- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07573527
Effectiveness of Tele-Rehabilitation in Managing Rhomboid Trigger Points in Patients With Myofascial Pain Syndrome
Study Overview
Status
Conditions
Detailed Description
Rhomboid myofascial pain syndrome is a common yet often underreported musculoskeletal condition characterized by the presence of myofascial trigger points within the rhomboid muscles. These trigger points produce localized and referred pain, reduced range of motion, and functional limitations that can significantly affect daily activities. The condition is strongly associated with poor posture, prolonged sitting, and repetitive upper limb activities, particularly among individuals with sedentary lifestyles and high occupational demands. Evidence indicates a high prevalence of rhomboid trigger points, with many individuals experiencing moderate pain that interferes with their routine work and overall quality of life.
Biomechanically, sustained postural stress such as forward head posture and rounded shoulders increases the load on scapular stabilizing muscles, leading to muscle fatigue, microtrauma, and the development of trigger points. These changes contribute to altered scapular kinematics, muscle imbalance, and restricted movement. Self-myofascial release techniques have been shown to reduce pain sensitivity, improve circulation, and restore muscle function, making them an effective approach for managing myofascial pain.
Tele-rehabilitation has emerged as a practical and accessible method for delivering physiotherapy interventions remotely, allowing patients to perform guided exercises and self-myofascial release without the need for frequent in-person visits. This is particularly beneficial for individuals with busy schedules or limited access to healthcare services.
This randomized controlled trial aims to evaluate the effectiveness of tele-rehabilitation, incorporating self-myofascial release and exercise therapy, in reducing pain intensity, improving functional range of motion, and decreasing neck disability in patients with rhomboid trigger points associated with myofascial pain syndrome. The study also seeks to determine the feasibility of tele-rehabilitation as a convenient and sustainable alternative to conventional physiotherapy for managing rhomboid-related musculoskeletal pain.
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Maria Khalid, MSOMPT
- Phone Number: 03315369768
- Email: maria.khaild@riphah.edu.pk
Study Locations
-
-
Sindh
-
Karachi, Sindh, Pakistan
- JPMC
-
Contact:
- maria khalid, MSOMPT
- Phone Number: 03315369768
- Email: maria.khalid@riphah.edu.pk
-
Contact:
- Rameeqa Aamir, MSOMPT*
-
Principal Investigator:
- Rameeqa Aamir, MSOMPT*
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
Participants falling in this category would be recruited into the study.
- Age 18-35 years
- Both Genders: Male and Female
- Paitents experiencing Neck and upper back pain due to active trigger points.(16) According to Travell and Simons (1999)criteria, active myofascial trigger points (MTrPs) are identified.
- NPRS ≥4
- Presence of maximum one or more than one MTrPs in the Romboids muscle.
- Prolong sitting at least 6 hours per day.
- Access to a device with internet connection ( for tele rehabilitation group).
Exclusion Criteria:
Participants falling in this category would be excluded from the study.
- Participants fall in this category would be excluded of the study.
- Patients currently taking analgesics (painkillers) or muscle relaxants.
- Any inflammatory pathology, neurological impairment, and cervical tumor.
- Other deformities such as scoliosis or torticollis.
- Spinal Injuries and any other co morbidity.
- Any surgery, trauma, fracture and fall.
- Pregnancy.
- Patient unwilling to comply follow up schedule.
- Patient involvement in another interventional study.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Tele-rehabilitation (Exercise Therapy + Self-Myofascial Release)
|
|
|
Other: Conventional Myofascial Release Treatment
|
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inclinometer for functional range of motion
Time Frame: 2 weeks
|
An inclinometer is a reliable and valid instrument used to measure cervical range of motion (ROM) in flexion, extension, rotation, and lateral flexion.
It provides objective and reproducible angular measurements of spinal movement.
Studies have reported excellent intra-rater and inter-rater reliability (ICC = 0.85-0.98)
for cervical motion assessment using a dual inclinometer.
|
2 weeks
|
|
Numeric Pain Rating Scale (NPRS)
Time Frame: 2 weeks
|
The Numerical Pain Rating Scale (NPRS) is a simple, reliable, and valid tool used to assess pain intensity.
It consists of an 11-point scale ranging from 0 to 10.The NPRS shows strong construct and concurrent validity when compared with other established pain assessment tools.The NPRS has demonstrated excellent test-retest reliability (r = 0.95) is across various musculoskeletal and rehabilitation populations
|
2 weeks
|
|
Neck Disability Index (NDI)
Time Frame: 2 weeks
|
The Neck Disability Index (NDI) is a standardized questionnaire used to assess the impact of neck pain on daily activities.
It consists of 10 items, each scored from 0 to 5, with higher scores indicating greater disability.
The NDI has shown excellent reliability (ICC = 0.89-0.94)
and strong validity for evaluating functional limitations in patients with neck and upper back pain.
|
2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Maria khalid, MSOMPT, Riphah International University
Study record dates
Study Major Dates
Study Start (Estimated)
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
Keywords
Additional Relevant MeSH Terms
- Pain
- Neurologic Manifestations
- Musculoskeletal Diseases
- Muscular Diseases
- Pathological Conditions, Signs and Symptoms
- Signs and Symptoms
- Myofascial Pain Syndromes
- Neck Pain
- Health Services Administration
- Delivery of Health Care
- Therapeutics
- Patient Care
- Health Services
- Health Care Facilities Workforce and Services
- Rehabilitation
- Aftercare
- Continuity of Patient Care
- Telemedicine
- Patient Care Management
- Telerehabilitation
Other Study ID Numbers
- REC/ Rameeqa Aamir 02435
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.
Clinical Trials on Myofascial Pain Syndrome
-
Mayo ClinicNational Center for Complementary and Integrative Health (NCCIH)RecruitingMyofascial Pain | Myofascial Pain Syndrome - Lower BackUnited States
-
Lahore University of Biological and Applied SciencesNot yet recruiting
-
Medical University of SilesiaCompletedMyofascial Trigger Point Pain | Myofascial Pain Syndrome of Neck | Myofascial Trigger Point SyndromePoland
-
Camilo Jose Cela UniversityCompletedMyofascial Pain Syndrome (MPS)Spain
-
Mahidol UniversityCompletedMyofascial Pain SyndromeThailand
-
Sobet AGLa Tour Hospital; Klinikum Klagenfurt am Wörthersee; Krankenhaus der Elisabethinen... and other collaboratorsRecruitingMyofascial Pain Syndrome - Lower Back | Myofascial Pain Syndrome - Neck | Myofascial Pain Syndrome - Tension HeadacheAustria, Switzerland
-
Green International UniversityCompleted
-
University of California, DavisNational Institutes of Health (NIH); National Center for Complementary and...Not yet recruitingChronic Low-back Pain (cLBP) | Myofascial Pain Syndrome (MPS)United States
-
Istanbul Training and Research HospitalCompletedMyofascial Pain Syndrome - Neck | Myofascial Pain of Upper Trapezius MuscleTurkey
-
Universidad Complutense de MadridRecruitingTrigger Point Pain, Myofascial | Myofascial Pain Syndrome of Neck | Myofacial PainSpain
Clinical Trials on Tele-rehabilitation (ET + Self-Myofascial Release)
-
Yeditepe UniversityNot yet recruiting
-
Investigación en Hemofilia y FisioterapiaCompleted
-
Investigación en Hemofilia y FisioterapiaCompleted
-
Istanbul University - CerrahpasaCompletedMobility Limitation | Pectoralis Minor Muscle Tension | Muscle Shortness | Forward Scapular Posture | Rounded Shoulder PostureTurkey
-
Sehat Medical ComplexCompletedPiriformis SyndromePakistan
-
Goethe UniversityCompletedFlexibility | Fascia | Self-Myofascial-Release | Passive Stiffness | Fascial SlidingGermany
-
Universitat Internacional de CatalunyaCompleted
-
Zeng ChanghaoPeople's Hospital of Zhengzhou UniversityNot yet recruiting
-
Copka SonpashanNot yet recruiting
-
Copka SonpashanNot yet recruiting