ClinicalTrials.Veeva

Menu

Comparison Between Deep Dry Needling and Muscle Energy Technique on Chronic Non-specific Neck Pain Patients.

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Neck Pain

Treatments

Procedure: Deep dry needling
Procedure: Muscle energy technique
Procedure: Neck stability exercise

Study type

Interventional

Funder types

Other

Identifiers

NCT05730426
P.T.REC/012/003913

Details and patient eligibility

About

The goal of this clinical trial is to compare between applying deep dry needling and muscle energy technique in chronic non-specific neck pain patients. Researchers will compare between deep dry needling group, muscle energy technique group and control group to see if there are change in pain, range of motion or function.

Enrollment

66 patients

Sex

All

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18 and 40 years.
  2. Current neck pain.
  3. Presence of at least one or two trigger points .
  4. Patients are diagnosed and referred from orthopedist complaining from chronic neck pain for at least 12 weeks.
  5. No clinical treatment for neck pain within the past month.
  6. lacked a history of neck and shoulder myopathy, neuropathy, myelopathy and neck, torso and shoulder surgery.
  7. Patients with body mass index less than 30 kg/m2.

Exclusion criteria

  1. Patients outside the target range.
  2. Neck pain associated with vertigo.
  3. Osteoporosis.
  4. Diagnosed psychological disorders.
  5. Fibromyalgia syndrome.
  6. Vertebral fractures.
  7. Spinal stenosis.
  8. Tumors.
  9. Previous neck surgery.
  10. Red flags (night pain, severe muscle spasm, loss of involuntary weight, symptom mismatch).
  11. Physiotherapeutic treatment continued in the last 3 months. Any contraindications for deep dry needling such as anticoagulants, infections and bleeding.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

66 participants in 3 patient groups, including a placebo group

Group A
Active Comparator group
Description:
In addition to Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors), patients received deep dry needling on active trigger points in selected muscles (upper trapezius, levator scapulae, and sternocleidomastoid ), 3 sessions/week, for 4 weeks period.
Treatment:
Procedure: Deep dry needling
Group B
Active Comparator group
Description:
In addition to Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors), patients received muscle energy technique (post isometric relaxation) in selected muscles (upper trapezius, levator scapulae, and sternocleidomastoid ), 3 sessions/week, for 4 weeks period.
Treatment:
Procedure: Muscle energy technique
Group C
Placebo Comparator group
Description:
Patients receive Transcutaneous Electrical Nerve Stimulation (TENS) (typical,100 Hz, 20 mins), Infrared (7 mins), and Exercises (Cervical Stability Exercises through activation of deep neck flexors) , 3 sessions/week, for 4 weeks period.
Treatment:
Procedure: Neck stability exercise

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems