Comparing Efficacy of Dry Needling Combined with Passive Stretching and Muscle Energy Technique on Myofascial Trigger Points

ConditionNeck Pain
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-60
SponsorUniversity of Peradeniya

About this trial

The goal of this clinical trial is to assess and compare the efficacy of dry needling (minimally invasive treatment by using a tiny needle) combined with two types of stretching techniques in patients with neck pain for more than 3 months. The main questions it aims to answer are:

Which combination of treatment will 1.give faster relief of pain? 2.improve neck range of motion? and 3.improve disability level of a person with neck pain.

Participants who are interested will be selected according to eligibility criteria. Participants will be divided into two groups. Initially researcher will assess and interview the participants. Two groups will receive two different combinations of interventions. Pre and post measurements will be obtained and then treatment efficacy will be assessed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Presence of neck pain for at least 3 months or more

Presence of trigger points in the upper trapezius muscle, either unilaterally or bilaterally

Age between 18 and 60 years

Disqualifiers

Having an ongoing infection or fever

Presence of shoulder pathology, such as tendinopathy, impingement syndrome, capsulitis, or bursitis

History of direct trauma to the shoulder or neck

Immunosuppressed individuals (e.g., those with cancer)

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dry Needling

    Procedure/Surgery

    Treatment protocol: 1. Dry needling: Prone position, identify trigger points in upper trapezius, use Hong technique with 50mm/0.25 gauge needle, eliciting local twitch response. 2. Passive stretching: Supine position, cervical spine stretched just short of restriction, hold for 30s with 20s rest, repeat 3 times. 3. Muscle Energy Technique: Supine position, identify restriction barrier, move spine away from barrier, instruct patient to isometrically contract opposing movement (25% strength), hold for 7-10s, then stretch towards new barrier for 30s, repeat 3 times.

Treatment groups

46 Participants
are divided into 2 treatment groups
Group A: Treatment group 1Active comparator 1 intervention
Group B: Treatment group 2Other 1 intervention

Trial outcomes

Primary outcomes

1

Neck pain

Visual Analog Scale (VAS) 0: Represents the minimum value, such as "no pain" or "no discomfort." 100: Represents the maximum value, such as "worst pain imaginable" or "extreme discomfort.

Time frame
2 weeks

Secondary outcomes

1

Neck Range of Motion

Neck flexion, Extension, Side flexion to affected side, Side flexion to unaffected side, Rotation to affected side and Rotation to unaffected side

Time frame
2 weeks
2

Neck disability level

Neck Disability Index Structure: Contains 10 items, each scored on a 0-5 scale Scoring: Total score ranges from 0 to 50, Higher scores indicate greater disability.

Time frame
2 weeks

Other outcomes

Sponsors and contacts

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