Viewing Study NCT06460532



Ignite Creation Date: 2024-06-16 @ 11:52 AM
Last Modification Date: 2024-10-26 @ 3:32 PM
Study NCT ID: NCT06460532
Status: COMPLETED
Last Update Posted: 2024-06-14
First Post: 2024-06-11

Brief Title: Effects of Diaphragm Manual Therapy Verses Sustained Natural Apophyseal Glide in Mechanical Neck Pain
Sponsor: Riphah International University
Organization: Riphah International University

Study Overview

Official Title: Effects of Diaphragm Manual Therapy Versus Sustained Natural Apophyseal Glide on Pain Range of Motion and Functional Disability in Patients With Mechanical Neck Pain
Status: COMPLETED
Status Verified Date: 2024-10
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: Mechanical neck pain is defined as pain and discomfort localized between the superior nuchal line cervical spine and the spinous process of the first thoracic vertebra Some of the most typical factors include continuous use of mobile phones and computers working in sedentary jobs etc Study aimed to compare diaphragm manual therapy and Sustained Natural Apophyseal Glide on pain range of motion and functional disability in patients with mechanical neck pain
Detailed Description: This project will be a Randomized Clinical Trial conducted to check the effects of Diaphragm manual therapy versus sustained natural apophyseal glide on pain range of motion and functional disability in patients with mechanical neck pain at Sehat Medical Complex Lahore through non-probability convenient sampling technique on 34 patients will be allocated using simple random sampling through Computer generated Randomization into Group A and Group B Group A will be treated with Diaphragm Manual Therapy and baseline treatment was given and Group B with Sustained Natural Apophyseal Glide and baseline treatment was given All Exercise were performed 3 times a week for total 4 weeks Outcome measures will be conducted through NPRS for pain ROM measured by Goniometer and Neck Disability Index NDI for Disability after 4 weeks Data was analyzed during SPSS software version 25 After assessing the normality of data by the Shapiro-Wilk test it decided whether either parametric or non-parametric tests were used within a group or between two groups

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