Viewing Study NCT06309849



Ignite Creation Date: 2024-05-06 @ 8:15 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06309849
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-08
First Post: 2024-02-10

Brief Title: Efficacy of Physical Therapy Intervention in Cervical Angina Patients at Jerash University Office Employees Randomized Clinical Trail
Sponsor: South Valley University
Organization: South Valley University

Study Overview

Official Title: Efficacy of Physical Therapy Intervention in Cervical Angina Patients at Jerash University Office Employees Randomized Clinical Trail
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
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: Cervicogenic angina CA is defined as paroxysmal angina- like pain that originates from the disorders of the cervical spine or other neck structures Because CA mimics typical cardiac angina symptoms in the elderly with cervical spondylosis are more frequently misdiagnosed Nakajima H 2006 Patients with CA may have suffered symptoms for longer periods of time and seen several clinicians due to conflicting cardiac exams Clinicians and patients are unaware that CA symptoms are stemming from cervical spine disorders However the mechanism of pain occurrence in patients with CA remains unclear
Detailed Description: Randomized Control Trail RCT will be used in the study Participants will be divided into two groups experimental and control groups Each group will include 30 participants

The study population will be employees working in JU from different departments

A total of 60 participants will be included in the study Their weight ranged from 50 kilograms to 100 kilograms And their height ranged from 150 centimeters to 190 centimeters And their body mass index ranged from 222 to 277 This will be divided into 2 groups with 30 participants in each group

The data collected will focus on measuring the Range of Motion ROM of the cervical spine using an Electro-Goniometer the pain using Visual Analogue Scale VAS and the Hart Rate HR using an electro cardio Graphic ECG

The study setting will be JU located in Jerash City Jordan

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