Tele-rehabilitation for rhomboid trigger points in myofascial pain syndrome
Official title: Effectiveness of Tele-Rehabilitation in Managing Rhomboid Trigger Points in Patients With Myofascial Pain Syndrome
Run by Riphah International University · NCT07573527 · Data updated 2026-11-12
This trial tests whether tele-rehabilitation with self-myofascial release and exercise can reduce neck pain and improve function in adults with rhomboid trigger points.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 35 Years |
| Sex | All |
| Enrollment | 36 (estimated) |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Karachi, Sindh) |
| Status | Recruiting |
| Started | August 5, 2026 |
| Main results expected | December 2026 |
| Study ends | February 2027 |
| Registry record updated | August 6, 2026 |
| Trial ID | NCT07573527 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18-35 with active rhomboid trigger points and neck/upper back pain, who have internet access and meet the inclusion criteria.
✕Probably not a fit
Patients without active trigger points or those with exclusion criteria may not experience benefit from this approach.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study compares tele-rehabilitation that combines guided self-myofascial release and exercise with conventional myofascial release treatment for people with myofascial pain syndrome affecting the rhomboids. Participants receive remote, guided therapy aimed at reducing pain, increasing range of motion, and decreasing neck disability. The trial is conducted at Jinnah Postgraduate Medical Center in Karachi and is led by Riphah International University. Eligible adults are 18 to 35 with active rhomboid trigger points, neck and upper back pain, and access to internet-enabled devices. Exclusion criteria include inflammatory or neurological conditions, cervical tumors, scoliosis or torticollis, spinal injuries, recent analgesic or muscle relaxant use, or other major comorbidities.
Why it matters
Potential benefit: If successful, patients may experience reduced pain and improved neck function with a convenient remote therapy option.
How similar studies have gone: Tele-rehabilitation and self-myofascial release approaches have shown promise in related musculoskeletal conditions, though this exact combination for rhomboid trigger points is novel in this setting.
Who can join: the full rules
Show full inclusion / exclusion criteria
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.
Where it's running
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Jpmc
Karachi, Sindh, Pakistan Recruiting
Study contacts
- Principal investigator: Maria khalid, MSOMPT — Riphah International University
- Study coordinator: Maria Khalid, MSOMPT
- Email: maria.khaild@riphah.edu.pk
- Phone: 03315369768
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Focused Shockwave Therapy for neck and shoulder pain
A 60-person study tests whether focused shockwave therapy can reduce pain and improve function in adults with chronic neck and shoulder myofascial pain compared with a home exercise program.
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Three treatment options for myofascial back pain
This trial will test whether dry needling, shock wave therapy (ESWT), or pulsed radiofrequency (PRF) reduces pain and improves function in adults 18–65 with chronic myofascial back pain.
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Reflex therapy and dry needling for jaw muscle and joint pain
This trial will try adding dry needling to standard rehabilitation to see if adults with functional temporomandibular (jaw) pain get less pain, better jaw movement, and improved quality of life.
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PRP pharmacopuncture for chronic neck pain from upper trapezius myofascial syndrome
This trial will try a single Platelet‑Rich Plasma (PRP) pharmacopuncture injection to see if it reduces chronic neck pain and improves function in adults with upper trapezius myofascial pain.
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Effects of Different Myofascial Release Techniques on Function in Chronic Neck Pain
This trial tests whether manual or self-applied myofascial release, in addition to standard therapy and exercise, can improve function and reduce pain in adults with chronic non-specific neck pain.
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Comparing physical therapy methods to improve head‑neck alignment in neck myofascial pain
This will test whether different physical therapy treatments—dry needling, trigger‑point therapy, Maitland mobilizations, TENS, and ultrasound—can improve head‑neck alignment and reduce symptoms in adults 20–40 with cervical myofascial pain.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.