- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06738238
Comparative Effects of Eldova Technique and Corrective Exercises in Upper Cross Syndrome
To Compare Effects of Eldova Technique and Corrective Exercises in Upper Cross Syndrome
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
KPK
-
Peshawar, KPK, Pakistan, 25000
- Madina colony
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male and Female subjects
- Age between 15 to 35 years
- Subjects with scapular dyskinesia
- Subject with rounded shoulders
Exclusion Criteria:
- Subjects with cervical discogenic pain
- Subjects with spinal stenosis
- Cervical spine surgery
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Eldova
Elongation Longitudinaux Avec Decoaption Osteo Articulaire
|
In this, each position will be maintained for 1 minute Level: C0/C1/C2 The patient is side lying with bottom arm folded under the head and maintain the neck in a horizontal position with the spine. the bottom leg is bent to stabilize the torso in a vertical position. Level: C4/C5 Patient lying in supine position and raise both hand arm towards the roof of the room with extended wrist. Bilateral knee to chest with planter flexion at ankle joint. Level: C5/C6 Same position as for c4/c5 with the arms will be elevated 120 degree Level C6/C7 Supine position with one arm abducted 90 degree and wrist joint at extension and the other hand abducted 30degrees with wrist joint at extension and one leg knee to chest and one leg raise with knee extension and planter flexion at ankle joint. Level: T4/T5 Quadruped position with one arm abducted 90degrees with wrist at extension Level: T6/T7. Conventional TX is Hot Pack, Tens for 10min. Patient is assessed through baseline, week 1, week 2 and week 4. |
|
Experimental: Corrective exercises
corrective exercises
|
In this, each position will be maintained for 1 minute Level: C0/C1/C2 The patient is side lying with bottom arm folded under the head and maintain the neck in a horizontal position with the spine. the bottom leg is bent to stabilize the torso in a vertical position. Level: C4/C5 Patient lying in supine position and raise both hand arm towards the roof of the room with extended wrist. Bilateral knee to chest with planter flexion at ankle joint. Level: C5/C6 Same position as for c4/c5 with the arms will be elevated 120 degree Level C6/C7 Supine position with one arm abducted 90 degree and wrist joint at extension and the other hand abducted 30degrees with wrist joint at extension and one leg knee to chest and one leg raise with knee extension and planter flexion at ankle joint. Level: T4/T5 Quadruped position with one arm abducted 90degrees with wrist at extension Level: T6/T7. Conventional TX is Hot Pack, Tens for 10min. Patient is assessed through baseline, week 1, week 2 and week 4.
All position will be held for 10 seconds.
Initial phase Duration of this phase is 2 weeks.
Exercise 1: lying supine on a foam roll with different abduction angles Exercise 2: side lying with external rotation Exercise 3: side lying with forward flexion Exercise 4: standing diagonal flexion Exercise 5: military press Improvement phase.
Duration of this phase is 1 week we only add thera- band and dumbbells to the previously mentioned exercises Exercise 1: side lying external rotation with dumbbell Exercise 2: side lying forward flexion with dumbbell Exercise 3: standing diagonal flexion with thera-band Exercise 4: standing external rotation with thera band.
Exercise 5: abduction in sitting on training ball.
Exercise 6: lying prone on foam ball with different abduction angles Maintenance phase.
Duration of this phase is 1 week.
Conventional treatment Hot Pack, Tens for 10 minutes Patient is assessed through baseline, week 1, week 2 and week 4.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Lateral scapular slide test.
Time Frame: 4 weeks
|
The scapular position is measured by taking the side to side differences between both sides in all 3 test positions. The measurements are taken from the inferior angle of the scapulae to the spinous process of the thoracic vertebrae on horizontal plane. The test is done in 3 positions, with the arm abducted to 0, 45 and 90 degrees in the coronal plane. Position 1 involves placing the shoulder in neutral position, with the arms relaxed at the sides, Position 2 the humerus is placed in medial rotation and 45degree abduction, by positioning patients hands around the waist, Position 3 the humerus is placed in maximal rotation and 90degree abduction. The Test is positive when there is a difference of 1.5 cm when measurements are compared bilaterally. |
4 weeks
|
|
Forward head posture (tragus to wall)
Time Frame: 4 weeks
|
Horizontal distance between tragus of the ear and wall, standing with heels and buttocks against the wall (to prevent pivoting), knees extended and chin.
Nine and half centimeter is normal anything greater than this value indicate FHP.
|
4 weeks
|
|
Neck pain
Time Frame: 4 weeks
|
is strongly associated with upper body dysfunction and can affect daily lives activities.
To measure neck pain before and after treatment neck disability index questionnaire will be filled from participant's neck disability index questionnaire with score of more than 20%.
|
4 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Dr. Mudassir Shah, MS-OMPT, Riphah International University
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
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
- Riphah/RCRAHS/REC/MS-PT/09136
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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