New muscle technique aims to loosen neck knots and boost grip strength
NCT ID NCT07591259
First seen Jun 24, 2026 · Last updated Aug 21, 2026 · Updated 2 times
Summary
This study tests a hands-on technique called Integrated Neuromuscular Inhibition (INIMT) for people with painful muscle knots in the upper neck. 60 adults with trigger points will receive either INIMT plus standard therapy or standard therapy alone for four weeks. Researchers will measure changes in hand grip strength, pain, and wrist movement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Integrated Neuromuscular Inhibition Technique (INIMT) — a combination of pressure, stretching, and muscle energy methods
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease neck pain and improve hand strength in people with muscle trigger points.
- What could go wrong
- This is a small, early-stage study (60 people) comparing two physical therapy methods. Results may not apply to everyone, and the technique may not outperform standard care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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60 people
The number who actually took part.
- Started
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May 2026
- Finished
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Aug 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Subjects will be selected from out patient clinic of Delta University hospital, Dakahlia, Egypt. * Subjects aged between 18 and 55 years. * Their body mass index (BMI) were ranged from 18-30 kg/m2. * Subjects diagnosed as myofascial pain syndrome with a unilateral upper trapezius myofascial trigger point on the dominant side by a physician. * Subjects must have characteristics of trigger points: hardened, thickened taut bands in MPS patients. Contraction knots within taut muscle bands are pathognomonic features of MTrPs. Common features of the trigger point include the tender bands of muscles, taut band which could produce pain while pressing it directly or sometimes spontaneous, with this there was weak muscles, sensory motor dysfunctions, changes in motor control function and disruption of normal patterns of motor recruitments are seen. * Subjects from both genders. * The severity of pain on the visual analogue scale should be higher than two out of ten. * Patients will receive all standard medical treatment. Exclusion Criteria: * A history of any major neurological or musculoskeletal disorders, cardiovascular or respiratory diseases. * Neck pain due to cervical spine pathology. * Any history of cervical trauma, fractures or dislocations, carcinoma. * Uncooperative behavior, and unwillingness to participate. * Wrist problems (stiffness, fracture, operation or carpal tunnel syndrome).
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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out patient clinic of Delta University hospital
Gamasa, Egypt
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Other studies related to the condition(s) this trial covers.
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