Effects of Upper Cervical Manual Therapy on Obliquus Capitis Inferior Muscle Morphology
This study aims to evaluate the effects of upper cervical manual therapy on the morphology of your Obliquus Capitis Inferior muscle, specifically measuring changes in its length and width using musculoskeletal ultrasound.
Single Thrust for Neck Joint Adjustment
+ Single Thrust for Neck Joint Adjustment
Neurologic Manifestations+2
+ Pain
+ Signs and Symptoms
Treatment Study
Summary
Study start date: May 1, 2025
Actual date on which the first participant was enrolled.This study focuses on understanding the immediate impacts of two different upper neck manual therapy techniques. It involves individuals receiving these therapies and examines specific aspects related to neck posture and muscle health. The research aims to improve understanding of how these therapies affect the Obliquus Capitis Inferior, a muscle located at the base of the skull, which is often associated with neck pain and discomfort. The findings could potentially enhance treatment strategies for conditions related to neck pain and posture. During the study, participants receive one of the two manual therapies. The effects of these therapies are then measured using musculoskeletal ultrasound, a safe and non-invasive imaging technique. This technique helps assess changes in the length and width of the Obliquus Capitis Inferior muscle. The study also evaluates the craniovertebral angle, a measure of neck posture, and the perceived position of the atlas, the topmost vertebra of the spine.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.80 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 65 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ShamStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Florida Gulf Coast University Marieb Hall 101
Fort Myers, United StatesOpen Florida Gulf Coast University Marieb Hall 101 in Google Maps