- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05069181
Pilates Mat Versus Cervical Stabilization Exercises on Myoelectric Activity of Cervical Muscles in Forward Head Posture (FHP)
Pilates Mat Versus Cervical Stabilization Exercises on Myoelectric Activity of Cervical Muscles, Craniovertebral Angle, Pain and Function in Young Adults With Forward Head Posture: Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Giza, Egypt, 12511
- Faculty of Physical Therapy-Cairo University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Subjects of both genders aged 18-25 years old with forward head posture will be included in this study
- Subjects have forward head posture if craniovertebral angle ≤ 50.
- Subjects complain non- specific neck pain for at least 3 months or at least two episodes of non-specific neck pain during the last three months.
- Normal body mass index
Exclusion Criteria:
- Subjects with any spinal problems
- Subjects with experience in Pilates exercises through the last 3 months of the start of intervention will be excluded from the study
- Previous surgery in the neck and shoulder regions
- Current participation in a structured exercises program
- 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 myelopathy
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Pilates mat exercises
one hour Pilates exercises with 10 min warm up and 5-10 min cooling down
|
Pilates mat exercises: Each Pilates session will last for one hour and commence with a 10 minute warm up and finish with a 10 min cool down. The subjects will be taught the 5 key elements of Pilates (lateral costal breathing, centring which is a neutral position of the lumbar spine with activation of the core muscles, ribcage placement, shoulder blade placement and neutral position of the cervical spine with slight upper cervical flexion at the cranio-cervical junction). Pilates exercise program will consist of warm up exercises, main treatment program (10 level) and cooling down exercises.
10 min hot pack on cervical area range of motion exercises and isometric neck exercises as a home program 3 days/week for 12 weeks
|
|
Experimental: cervical stabilization exercises
training of deep cervical flexor muscles with pressure biofeedback unit
|
10 min hot pack on cervical area range of motion exercises and isometric neck exercises as a home program 3 days/week for 12 weeks
training of deep cervical flexor muscles with pressure biofeedback unit, 20 min/day, 3 days/week for 12 weeks.
|
|
Active Comparator: conventional physiotherapy
10 min hot pack on cervical area range of motion exercises and isometric neck exercises as a home program
|
10 min hot pack on cervical area range of motion exercises and isometric neck exercises as a home program 3 days/week for 12 weeks
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Myoelectric activity of cervical muscles
Time Frame: up to twelve weeks
|
by surface electromyography (EMG)
|
up to twelve weeks
|
|
Craniocervical angle
Time Frame: up to twelve weeks
|
by photogrammetric method.
|
up to twelve weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain intensity of neck area
Time Frame: up to twelve weeks
|
by visual analogue scale 10 cm line with 2 ends, 0 and 10 ends 0 end means no pain 10 end means the worst pain
|
up to twelve weeks
|
|
function of daily life
Time Frame: up to twelve weeks
|
by neck disability index
|
up to twelve weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Haytham M Elhafez, Professor, professor of physical therapy- cairo university
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
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/003349
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- Study Protocol
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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