Skip to main content
Clinical Trials/NCT05939583
NCT05939583CompletedNot Applicable

Effect of Shock Wave Therapy on Upper Trapezius Trigger Points in Patients With Cervicogenic Headache. a Randomized Controlled Trial

October 6 University1 site in 1 country50 target enrollmentStarted: February 1, 2022Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
1
Primary Endpoint
Kinesiological EMG

Study Overview

Brief Summary

Control group will receive US, TENS, IR and exercises. The treatment group will receive the same program in addition to shock waves therapy. Patients will receive 3 sessions per week for 4 weeks.

Detailed Description

Control group will receive US, TENS, IR and exercises. The treatment group will receive the same program in addition to shock waves therapy. Patients will receive 3 sessions per week for 4 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
Double (Participant, Investigator)

Eligibility Criteria

Ages
20 Years to 40 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Fifty patients from both genders.
  • •Age ranging from 20 to 40 years.
  • •Referred by an orthopedist with a diagnosis of Mechanical neck dysfunction (MND) to physical therapy at the outpatient clinic of the Faculty of Physical Therapy, MTI University.

Exclusion Criteria

  • •All other disorders.

Arms & Interventions

Treatment Group

Experimental

The treatment group will receive US, TENS, IR and exercises in addition to shock waves therapy. Patients will receive 3 sessions per week for 4 weeks

Intervention: Shock Wave Therapy (Other)

Treatment Group

Experimental

The treatment group will receive US, TENS, IR and exercises in addition to shock waves therapy. Patients will receive 3 sessions per week for 4 weeks

Intervention: US, TENS, IR and exercises. (Other)

Control Group

Experimental

Control group will receive US, TENS, IR and exercises. Patients will receive 3 sessions per week for 4 weeks

Intervention: US, TENS, IR and exercises. (Other)

Outcomes

Primary Outcomes

Kinesiological EMG

Time Frame: 4 weeks

Analysis of root mean square for upper trapezius muscle functions.

Visual analogue scale

Time Frame: 4 weeks

Assess degree of pain from 1 (No Pain) to 10 (Severe Pain)

Neck disability index

Time Frame: 4 weeks

Assess degree of neck disability.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ahmed Magdy Alshimy

Lecturer Of Neurological Physical Therapy - Faculty Of Physical Therapy - October 6 University

October 6 University

Study Sites (1)

Loading locations...

Similar Trials