • Denizli, Turkey
        • Pamukkale 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

30 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • to have single-sided hemiparesis for the first time,
  • to have hemiparesis at least four weeks earlier,
  • to have Modified Rankin Score of ≤3

Exclusion Criteria:

  • to use a cardiac pacemaker,
  • to have communication problems,
  • to have other neurological, psychiatric and/or orthopedic problems other than hemiparesis.

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: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: SINGLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: MRT group
One session Matrix-Rhythm Therapy
Other: Matrix-Rhythm Therapy
One session Matrix-Rhythm Therapy will be applied to affected body parts.
OTHER: Control group
One session routine, conventional physiotherapy and rehabilitation
Other: Conventional physiotherapy and rehabilitation
Hemiparetics wil receive one session conventional physiotherapy and rehabilitation.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Motricity Motor Scale
Time Frame: 5 minutes
Index for motor impairment after stroke
5 minutes
Trunk Impairment Scale
Time Frame: 10 minutes
It consists of 3 subscales of static and dynamic sitting balance and trunk coordination
10 minutes
The Box and Block Test
Time Frame: 2 minutes
The Box and Block Test (BBT) measures unilateral gross manual dexterity. It is a quick, simple and inexpensive test. It can be used with a wide range of populations, including clients with stroke.
2 minutes
The Nine-Hole Peg Test
Time Frame: 2 minutes
The Nine-Hole Peg Test (9HPT) is used to measure finger dexterity in patients with various neurological diagnoses. Administered by asking the client to take the pegs from a container, one by one, and place them into the holes on the board, as quickly as possible.
2 minutes
Treatment Satisfaction Scale
Time Frame: 30 sec.
The amount of satisfaction that a patient feels ranges across a continuum from none (0) to an extreme amount of satisfaction (10).
30 sec.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Global Rating of Change Scale
Time Frame: 30 sec.
Global Rating of Change (GRC) scales provide a means of measuring self-perceived change in health status.
30 sec.

Collaborators and Investigators

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

Sponsor

Pamukkale University

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)

September 10, 2021

Primary Completion (ACTUAL)

December 15, 2021

Study Completion (ACTUAL)

January 16, 2022

Study Registration Dates

First Submitted

September 22, 2021

First Submitted That Met QC Criteria

September 22, 2021

First Posted (ACTUAL)

September 30, 2021

Study Record Updates

Last Update Posted (ACTUAL)

January 27, 2022

Last Update Submitted That Met QC Criteria

January 26, 2022

Last Verified

January 1, 2022

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 22.09.2021-MRT

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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