ClinicalTrials.Veeva

Menu

Effectiveness Taif University P. O. Box 11099 Taif 21944 Effectiveness of Dry Needling in Management of Myofacial Trigger Point

T

Taif University

Status

Not yet enrolling

Conditions

Myofacial Trigger Points

Treatments

Other: usual physical therapy program
Other: Dry needling ,

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

myofascial pain syndrome is considered to be a chronic condition due to sensitive pressure points within the muscle recognized as trigger points

Generally the aim of this study will be :

  • To investigate the effectiveness of dry needling on trigger point in trapezius muscle
  • Evaluate the pain level before and after the applications of dry needling on trigger points
  • compare between the effects of dry needling and physical therapy exercise program

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Clinically active trigger point and expression of symptoms of neck pain in trapezius which had lasted for at least 3 months.
  • Having a pain level higher than 4 and lower than 8 on Visual Analogue Scale ( VAS )
  • Did not receive any other form of neck treatment during the previous month.

Exclusion criteria

  • Presence of cardiopulmonary disease , the application process requires the subject to be in prone position to expose the area of treatment, this position is un-preferable for cardiopulmonary patients
  • History of neck surgery
  • Trigger point treatment in the last 30 days
  • Any contraindications for dry needling such as local infection, skin disease ,severe postural disorder , tumor , rheumatoid arthritis, cervical spine stenosis and bilateral upper extremity symptoms
  • pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Intervention group
Experimental group
Treatment:
Other: Dry needling ,
Control group
Active Comparator group
Description:
Usual physical therapy protocol 4 sessions, two sessions per week each session will include a group of therapeutic exercises
Treatment:
Other: usual physical therapy program

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems