Effects of ELDOA on neck pain in Upper Cross Syndrome
Effects of ELDOA in Patients With Upper Cross Syndrome
NA · Riphah International University · NCT06564077
This study tests if the ELDOA technique can help people with Upper Cross Syndrome reduce neck pain and improve their movement and daily activities.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 20 Years to 40 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Harīpur, KPK) |
| Trial ID | NCT06564077 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the impact of the ELDOA technique on reducing neck pain, improving range of motion, and decreasing disability in patients with Upper Cross Syndrome. The study focuses on individuals suffering from muscular imbalances that lead to poor posture and associated pain. Participants will undergo the ELDOA technique combined with conventional therapy to assess its effectiveness in alleviating symptoms related to this condition. Measurements will include cervical range of motion, kyphosis, and pain levels using standardized scales.
Who should consider this trial
Good fit: Ideal candidates are individuals with forward head posture, limited cervical range of motion, kyphosis, and neck pain rated above 3 on the NPRS scale.
Not a fit: Patients with dizziness, history of surgery or fractures, severe skin sensitization, cervical radiculopathy, trauma of the upper extremity, malignancy, or scoliosis may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve the quality of life for patients suffering from neck pain due to Upper Cross Syndrome.
How similar studies have performed: While the ELDOA technique is established, the specific application for Upper Cross Syndrome is relatively novel and has not been extensively tested in similar studies.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Forward head posture (Measuring Tape used to record the tragus and wall distance in (cm) ,with considering the normative value 10 to 1055 cm in females and male respectively) * Limited cervical range of motion (Flexion: less than 80◦, Extension: less than 70◦, Rotation: less than 90◦ both sides., Lateral flexion: less than 20◦) * Kyphosis measure through flexi curve ruler * Neck Pain more than 3 on NPRS scale Exclusion Criteria: * Participants having complaints of dizziness * History of surgery or fracture * Severe skin sensitization * Cervical radiculopathy * Trauma of upper extremity * Malignancy of the upper limb or thorax * Scoliosis
Where this trial is running
Harīpur, KPK
- DHQ Hospital — Harīpur, KPK, Pakistan (RECRUITING)
Study contacts
- Principal investigator: maria Khalid, MSOMPT — Riphah International University
- Study coordinator: maria khalid, MSOMPT
- Email: maria.khalid@riphah.edu.pk
- Phone: 03315369768
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Neck Pain, Upper Cross Syndrome, ELDOA, pain