Immediate Effect of One-session MRT in Hemiparetics

NCT ID: NCT05062746

Last Updated: 2022-01-27

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

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-10

Study Completion Date

2022-01-16

Brief Summary

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

Detailed Description

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Conditions

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Hemiparesis;Poststroke/CVA Satisfaction, Patient

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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MRT group

One session Matrix-Rhythm Therapy

Group Type EXPERIMENTAL

Matrix-Rhythm Therapy

Intervention Type OTHER

One session Matrix-Rhythm Therapy will be applied to affected body parts.

Control group

One session routine, conventional physiotherapy and rehabilitation

Group Type OTHER

Conventional physiotherapy and rehabilitation

Intervention Type OTHER

Hemiparetics wil receive one session conventional physiotherapy and rehabilitation.

Interventions

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Matrix-Rhythm Therapy

One session Matrix-Rhythm Therapy will be applied to affected body parts.

Intervention Type OTHER

Conventional physiotherapy and rehabilitation

Hemiparetics wil receive one session conventional physiotherapy and rehabilitation.

Intervention Type OTHER

Eligibility Criteria

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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.
Minimum Eligible Age

30 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pamukkale University

OTHER

Sponsor Role lead

Responsible Party

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Ayşe Ünal

PT.,PhD

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Pamukkale University

Denizli, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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22.09.2021-MRT

Identifier Type: -

Identifier Source: org_study_id

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