Effect of MET vs Neck Calliet Exercises on Neck Pain and Disability in Nurses

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-30
SponsorUniversity of Faisalabad

About this trial

This study compares the effectiveness of Muscle Energy Techniques (MET) and Neck Calliet Exercises in managing mechanical neck pain and associated disability due to trapezius trigger points among nurses. A total of 38 female nurses were randomly assigned to two intervention groups, each receiving therapy for four weeks. Pain, cervical range of motion, and disability outcomes were assessed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Female nurses

Between 18 and 30 years of age

Having mechanical neck discomfort that is confined to the cervical or bilateral scapular regions (pain level must be 3-5 VAS)

There must be at least one trigger point in trapezius muscle

Disqualifiers

A recent medical history including surgery on the shoulder or neck

Signs of myelopathy in the clinic or radiculopathy

Diagnosed Fibromyalgia syndrome, psychiatric problems

Pregnancy

Trial design

Design model

Parallel

Treatments tested in this trial

  • Muscle Energy Technique

    Behavioral

    Participants in this group received Muscle Energy Techniques targeting the upper trapezius trigger points. Treatment was provided 3 sessions per week for 4 weeks. Each session included post-isometric relaxation techniques with stretching, along with baseline TENS therapy.Participants performed Neck Calliet Exercises focusing on cervical flexion, extension, rotation, and lateral flexion. Exercises were done under supervision, 3 times per week for 4 weeks. All participants also received baseline TENS therapy.

  • Neck Calliet exercise

    Other intervention

    Neck Calliet exercise

Treatment groups

38 Participants
are divided into 2 treatment groups
Group A: MET GroupExperimental treatment 1 intervention
Group B: Calliet Exercise GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Pain Intensity Pain Intensity Pain intensity

Change in neck pain intensity was assessed using the Visual Analogue Scale (VAS), measured before and after 4 weeks of intervention.

Time frame
Baseline and 4 weeks
2

Functional Disability

Functional disability was evaluated using the Neck Disability Index (NDI) at baseline and after 4 weeks of treatment.

Time frame
Baseline and 4 weeks

Secondary outcomes

1

Cervical Range of Motion

Cervical range of motion (flexion, extension, rotation, lateral flexion) was measured using a universal goniometer pre- and post-intervention to assess changes in mobility.

Time frame
Baseline and 4 weeks

Other outcomes

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