NCT06738238

Brief Summary

The objective of the study is to compare the effects of ELDOA technique and corrective exercises in Upper cross syndrome. The study will be randomized control trial including two experimental groups having 42 participants in each group.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
84

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2024

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

May 1, 2024

Completed
8 months until next milestone

First Submitted

Initial submission to the registry

December 12, 2024

Completed
1 day until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 13, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 13, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 17, 2024

Completed
Last Updated

December 17, 2024

Status Verified

December 1, 2024

Enrollment Period

8 months

First QC Date

December 12, 2024

Last Update Submit

December 12, 2024

Conditions

Keywords

Upper cross syndromeELDOACorrective exercises

Outcome Measures

Primary Outcomes (3)

  • Lateral scapular slide test.

    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)

    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

    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

Study Arms (2)

Eldova

EXPERIMENTAL

Elongation Longitudinaux Avec Decoaption Osteo Articulaire

Other: ELDOA

Corrective exercises

EXPERIMENTAL

corrective exercises

Other: ELDOAOther: CORRECTIVE EXERCISES

Interventions

ELDOAOTHER

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.

Corrective exercisesEldova

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.

Corrective exercises

Eligibility Criteria

Age15 Years - 35 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Male and Female subjects
  • Age between 15 to 35 years
  • Subjects with scapular dyskinesia
  • Subject with rounded shoulders

You may not qualify if:

  • Subjects with cervical discogenic pain
  • Subjects with spinal stenosis
  • Cervical spine surgery

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Madina colony

Peshawar, KPK, 25000, Pakistan

Location

Related Links

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type Preus

Study Officials

  • Dr. Mudassir Shah, MS-OMPT

    Riphah International University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 12, 2024

First Posted

December 17, 2024

Study Start

May 1, 2024

Primary Completion

December 13, 2024

Study Completion

December 13, 2024

Last Updated

December 17, 2024

Record last verified: 2024-12

Data Sharing

IPD Sharing
Will not share

Locations