NCT07027644

Brief Summary

The purpose of the study is to investigate the Synergistic Effects of the Integrated Neuromuscular Inhibition Technique and Dry Cupping Therapy on Pain Modulation and functional recovery on Myofascial Trigger Points of the upper trapezius

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
130

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 11, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

June 18, 2025

Completed
2 days until next milestone

Study Start

First participant enrolled

June 20, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 20, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 20, 2025

Completed
Last Updated

August 7, 2025

Status Verified

August 1, 2025

Enrollment Period

3 months

First QC Date

June 11, 2025

Last Update Submit

August 6, 2025

Conditions

Keywords

Dry cuppingIntegrated Neuromuscular Inhibition technique

Outcome Measures

Primary Outcomes (2)

  • Pain intensity

    pain intensity will be measured by visual analogue scale

    0-4 weeks

  • pain pressure threshold

    The pressure algometer will measure the pain pressure threshold

    0-4 weeks

Secondary Outcomes (1)

  • Neck Disability Index

    0-4 weeks

Study Arms (4)

stretching and strengthening group

PLACEBO COMPARATOR

Patients in this group will receive stretching and strengthening exercises, two sessions per week for four weeks

Other: stretching and strengthening exercises

Integrated Neuromuscular Inhibition Group

EXPERIMENTAL

Patients in this group will receive the Integrated Neuromuscular Inhibition technique three sessions per week for four weeks

Other: Integrated Neuromuscular Inhibition Technique

Dry cupping group

EXPERIMENTAL

Patients in this group will receive Dry cupping therapy, two sessions per week for four weeks

Device: Dry Cupping Therapy

Combined treatment group

EXPERIMENTAL

Patients in this group will receive Dry cupping therapy, two sessions per week for four weeks, the Integrated Neuromuscular Inhibition technique, three sessions per week for four weeks plus stretching and strengthening exercises, two sessions per week for four weeks

Other: combined integrated neuromuscular inhibition, dry cupping and stretching and strengthening exercises

Interventions

The patients receive dry cupping therapy for 10 min on the marked trigger point using a plastic set with a hand vacuum pump

Dry cupping group

The patients receive the Integrated Neuromuscular Inhibition Technique, which consists of ischemic compression, strain-counterstrain, and muscle energy techniques.

Integrated Neuromuscular Inhibition Group

The patients receive stretching and strengthening exercises

stretching and strengthening group

the patients recive all the three interventions

Combined treatment group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Medically competent men and women will be included They had chronic MTrPs in the upper trapezius for more than 6 months Diagnostic criteria of being a tight band with a palpable nodule and distant pain when subjected to pressure

You may not qualify if:

  • subjects with previous neck or shoulder pathology (e.g., fracture, sur¬gery, inflammatory and infectious diseases), cervical disc pathology, systemic disorder, fibromyalgia, those who underwent physical therapy for at least the previous 3 months

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physical Therapy

Giza, Egypt

RECRUITING

Central Study Contacts

Dina Al-Amir Mohamed, Lecturer

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Lecturer

Study Record Dates

First Submitted

June 11, 2025

First Posted

June 18, 2025

Study Start

June 20, 2025

Primary Completion

September 20, 2025

Study Completion

September 20, 2025

Last Updated

August 7, 2025

Record last verified: 2025-08

Locations