CClinicalTrials.gg
RecruitingNCT07573527Updated Aug 6, 2026

Effectiveness of Tele-Rehabilitation in Managing Rhomboid Trigger Points in Patients With Myofascial Pain Syndrome

An interventional study of Tele-rehabilitation (ET + Self-Myofascial Release) and Conventional Myofascial Release Treatment in Myofascial Pain Syndrome, sponsored by Riphah International University. Recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 35 Years. Per ClinicalTrials.gov, last updated 2026-08-06.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
36
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
All
01

Study summary

This randomized controlled trial aims to assess the effectiveness of tele-rehabilitation, including self-myofascial release and exercise therapy, in reducing pain, improving functional range of motion, and decreasing neck disability in patients with rhomboid trigger points associated with myofascial pain syndrome.

Read the 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.

02

Conditions studied

  • Myofascial Pain Syndrome

Keywords

  • Tele-rehabilitation
  • Myofascial Release
  • Self-Myofascial Release,
  • Rhomboid Trigger Points
  • Neck Pain
  • Postural Correction
  • cervical retraction
  • scapular retraction
  • Upper Trapezius & Levator Scapulae Stretch
03

In context

Myofascial Pain Syndromes

1,136 studies on the registry are indexed under Myofascial Pain Syndromes; 137 are open to participants now.

This study's planned enrollment of 36 is below the median of 60 across 931 interventional studies indexed under Myofascial Pain Syndromes.

Browse Myofascial Pain Syndromes studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,133 studies on the registry; 633 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
36 participants (estimated)

Study arms

  • Experimental
    Tele-rehabilitation (Exercise Therapy + Self-Myofascial Release)

    1. Self-Myofascial Release: Using a tennis ball against the wall targeting rhomboid region (5 mintues in total). 2. Stretching Exercises: Upper trapezius and levator scapulae stretch (30 seconds hold × 5 repetitions). 3. Postural correction Exercises: cervical retraction and shoulder blade squeezing /retraction ( 5 repetitions). 4. Postural and ergonomic education . 5. Mode of Delivery: Live/video-guided tele-rehabilitation sessions.

    Other: Tele-rehabilitation (ET + Self-Myofascial Release)

  • Other
    Conventional Myofascial Release Treatment

    1. Manual Myofascial Release: Therapist performe myofascial release on rhomboid trigger points.( 5 mintues in total) 2. Stretching Exercises: Upper trapezius and levator scapulae stretch (30 seconds hold × 5 repetitions). 3. Postural correction Exercises: cervical retraction and shoulder blade squeezing /retraction ( 5 repetitions). 4. Postural and ergonomic education . 5. Mode of Delivery: In hospital treatment.

    Other: Conventional Myofascial Release Treatment

Interventions

  • OtherTele-rehabilitation (ET + Self-Myofascial Release)

    1. Self-Myofascial Release: Using a tennis ball against the wall targeting rhomboid region (5 mintues in total). 2. Stretching Exercises: Upper trapezius and levator scapulae stretch (30 seconds hold × 5 repetitions). 3. Postural correction Exercises: cervical retraction and shoulder blade squeezing /retraction ( 5 repetitions). 4. Postural and ergonomic education . 5. Mode of Delivery: Live/video-guided tele-rehabilitation sessions.

  • OtherConventional Myofascial Release Treatment

    1. Manual Myofascial Release: Therapist performe myofascial release on rhomboid trigger points.( 5 mintues in total) 2. Stretching Exercises: Upper trapezius and levator scapulae stretch (30 seconds hold × 5 repetitions). 3. Postural correction Exercises: cervical retraction and shoulder blade squeezing /retraction ( 5 repetitions). 4. Postural and ergonomic education .

06

What researchers measure

Primary outcomes

  1. Inclinometer for functional range of motion

    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.

    Time frame: 2 weeks

  2. Numeric Pain Rating Scale (NPRS)

    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

    Time frame: 2 weeks

  3. Neck Disability Index (NDI)

    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.

    Time frame: 2 weeks

07

Study locations

1 of 1 sites recruiting
  • JPMC
    Karachi, Sindh, Pakistan
    • maria khalid, MSOMPT · Contact · maria.khalid@riphah.edu.pk · 03315369768
    • Rameeqa Aamir, MSOMPT* · Contact
    • Rameeqa Aamir, MSOMPT* · Principal investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07573527
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
May 7, 2026
Start date
Aug 5, 2026
Primary completion
Dec 2026 (estimated)
Completion
Feb 2027 (estimated)
Last update
Aug 6, 2026

Study contacts

Maria Khalid, MSOMPT
Contact
maria.khaild@riphah.edu.pk
03315369768
Maria khalid, MSOMPT
principal investigator · Riphah International University

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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