NCT06732765 Comparative Effects of Eloda With/Without Muscle Energy Technique in Patient With Quadratus Lumborum Syndrome
| NCT ID | NCT06732765 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Riphah International University |
| Condition | Rounded Shoulder Posture |
| Study Type | INTERVENTIONAL |
| Enrollment | 62 participants |
| Start Date | 2024-02-04 |
| Primary Completion | 2024-12-07 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 62 participants in total. It began in 2024-02-04 with a primary completion date of 2024-12-07.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of the study is to compare effects Comparison of Pilate exercises with and without whole body vibration on posture, disability and pain in patients with upper cross syndrome. A randomized contro ltrial will beconductedat PESSI. Non-probability convenience sampling will be used, and 62 subjects, age 20-40 years will be allocated into two groupsby the computer generated software after meeting the inclusion criteria. Both groups will receive hot pack for 15-20 minutes and Pilate exercises perform both groups as common treatment.Group A will be treated with Pilate exercisesandGroupB will be treated with Pilate exercise with whole body vibration both groups received two sessions per week for four consecutive weeks by another well trained physical therapist. Session duration for both groups ranged from 55 minutes to 1 hour. 2 sessions for 4 weeks will be given. The outcome measures will be conducted through NPRS, NDI, RSP WAS MEASURED IN SUPINE POSITION AND THEN PML AND TSD and J APP/ software before and after 4 weeks. Data will be analyzed using SPSS software version 26.After assessing normality of data by kolmo-grove test, it will be decided either parametric or non-parametric test will be used within a group or between two groups. Data will be collected at baseline and after 4 weeks of follow up.
Eligibility Criteria
Inclusion Criteria: * Age group between 18 to 45 years * Both gender male and female * individuals with mechanical lower back pain * active trigger point in the quadratus lumborum muscle * No previous history of accidents Exclusion Criteria: * Acute muscular injuries * localized or systemic infections * lumbar disc herniation * spinal abnormalities, any prior history of spinal * anticoagulant use and bleeding disorders * psychiatric conditions that would have made it difficult to provide consent
Contact & Investigator
Muhammad Salman, PhD
PRINCIPAL INVESTIGATOR
Riphah International University
Frequently Asked Questions
Who can join the NCT06732765 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, up to 45 Years, studying Rounded Shoulder Posture. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06732765 currently recruiting?
Yes, NCT06732765 is actively recruiting participants. Contact the research team at imran.amjad@riphah.edu.pk for enrollment information.
Where is the NCT06732765 trial being conducted?
This trial is being conducted at Sialkot, Pakistan.
Who is sponsoring the NCT06732765 clinical trial?
NCT06732765 is sponsored by Riphah International University. The principal investigator is Muhammad Salman, PhD at Riphah International University. The trial plans to enroll 62 participants.