Viewing Study NCT04503499



Ignite Creation Date: 2024-05-06 @ 3:02 PM
Last Modification Date: 2024-10-26 @ 1:42 PM
Study NCT ID: NCT04503499
Status: COMPLETED
Last Update Posted: 2023-11-03
First Post: 2020-07-28

Brief Title: Effect of Thoracic Manual Therapy in Hemiplegic Patients
Sponsor: Istinye University
Organization: Istinye University

Study Overview

Official Title: Acute Effect of Thoracic Manual Therapy on Respiratory Capacity in Hemiplegic Patients
Status: COMPLETED
Status Verified Date: 2023-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: 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: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None