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Effect of Shockwave Therapy on Cervical Myofascial Syndrome in Lactating Women

Effect of Shockwave Therapy on Cervical Myofascial Pain Syndrome in Lactating Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05878821
Enrollment
30
Registered
2023-05-26
Start date
2023-08-25
Completion date
2023-09-25
Last updated
2024-03-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Myofascial Pain Syndrome

Brief summary

the aim of the study is to determine the effect of shockwave therapy on cervical myofascial pain syndrome in lactating women

Detailed description

Neck and shoulder pain was 73,1%,one fourth of which occurred after birth.the most common area was the superior part of the trapezius.the symptoms of patients are pain, stiffness and limited range of motion (ROM).

Interventions

DEVICEShockwave

Shockwave therapy session once a week for month 1000shock per session

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Double masking

Intervention model description

Two groups,one group will be treated by shockwave therapy and postural correction exercise and other group will be treated by postural correction exercise

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Multipara two months after labor. * number of parity not more than 3. * age range 25\_35.BMI less than 35 Kg/m2

Exclusion criteria

* Diabetic women * Women with malignancy * Neck pain from other conditions such as(spinal * instability, spinal fracture, spinal cord compression,inflammatory disease, spinal infection, congenital postural deformity

Design outcomes

Primary

MeasureTime frameDescription
Visual analogue scale4 weeksPain level will be assessed for both groups (A&B) before and after treatment program by using (VAS). scores are based on self-reported measures of symptoms that are recorded with a single hand written mark placed at one point along the length of a10 cm line.0 cm means no pain.10cm means maximum pain.
Pressure Algometer4 weeksPain threshold for each woman in both groups (A&B) will be measured before and after the treatment program by using Pressure Algometer . The pressure pain threshold measurements for trapezius will be performed at mid-way between the seventh cervical vertebrae and acromial angle in limited area in the second and third quadrants (Barbero et al.' 2013).

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026