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Not yet recruitingNCT07063355Updated Jul 14, 2025

Stripping Massage Technique and Post-isometric Relaxation

An interventional study of Stripping Massage Technique: and Post-Isometric Relaxation (PIR) in Trapezius Myalgia, sponsored by Riphah International University. Not yet recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-07-14.

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

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
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Study summary

This randomized clinical trial investigates the synergistic effects of stripping massage and Post-Isometric Relaxation (PIR) on pain alleviation, ROM and functional movement improvement in individuals with Trapezius myalgia. A purposive sampling approach will select participants aged 18 and 50 years. A total of 44 patients will be taken, who will be randomly divided into two equal groups, each containing 22 patients. Group A will receive standard baseline management, supplemented with heating pad, active stretching, isometrics and ischemic compression, while Group B will receive the combined management (stripping massage + PIR) .

Read the detailed description

The study will assess pain intensity using NPRS, ROM using goniometer and neck disability or functional movement of neck using Neck Disability Index (NDI) at baseline and four weeks follow-up. Ethical approval and informed consent will ensure the study's integrity. The primary outcomes will focus on pain reduction and improved neck function, with secondary outcomes including trigger point severity and range of motion. Data analysis will utilize SPSS version 25. This study aims to provide valuable insights into the combined efficacy of stripping massage and PIR, ultimately informing evidence-based practice and enhancing patient outcomes in patients with trapezius myalgia.

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Conditions studied

  • Trapezius Myalgia

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Keywords

  • Pain
  • Range of Motion
  • Functional Movement
03

In context

Pain

2,219 studies on the registry are indexed under Pain; 917 are open to participants now.

This study's planned enrollment of 44 is below the median of 70 across 1,904 interventional studies indexed under Pain.

Browse Pain 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.

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Presenting with neck pain and stiffness
  • Experiencing tightness in the upper trapezius muscle
  • Having pain at rest, local twitch response or jump sign in upper trapezius
  • Patients having functional limitations while performing certain activities of everyday living.

Exclusion criteria

Exclusion Criteria:

  • Patients with an NPRS score of 3 or less.
  • Presence of structural abnormalities like torticollis or scoliosis.
  • Presence of skin disease on the back.
  • Having undergone upper limb surgery within the past year .
  • Participation in another clinical trial.
  • Severe psychiatric conditions that would impair participation or compliance
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
44 participants (estimated)

Study arms

  • Experimental
    Stripping Massage Technique

    Stripping Massage Technique: * The back of the neck and shoulder were uncovered. * Controlled and steady pressure was administered using the thumb along the entirety of the tense trapezius muscle, moving from origin to insertion and perpendicular to the muscle fibers, for approximately 3 minutes, twice weekly over a period of 4 weeks. * The pressure was progressively raised with each subsequent stroke, based on tolerance level.

    Other: Stripping Massage Technique:

  • Experimental
    Post isometric Relaxation

    Post-Isometric Relaxation (PIR): * During the PIR intervention, the patients rested in a supine position with their necks tilted to the side, away from the affected side, placing the upper trapezius muscle fibers in a stretched position. * A moderate isometric contraction, around 75% of the patient's maximum effort, was performed by the upper trapezius and maintained for 5 seconds, followed by a 3-second relaxation phase. * The therapist then gently mobilized the cervical spine to a new range of motion barrier. * This sequence was repeated four times per session

    Other: Post-Isometric Relaxation (PIR)

Interventions

  • OtherStripping Massage Technique:

    * The back of the neck and shoulder were uncovered. * Controlled and steady pressure was administered using the thumb along the entirety of the tense trapezius muscle, moving from origin to insertion and perpendicular to the muscle fibers, for approximately 3 minutes, twice weekly over a period of 4 weeks. * The pressure was progressively raised with each subsequent stroke, based on tolerance level.

  • OtherPost-Isometric Relaxation (PIR)

    * During the PIR intervention, the patients rested in a supine position with their necks tilted to the side, away from the affected side, placing the upper trapezius muscle fibers in a stretched position. * A moderate isometric contraction, around 75% of the patient's maximum effort, was performed by the upper trapezius and maintained for 5 seconds, followed by a 3-second relaxation phase. * The therapist then gently mobilized the cervical spine to a new range of motion barrier. * This sequence was repeated four times per session.

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What researchers measure

Primary outcomes

  1. NPRS

    The Numerical Pain Rating Scale (NPRS) is a numeric adaptation of the Visual Analogue Scale (VAS). In this version, the patient selects a number from 0 to 10 that best represents the intensity of their pain. This 11-point scale ranges from "no pain" to "worst pain imaginable," where 0 indicates no pain and 10 signifies extreme pain.

    Time frame: 4 weeks

  2. Universal Goniometer

    Range of motion (ROM) is a crucial parameter for assessing movement limitations. While clinicians commonly use goniometers to measure ROM, the accuracy of this method largely relies on the clinician's skill and experience.

    Time frame: 4 weeks

  3. NDI

    The NDI (Neck Disability Index) is a condition-specific, patient-completed questionnaire consisting of 10 items designed to evaluate pain and functional status, primarily used for reporting neck pain. Each item on the scale is scored from 0 to 5, with the total score interpreted as a percentage. A score of 0 points (0%) indicates no activity limitation, while a score of 50 points (100%) indicates complete activity limitation. The NDI is a reliable and valid questionnaire for neck pain patients, with interclass correlation coefficients ranging from 0.50 to 0.98

    Time frame: 4 Weeks

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Study locations

1 site
  • The Perfect Physiotherapy Clinic
    Muzaffargarh, Punjab Province 34200, Pakistan
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References and documents

Publications

  • Aras D, Al-Ihsan IM, Sutono E. The effectivity of trigger point dry needling in improving pain on people with upper trapezius myalgia. Enfermería Clínica. 2020;30:87-91.
  • Joshi A, Jawade S, Chitale N. Effectiveness of Myofascial Release (MFR) vs. High-Frequency Transcutaneous Electrical Nerve Stimulation (TENS) for Pain Relief and Functional Improvement in College Students With Trapezius Myalgia. Cureus. 2022 Oct 4;14(10):e29898. doi: 10.7759/cureus.29898. eCollection 2022 Oct. PubMed 36348914 ↗
  • Supornpun N, Rummaneethorn P, Nararatwanchai T, Saiwichai T, Chaichalotornkul S. Incobotulinum Toxin A with a One-year Long-lasting Effect for Trapezius Contouring and Superior Efficacy for the Treatment of Trapezius Myalgia. J Cutan Aesthet Surg. 2022 Apr-Jun;15(2):168-174. doi: 10.4103/JCAS.JCAS_68_21. PubMed 35965898 ↗
  • SAMIR SM, AMANY M, ABDELRAHMAN AC, SALWA FA. Effect of Passive Stretching Exercises Versus Post Isometric Relaxation Technique on Pain Intensity in Quadratus Lumborum Trigger Points on Lower Back Myofascial Pain Syndrome. The Medical Journal of Cairo University. 2024;91(12):1519-23.
  • Elagamawy MI, Elsayed WH, Zahran MR. Effect of Muscle Energy Technique versus Instrument-assisted Soft Tissue Mobilization in Upper Trapezius Myofascial Trigger Points. Egyptian Journal of Physical Therapy. 2023;16(1):7-16.
  • Albaker AB. Ischemic pressure vs. post-isometric relaxation for treatment of rhomboid latent myofascial trigger point: a systemic review. Eur Rev Med Pharmacol Sci. 2023 Jun;27(11):5031-5038. doi: 10.26355/eurrev_202306_32620. PubMed 37318477 ↗
  • El-Hafez HM, Hamdy HA, Takla MK, Ahmed SEB, Genedy AF, Abd El-Azeim ASS. Instrument-assisted soft tissue mobilisation versus stripping massage for upper trapezius myofascial trigger points. J Taibah Univ Med Sci. 2020 Mar 6;15(2):87-93. doi: 10.1016/j.jtumed.2020.01.006. eCollection 2020 Apr. PubMed 32368203 ↗
  • Junaid M, Yaqoob I, Shakil Ur Rehman S, Ghous M. Effects of post-isometric relaxation, myofascial trigger point release and routine physical therapy in management of acute mechanical neck pain: a randomized controlled trial. J Pak Med Assoc. 2020 Oct;70(10):1688-1692. doi: 10.5455/JPMA.15939. PubMed 33159734 ↗
  • Ghulam HS, Alqhtani RS, Alshahrani A, Ahmed H, Khan AR, Khan A. Efficacy of cervical mobilization with post-isometric relaxation in managing mechanical neck pain, ROM, and functional limitations associated with myofascial trigger points. Medicine (Baltimore). 2023 Dec 29;102(52):e36710. doi: 10.1097/MD.0000000000036710. PubMed 38206736 ↗
  • Fahmy EM, Ibrahim AR, Elabd AM. Ischemic Pressure vs Postisometric Relaxation for Treatment of Rhomboid Latent Myofascial Trigger Points: A Randomized, Blinded Clinical Trial. J Manipulative Physiol Ther. 2021 Feb;44(2):103-112. doi: 10.1016/j.jmpt.2020.07.005. PubMed 33715788 ↗

Individual participant data

Plan to share: No

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07063355
Lead sponsor
Riphah International University
Responsible party
Sponsor
First posted
Jul 14, 2025
Start date
Jul 24, 2025 (estimated)
Primary completion
Sep 20, 2025 (estimated)
Completion
Oct 20, 2025 (estimated)
Last update
Jul 14, 2025

Study contacts

Ayesha Mashal, MS student
Contact
ayeshamashal200@gmail.com
03057346060
Muzna Munir, PhD Scholar
Contact
muznafmh@gmail.com
03344265125
Muzna Munir, PhD*
principal investigator · Riphah International University

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2025. You cannot join it, but the record below documents what was studied.

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