Effect of Thoracic Manual Therapy in Hemiplegic Patients

NCT ID: NCT04503499

Last Updated: 2023-11-03

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

47 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-09-15

Study Completion Date

2019-08-15

Brief Summary

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Neurological problems both lead to many respiratory problems primarily and events secondary to neurological diseases or symptoms can be the cause of respiratory failure. The addition of respiratory failure will adversely affect the course of the neurological picture, making treatment more difficult.

The cardiopulmonary functions of hemiplegia patients decrease due to the decrease in the expansion of the thoracic part on the hemiplegic side and insufficient respiratory muscles. In addition, common symptoms in stroke patients, including limited use of ankylosis and muscle movements, cause oxygen deficiency and increased metabolic demands. After stroke, thoracic expansion is reduced upon paralysis of the diaphragm and respiratory muscles. Continuation of this condition can lead to muscle fibrosis. As a result, the level of thoracic expansion decreases during breathing.

A decrease in thoracic spine mobility correlates with a decrease in forced vital capacity (FVC) and forced expiratory volume in the first second (FEV1). The increase in the rigidity of the chest wall affects the ventilator pumping mechanism, reducing the level of rigidity (increasing the mobility of the chest wall) is recommended as a way to improve lung function.

Detailed Description

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Conditions

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Stroke

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

SINGLE

Participants

Study Groups

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Study Group

The group to which the manuel therapy will be applied.

Group Type EXPERIMENTAL

Manuel Therapy

Intervention Type OTHER

The manual therapy protocol will consist of 45-60 minutes and the following techniques;

* suboccipital decompression
* cervical mobilization (in the posterior-anterior direction)
* sternocleidomastoid release
* scalene release
* trapezoidal release
* scalene release
* pectoralis tractus
* sternoclavicular joint mobilization
* sternum mobilization
* parasternal circumference intercostal and paravertebral release
* diaphragm release
* rib reasing
* scapulothoracic joint mobilization
* thoracic vertebra mobilization

Myofascial release techniques will be applied for 3-5 minutes each.

Mobilization techniques were applied in each joint for 30 seconds and 5 times.

Control Group

The control group where only the evaluations will be made.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Manuel Therapy

The manual therapy protocol will consist of 45-60 minutes and the following techniques;

* suboccipital decompression
* cervical mobilization (in the posterior-anterior direction)
* sternocleidomastoid release
* scalene release
* trapezoidal release
* scalene release
* pectoralis tractus
* sternoclavicular joint mobilization
* sternum mobilization
* parasternal circumference intercostal and paravertebral release
* diaphragm release
* rib reasing
* scapulothoracic joint mobilization
* thoracic vertebra mobilization

Myofascial release techniques will be applied for 3-5 minutes each.

Mobilization techniques were applied in each joint for 30 seconds and 5 times.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Being between 45-65 years old
* Stage 4-6 according to Brunnstrom
* According to Modified Ashworth, the upper extremity is at most two values
* Sufficient to answer the level of consciousness survey
* No smoking
* No hearing or vision loss

Exclusion Criteria

* Not being able to read and write
* Having cognitive impairment
* Hearing difficulties and vision loss
* Having any acute pain
* Acute Bronchitis
Minimum Eligible Age

45 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Istinye University

OTHER

Sponsor Role lead

Responsible Party

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Yasemin Çırak

Physiotherapist, PhD, Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Istanbul Okan University

Istanbul, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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0002

Identifier Type: -

Identifier Source: org_study_id

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