Comparative Impact of Integrated Neuromuscular Inhibition Technique, Dry Cupping and Dry Needling on Mechanical Neck Pain; A Randomized Controlled Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-40
SponsorBeni-Suef University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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 design

Design model

Parallel

Treatments tested in this trial

  • strengthening and stretching exercises

    Other intervention

    subjects will receive strengthening and stretching exercises

  • Integrated neuromuscular inhibition technique

    Other intervention

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

  • Dry Needling

    Device

    subjects in this group will receive Dry needling therapy, two sessions per week for four weeks

  • Dry cupping

    Device

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

Treatment groups

80 Participants
are divided into 4 treatment groups
Group A: Group AActive comparator 1 intervention
Group B: Group BExperimental treatment 1 intervention
Group C: Group CExperimental treatment 1 intervention
Group D: Group DExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

pain intensity

pain intensity will be measured by visual analogue scale

Time frame
0-4 weeks
2

pain pressure threshold

The pressure algometer will measure the pain pressure threshold

Time frame
0-4 weeks

Secondary outcomes

1

Neck Disability Index

The Neck Disability Index is a questionnaire to measure function

Time frame
0-4 weeks

Other outcomes

Sponsors and contacts

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