Mechanical Neck PainNCT07711041
Comparative Impact of Integrated Neuromuscular Inhibition Technique, Dry Cupping and Dry Needling on Mechanical Neck Pain; A Randomized Controlled Trial
A study testing strengthening and stretching exercises, Integrated neuromuscular inhibition technique and Dry Needling in people with Mechanical Neck Pain and Dry Needling Technique, run by Beni-Suef University at 1 site in Egypt.
Trial summary
This study ill include four treatment groups. Group A who will receive traditional physical therapy, group B who will receive INIT plus traditional physical therapy , group C who will receive dry cupping therapy plus traditional physical therapy or group D will receive Dry needling therapy plus traditional physical… Read more about this study
- Who is it for?
- Ages 18 to 40 years
- Conditions the study is for
- Mechanical Neck Pain, Dry Needling Technique, Dry Cupping Technique
- What is being tested?
- strengthening and stretching exercises, Integrated neuromuscular inhibition technique and Dry Needling
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteEgypt
- Study dates
- Jul 2026to May 2027
- 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 18 to 40 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- 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
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Egypt1 site, 1 recruiting
- Recruiting
Faculty of Physical Therapy
Giza
Dina Al-Amir Mohamed, Lecturer, 002+01229370053, dinaalamir@pt.bsu.edu.eg
About this study
This study ill include four treatment groups. Group A who will receive traditional physical therapy, group B who will receive INIT plus traditional physical therapy , group C who will receive dry cupping therapy plus traditional physical therapy or group D will receive Dry needling therapy plus traditional physical therapy . All groups completed 4 weeks of intervention.
- Being tested
- strengthening and stretching exercises, Integrated neuromuscular inhibition technique, Dry Needling, Dry cupping
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
strengthening and stretching exercisesOther
subjects will receive strengthening and stretching exercises
Integrated neuromuscular inhibition techniqueOther
The subjects receive the Integrated Neuromuscular Inhibition Technique, which consists of ischemic compression, strain-counterstrain, and muscle energy techniques.
Dry NeedlingDevice
subjects in this group will receive Dry needling therapy, two sessions per week for four weeks
Dry cuppingDevice
Patients in this group will receive Dry cupping therapy, two sessions per week for four weeks
| Study group | Role | What they receive |
|---|---|---|
| Group A | Active comparator | Not described Receives: Other: strengthening and stretching exercises |
| Group B | Experimental | Not described Receives: Other: Integrated neuromuscular inhibition technique |
| Group C | Experimental | Not described Receives: Device: Dry cupping |
| Group D | Experimental | Not described Receives: Device: Dry Needling |
What is being measured
The primary outcome is the main question the study is designed to answer.
pain intensity
pain intensity will be measured by visual analogue scale
Measured: 0-4 weeks
pain pressure threshold
The pressure algometer will measure the pain pressure threshold
Measured: 0-4 weeks
Secondary outcomes (1)
Neck Disability Index
The Neck Disability Index is a questionnaire to measure function
Measured: 0-4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Jul 2026
- Study startJul 2026 (estimated)
- Primary completionFeb 2027 (estimated)
- Study completionMay 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Mechanical Neck PainStudies of the same condition, open and under way.
- More trials run by Beni-Suef UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 80 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Beni-Suef University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Dina Al-Amir Mohamed Hussein, Beni-Suef University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07711041
- Sponsor's protocol ID
- Beni-Suef005
- Status last verified
- Jul 2026
- First submitted
- 14 Jul 2026
- Last updated
- 17 Jul 2026
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 17 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Impact of Integrated Neuromuscular Inhibition Technique, Dry Cupping and Dry Needling on Mechanical Neck Pain; A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT07711041
- Acronym / sponsor ID
- Beni-Suef005
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 80 participants (estimated)
- Lead sponsor
- Beni-Suef UniversityUniversity, hospital or other
- Study start
- Jul 2026 (estimated)
- Primary completion
- Feb 2027 (estimated)
- Study completion
- May 2027 (estimated)
- First posted
- 17 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study ill include four treatment groups. Group A who will receive traditional physical therapy, group B who will receive INIT plus traditional physical therapy , group C who will receive dry cupping therapy plus traditional physical therapy or group D will receive Dry needling therapy plus traditional physical therapy . All groups completed 4 weeks of intervention.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Group A | Active comparator | Other: strengthening and stretching exercises |
| Group B | Experimental | Other: Integrated neuromuscular inhibition technique |
| Group C | Experimental | Device: Dry cupping |
| Group D | Experimental | Device: Dry Needling |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (1 listed)
- 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
Key exclusion criteria (1 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| strengthening and stretching exercisessubjects will receive strengthening and stretching exercises | Other | Group A |
| Integrated neuromuscular inhibition techniqueThe subjects receive the Integrated Neuromuscular Inhibition Technique, which consists of ischemic compression, strain-counterstrain, and muscle energy techniques. | Other | Group B |
| Dry Needlingsubjects in this group will receive Dry needling therapy, two sessions per week for four weeks | Device | Group D |
| Dry cuppingPatients in this group will receive Dry cupping therapy, two sessions per week for four weeks | Device | Group C |
Primary outcome
pain intensity
Time frame: 0-4 weeks
pain intensity will be measured by visual analogue scale
pain pressure threshold
Time frame: 0-4 weeks
The pressure algometer will measure the pain pressure threshold
1 secondary outcome
Neck Disability Index
Time frame: 0-4 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 17 Jul 2026.
- Individual participant dataSharing planned: Undecided
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The Association Between Smartphone Overuse and Mechanical Neck Pain Among Galala University Students
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing strengthening and stretching exercises, Integrated neuromuscular inhibition technique and Dry Needling in people with Mechanical Neck Pain and Dry Needling Technique, run by Beni-Suef University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. 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 17 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 Egypt. 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. 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 Dina Al-Amir Mohamed, Lecturer (002+01229370053, dinaalamir@pt.bsu.edu.eg), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
pain intensity (time frame: 0-4 weeks). The study lists 2 primary outcomes in all. 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 17 Jul 2026.