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Myofacial Trigger Points of Upper TrapeziusNCT07681661

Massage Gun vs Deep Friction Massage for Upper Trapezius Trigger Points

A study testing Massage Gun Therapy and Deep Friction Massage Group in people with Myofacial Trigger Points of Upper Trapezius, run by Ibadat International University, Islamabad at 1 site in Pakistan.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

This study compares the effectiveness of Massage Gun Therapy and Deep Friction Massage in individuals with upper trapezius myofascial trigger points. The interventions will be evaluated for their effects on pain intensity, pressure pain threshold, cervical range of motion, and neck disability. Read more about this study

Who is it for?
Ages 24 to 45 years
What is being tested?
Massage Gun Therapy and Deep Friction Massage Group
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
46 participants
Where
1 sitePakistan
Study dates
1 Jan 2026to 1 Sep 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 24 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Inclusion Criteria: Presence of active trigger points in the upper trapezius (confirmed by palpation, referred pain pattern, and pain reproduction)(travell and simson's method).

Moderate to severe pain (VAS>4/10). No prior treatment for neck/shoulder pain in past 4 weeks. Age 24-45 years (young adults according to WHO classification) Both genders Exclusion Criteria:History of cervical spine surgery or severe musculoskeletal pathology.

Neurological deficits. Systemic disease (e.g., rheumatoid arthritis, fibromyalgia). Recent trauma or fractures in the neck/shoulder region. Current pregnancy.

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Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

MUHAMMAD ASHAR RAFI, DPT, MS-NMPT contact

0092-308-3407837

ashar.rafi@uipt.iiui.edu.pk

Taila Nazir Malik, DPT contact

0092-336-5838844

tailamalik124@gmail.com

Pakistan1 site, 1 recruiting
  • Gulf Care Hospital, River gardens

    Islamabad

    Recruiting

Other trials in Pakistan

About this study

Official title: Effectiveness Of Massage Gun Therapy Versus Deep Friction Massage On Upper Trapezius Trigger Points

This study compares the effectiveness of Massage Gun Therapy and Deep Friction Massage in individuals with upper trapezius myofascial trigger points. The interventions will be evaluated for their effects on pain intensity, pressure pain threshold, cervical range of motion, and neck disability. The aim is to determine which treatment is more effective in reducing pain and improving functional outcomes.

Being tested
Massage Gun Therapy, Deep Friction Massage Group
Keywords
Myofascial Pain Syndromes Trigger Points Neck Pain Massage Musculoskeletal Pain Physical Therapy Modalities Rehabilitation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Massage Gun TherapyOther

    Massage Gun Therapy will be applied to the upper trapezius myofascial trigger point using a handheld percussive massage device. Participants will receive treatment for 5 minutes per session, three sessions per week for 2 weeks. The intervention aims to reduce pain, decrease muscle tension, improve pressure pain threshold, and enhance cervical range of motion and functional ability.

  • Deep Friction Massage GroupOther

    Deep Friction Massage will be applied manually over the upper trapezius myofascial trigger point using transverse friction techniques. Each session will last 5 minutes and will be administered three times per week for 2 weeks. The intervention aims to reduce pain, decrease muscle tightness, improve pressure pain threshold, increase cervical range of motion, and enhance functional ability.

Study groups in NCT07681661
Study groupRoleWhat they receive
Massage Gun Therapy groupActive comparatorParticipants in this group will receive Massage Gun Therapy applied to the upper trapezius myofascial trigger point according to a standardized treatment protocol. The intervention aims to reduce pain, decrease muscle tension, and improve cervical function.
Receives: Other: Massage Gun Therapy
Deep Friction Massage GroupSham comparatorParticipants in this group will receive Deep Friction Massage applied to the upper trapezius myofascial trigger point according to a standardized treatment protocol. The intervention aims to reduce pain, improve tissue mobility, and enhance cervical function.
Receives: Other: Deep Friction Massage Group

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Numaric Pain Rating scale(NPRS)

    Numeric Pain Rating Scale (NPRS): Pain intensity will be assessed using the Numeric Pain Rating Scale, an 11-point self-reported scale ranging from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst imaginable pain." Participants will rate their current level of pain, with higher scores indicating greater pain intensity.

    Measured: Baseline and post-intervention( From enrollment of first week and then to the end of 2 weeks)

Secondary outcomes (2)
  1. Cervical Range of Motion (CROM) Neck Disability Index (NDI)

    Cervical ROM (Inclinometer): Cervical range of motion will be measured using an inclinometer to assess neck movements including flexion, extension, lateral flexion, and rotation. Higher values indicate greater cervical mobility and improved neck function. Neck Disability Index(NDI):The Neck Disability Index (NDI) is a self-reported questionnaire used to assess neck-related functional disability. Scores range from 0 to 50, with higher scores indicating greater disability.

    Measured: Cervical ROM (Inclinometer): Baseline and after 2 weeks of intervention. Neck Disability Index(NDI):Baseline and after 2 weeks of intervention.

  2. Neck Disability Index (NDI)

    The Neck Disability Index (NDI) is a self-reported questionnaire used to assess neck-related functional disability. Scores range from 0 to 50, with higher scores indicating greater disability.

    Measured: Baseline and after 2 weeks of intervention.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Jul 2026
  2. Study start1 Jan 2026
  3. Primary completion1 Aug 2026 (estimated)
  4. Study completion1 Sep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Participant
Enrolment
46 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07681661
Sponsor's protocol ID
IIUI/RERC/ADT/2026/01/216
Status last verified
Jun 2026
First submitted
26 Jun 2026
Last updated
2 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing Massage Gun Therapy and Deep Friction Massage Group in people with Myofacial Trigger Points of Upper Trapezius, run by Ibadat International University, Islamabad at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 2 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact MUHAMMAD ASHAR RAFI, DPT, MS-NMPT (0092-308-3407837, ashar.rafi@uipt.iiui.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Numaric Pain Rating scale(NPRS) (time frame: Baseline and post-intervention( From enrollment of first week and then to the end of 2 weeks)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Jul 2026.

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