Efficacy of Adding Pilates to Postural Correction Exercise on Nerve Root Function and Electromyography Activity in Symptomatic Forward Head Posture: Randomized Controlled Trial (FHP)

August 5, 2022 updated by: Al Shaymaa Shaaban Abd El Azeim, Cairo University
to investigate the Efficacy of adding Pilates to postural correction exercise on nerve root function and electromyography activity in symptomatic forward head posture: Randomized Controlled Trial

Study Overview

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

Interventional

Enrollment (Actual)

120

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Giza, Egypt, 12511
        • Al Shaymaa Shaaban Abd El Azeim

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 45 years (ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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. Hip Twist Level 1
  2. Double leg stretch Level 1
  3. Double leg stretch Level 2
  4. One leg stretch Level 1
  5. Clam Level 1
  6. Scissors Level 1
  7. Arm openings Level 1
  8. Breast stroke prep Level 1t
  9. Hip Twist Level 1.
  10. Breast stroke prep Level 2 as for level 1 postural correction exercise

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:

  1. Hip Twist Level 1
  2. Double leg stretch Level 1
  3. Double leg stretch Level 2
  4. One leg stretch Level 1
  5. Clam Level 1
  6. Scissors Level 1
  7. Arm openings Level 1
  8. Breast stroke prep Level 1t
  9. Hip Twist Level 1.
  10. Breast stroke prep Level 2 as for level 1
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 :

  1. Strengthening deep cervical flexors through chin tucks,
  2. Stretching cervical extensors through a chin drop
  3. Strengthen shoulder retractors
  4. Unilateral and bilateral pectoralis stretch alternating each two-week period.

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

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

January 1, 2022

Primary Completion (ACTUAL)

June 1, 2022

Study Completion (ACTUAL)

June 1, 2022

Study Registration Dates

First Submitted

December 11, 2021

First Submitted That Met QC Criteria

December 11, 2021

First Posted (ACTUAL)

December 28, 2021

Study Record Updates

Last Update Posted (ACTUAL)

August 9, 2022

Last Update Submitted That Met QC Criteria

August 5, 2022

Last Verified

August 1, 2022

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

No

Studies a U.S. FDA-regulated device product

No

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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