- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05170776
Efficacy of Adding Pilates to Postural Correction Exercise on Nerve Root Function and Electromyography Activity in Symptomatic Forward Head Posture: Randomized Controlled Trial (FHP)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Forward head posture (FHP) is nowadays the most common postural problem. In FHP, the head protrudes forward from the sagittal plane and appears to be positioned in front of the body, and this condition is considered the most common postural deformity. The prevalence of anterior head translation in neck pain patients was found to be 37%, out of which 58% were females and 42%were males. FHP is among the most common abnormal postures in upper quarter. 85% of patients with myofascial pain syndrome have FHP. Even more alarming is how frequently these problems are seen in younger populations since it's suggested that problems at a young age may lead to more serious consequences later in life. Pilate's method is a physical fitness system that was developed during the First World War in the early 20th century by Joseph Hubertus Pilates. Direction Control and Range Control exercises are two key types of specific exercises that should be used when specific uncontrolled movements are found. Pilates is a mind-body exercise that focuses on strength, core stability, flexibility, muscle control, posture and breathing. Exercises can be mat-based or involve use of specialized equipment. Six major components of Pilates as: Centering, Concentration, Control, Precision, Flow and Breathing.
pilates exercise and postural correction play a major role in restoring the normal posture in patients with forward head posture so this trial will be conducted to investigate efficacy of adding Pilates to postural correction exercise on nerve root function and electromyography activity in symptomatic forward head posture.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Giza, Egypt, 12511
- Al Shaymaa Shaaban Abd El Azeim
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Ages from 20-45 years old with symptomatic forward head posture will be included in this study
- Participants have FHP if CVA ≤ 50 Non- athletes
- Normal body mass index (BMI) (18- 24.9). (BMI = body mass in kg divided by subject height in meters).
Exclusion Criteria:
- any spinal problems
- Temporomandibular disease
- Participants with experience in pilates and who will not be sedentary were excluded from the study
- Previous surgery in the neck and shoulder
- neurological symptoms of the upper extremities during screening tests (e.g., Spurling test and upper limb tension tests)
- red flags suggesting of cancer, infection, vascular insufficiency
- Cervical radiculopathy or mylopathy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: DOUBLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Pilates and postural correction exercise
pilates and postural correction exercise will be received three times a week for 10 weeks
|
ten exercises will be performed:
1-Strengthening deep cervical flexors 2-Stretching cervical extensors 3- Strengthen shoulder retractors 4-Unilateral and bilateral pectoralis stretch |
|
ACTIVE_COMPARATOR: Pilates exercises
pilates exercise will be received three times a week for 10 weeks
|
ten exercises will be performed:
|
|
ACTIVE_COMPARATOR: postural correction exercises
postural corrections exercise will be received three times a week for 10 weeks
|
postural correction exercise in the form of :
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
nerve root function
Time Frame: up to ten weeks
|
nerve root function in the form of somatosensory evoked potential will be measure by electromyograph.
|
up to ten weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
pain intensity
Time Frame: up to ten weeks
|
pain intensity will be measure by visual analogue scale.
|
up to ten weeks
|
|
neck disability
Time Frame: up to ten weeks
|
neck disability will be measure by Arabic neck disability index
|
up to ten weeks
|
|
flexion and extension endurance test
Time Frame: up to ten weeks
|
the endurance will be measured by stop watch
|
up to ten weeks
|
|
muscle amplitude
Time Frame: up to ten weeks
|
electromyography will be used to measure the muscle amplitude in the form of root mean square
|
up to ten weeks
|
|
craniovertebral angle
Time Frame: up to ten weeks
|
craniovertebrel angle will be measured by surgimap program
|
up to ten weeks
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- p.t.REC/012/003411
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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